Next Article in Journal
Postoperative Administration of the Acetylcholinesterase Inhibitor, Donepezil, Interferes with Bone Healing and Implant Osseointegration in a Rat Model
Previous Article in Journal
Regulation of p27Kip1 and p57Kip2 Functions by Natural Polyphenols
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Biomolecules
Volume 10
Issue 9
10.3390/biom10091317
biomolecules-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Nephroprotective Effect of Pleurotus ostreatus and Agaricus bisporus Extracts and Carvedilol on Ethylene Glycol-Induced Urolithiasis: Roles of NF-κB, p53, Bcl-2, Bax and Bak

by
Osama M. Ahmed
1,*,
Hossam Ebaid
2,3,*,
El-Shaymaa El-Nahass
4,
Mahmoud Ragab
5,6 and
Ibrahim M. Alhazza
2
1
Physiology Division, Zoology Department, Faculty of Science, Beni-Suef University, Beni-Suef P.O. 62521, Egypt
2
Department of Zoology, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia
3
Department of Zoology, Faculty of Science, El-Minia University, Minya P.O. 61519, Egypt
4
Department of Pathology, Faculty of Veterinary Medicine, Beni-Suef University, Beni-Suef P.O. 62521, Egypt
5
Sohag General Hospital, Sohag 42511, Egypt
6
The Scientific Office of Pharma Net Egypt Pharmaceutical Company, Nasr City, Cairo 11371, Egypt
*
Authors to whom correspondence should be addressed.
Biomolecules 2020, 10(9), 1317; https://doi.org/10.3390/biom10091317
Submission received: 21 July 2020 / Revised: 2 September 2020 / Accepted: 5 September 2020 / Published: 14 September 2020
Browse Figures
Versions Notes

Abstract

:
This study was designed to assess the nephroprotective effects of Pleurotus ostreatus and Agaricus bisporus aqueous extracts and carvedilol on hyperoxaluria-induced urolithiasis and to scrutinize the possible roles of NF-κB, p53, Bcl-2, Bax and Bak. Phytochemical screening and GC-MS analysis of mushrooms’ aqueous extracts were also performed and revealed the presence of multiple antioxidant and anti-inflammatory components. Hyperoxaluria was induced in Wistar rats through the addition of 0.75% (v/v) ethylene glycol in drinking water for nine weeks. The ethylene glycol-administered rats were orally treated with Pleurotus ostreatus and Agaricus bisporus aqueous extracts (100 mg/kg) and carvedilol (30 mg/kg) daily during the last seven weeks. The study showed that Pleurotus ostreatus, Agaricus bisporus and carvedilol all successfully inhibited ethylene glycol-induced histological perturbations and the elevation of serum creatinine, serum urea, serum and urinary uric acid, serum, urinary and kidney oxalate, urine specific gravity, kidney calcium, kidney NF-κB, NF-κB p65, NF-κB p50, p53, Bax and Bak expressions as well as serum TNF-α and IL-1β levels. Moreover, the treatment decreased the reduction in urinary creatinine, urinary urea, ratios of urinary creatinine to serum creatinine and urinary urea to serum urea, Fex Urea and Bcl-2 expression in kidney. In conclusion, although Pleurotus ostreatus and Agaricus bisporus extracts and carvedilol all significantly inhibited the progression of nephrolithiasis and showed nephroprotective effects against ethylene glycol-induced kidney dysfunction, Pleurotus ostreatus and Agaricus bisporus seemed to be more effective than carvedilol. Moreover, the nephroprotective effects may be mediated via affecting NF-κB activation, extrinsic apoptosis and intrinsic apoptosis pathways.

1. Introduction

Urolithiasis is a urinary stone disease involving the calcifications in the kidney [1]. In addition, urolithiasis is a very painful and the third common disorder of urinary system [2,3]. Epidemiological studies have revealed that the majority of stones are commonly composed of calcium oxalate (CaOx) [4,5]. The risk of developing urolithiasis appears to be associated with a multitude of genetic, physiological and nutritional disorders, ranging from general hyperoxaluria to obesity [6].
Hyperoxaluria describes the occurrence of high oxalate concentrations in urine. Although hyperoxaluria is most often simply a result of excess dietary oxalate intake, with research suggesting that dietary oxalate accounts for as much as 50% of the total urinary oxalate, there is also a genetic form of the condition, known as primary hyperoxaluria [7,8,9,10,11]. Hyperoxaluria is, in turn, an important risk factor for urolithiasis and more than 80% of the uroliths consist of CaOx, either alone or mixed with calcium phosphate [12,13,14].
The exposure of the renal epithelial cells to high levels of oxalate and crystals of CaOx/calcium phosphate generates excess reactive oxygen species (ROS), causing injury and inflammation [15]. Epithelial cell injury facilitates the events of CaOx crystal nucleation and aggregation and promotes crystal retention in renal tubules, which is crucial for subsequent stone development [5,16,17,18]. In humans, the accumulation of oxalate causes a number of pathological conditions, which include hyperoxaluria, the formation of CaOx kidney stones (urolithiasis) and renal failure [19]. The regulation of the genes that encode proteins involved in immune and inflammatory responses (i.e., cytokines, chemokines, growth factor immune receptors, cellular ligands and adhesion molecules) is controlled by nuclear factor-kappa B (NF-κB) [20]. Thus, NF-κB plays a pivotal role in control of the inflammation in hyperoxaluria and obstructive nephropathy [21]. On the other hand, it was speculated that hyperoxaluria induced apoptosis in renal tubular epithelial cells as an end stage of crystal–cell interaction [22]. The target genes involved in apoptosis are induced after activation of p53 upon DNA damage [23]. Bcl-2, which is an integral mitochondrial membrane protein, blocks apoptosis induced by a wide array of death signals [24].
Although different treatment strategies for urolithiasis have evolved over the years, discrepancies exist concerning the clinical indications and the efficacy of each of these treatment options [25]. Current medical approaches for therapies of urolithiasis are based on carefully constructed and rational modifications of urinary biochemistry as well as physical chemistry to minimize stone secondary risks rather than etiologies. Thus, the search for product of natural sources that prevent the causes and progress or even the recurrence of nephrolithiasis has attracted many researchers [26,27,28,29].
Mushrooms have long had a role as a branch of alternative medicine [30] and as functional diets [31]. In particular, Pleurotus ostreatus (P. ostreatus) has been confirmed to have medicinal effects, spanning anti-carcinogenic, anti-hypercholesterolemic, anti-inflammatory, anti-oxidative, immuno-stimulating and anti-viral properties and ability to regulate blood lipid and glucose levels [32,33,34,35,36]. Another important medicinal mushroom is Agaricus bisporus (A. bisporus), which has been demonstrated to possess various valuable biological properties including anti-aromatase, anti-inflammatory, antitumor, antimicrobial, antioxidant and immunomodulatory activities [37,38,39,40].
Carvedilol, meanwhile, is a multifunctional neurohormonal antagonist that has been shown to provide greater benefit than classical β-blockers because of its antioxidant effects, which work in synergy with its nonspecific α1- and β-blocking actions [41]. It has also been reported that carvedilol has anti-inflammatory activities in addition to its antioxidant properties [42]. Carvedilol is of interest in this study since it has been shown to protect against nephrotoxicity induced by ferric nitrilotriacetate in rats [43] as well as to improve renal function by ameliorating renal ischemia-reperfusion injury [44]. Finally, it has been speculated that carvedilol is a very promising candidate for clinical trials in future as a nephroprotector in patients treated with the nephrotoxic drug, cisplatin [45].
In conductance with the previous literature, the present study aimed to assess the protective effects of P. ostreatus and A. bisporus aqueous extracts and carvedilol on hyperoxaluria-induced nephrolithiasis in Wistar rats and to elucidate the probable implications of NF-κB, NF-κB p65, NF-κB p50, p53, Bcl-2, Bax and Bak in their mechanisms of action.

2. Materials and Methods

2.1. Animals and Housing

Male Wistar rats of weight ranging from 115 to 140 g were obtained from the National Research Center (NRC), El-Tahrir Street, Dokki, Egypt. To exclude any intercurrent infections, rats were kept overseen for ten days before starting the experiment. The rats were housed in cages with good aerated covers at room temperature (20–25 °C) and 12-h light/dark cycle, supplied with excess food (balanced standard diet) and water ad libitum. All animal procedures were approved by Experimental Animal Ethics Committee for use and care of animals, Faculty of Science, Beni-Suef University, Egypt (Ethical Approval number: BSU/FS/2015/19). All efforts were done to minimize the pain, discomfort and suffering of animals.

2.2. Mushrooms

Oyster mushroom (P. ostreatus) and button mushroom (A. bisporus) (Figure 1 and Figure S1) were supplied from Agriculture Research Center, Giza, Egypt. The two mushrooms were identified by Dr. Fathy Ragab, Food Technology Research Institute, Agriculture Research Center, Giza, Egypt. Fruiting bodies were cut into small pieces and dried at shaded good aerated area.

2.3. Preliminary Phytochemical Screening of Mushrooms

The tests, performed according to Claus [46], were used to detect different active principles including glycosides, carbohydrates, alkaloids, flavonoids, saponins, tannins, resins, unsaturated sterols and triterpenes.

2.4. Preparation of Mushroom Aqueous Extracts

The dried fruiting bodies of P. ostreatus and A. bisporus were roughly cut and ground with an electric grinder. P. ostreatus and A. bisporus aqueous extracts were prepared by adding certain weight of the powdered mushroom to certain volume of boiling distilled water (2% w/v) and was soaked for 15 min then filtrated. The resulting filtrates of P. ostreatus and A. bisporus were orally given to the rats at dose level of 100 mg/kilogram body weight (kg b.w.) daily by oral gavage for seven weeks. The doses of P. ostreatus and A. bisporus were orally administered, in the present study, according to the doses used by previous publications [47,48].

2.5. Gas Chromatography–Mass Spectrometry (GC-MS) Analysis of Aqueous extracts

P. ostreatus and A. bisporus aqueous extracts were frozen at −80 °C and powdered by drying in a lyophilizer. Then, chemical analysis was performed in the Central Laboratory of the Faculty of Postgraduate Studies for Advanced Sciences, Beni-Suef University, Egypt by using Gas Chromatography (GC) system 7890A/5975C Inert Mass Spectrometry (MS) with Triple Axis Detector, Ailent Technologies, Germany. Samples were injected in a splitless mode. The oven temperature program during analysis was as follows: 110 °C for 1 min, then 6 °C/min to 280 °C for 10 min. The equilibration time and the run time were 5 min and 39.333 min, respectively. The injection volume was 1 μL. Temperatures of the injector, MS source and MS Quad were 250 °C, 230 °C and 150 °C, respectively. Agilent 19091S-433: 2330.46415 HP-5MS 5% Phenyl Methyl Silox (30 m × 250 µm × 0.25 µm) column was used. Helium was used as a carrier at a flow rate of 1 mL/min. The constituents were recognized by comparing their mass spectra with the spectra of derivatives in the Library Search Report (C:\Database\NIST11.L).
The representation and interpretation of GC-MS results were revised by Prof. Dr. Sameh F. AbouZid, Pharmacognosy Department, Faculty of Pharmacy, Beni-Suef University, Beni-Suef, Egypt, Dr. Hassan M. Abdel-Aziz, Associate professor of Organic Chemistry, Department of Chemistry, Faculty of Science, Beni-Suef University, Egypt and Dr. Mai Raslan, Associate Professor of Biotechnology, Biotechnology and Life Sciences Department, Faculty of Postgraduate Studies for Advanced Sciences, Beni-Suef University, Egypt.

2.6. Preparation of Carvedilol Dose

The dose of carvedilol was prepared by dissolving 6 tablets of the drug (25 mg) in 25 mL distilled water (30 mg/5 mL) and was supplied to the rats by oral gavage at dose level of 30 mg (dissolved in 5 mL distilled water)/kg b.w. [49] daily for seven weeks. Carvedilol was obtained from Acapy Pharmaceutical Company, Egypt.

2.7. Induction of Hyperoxaluria

It has been shown by many researchers that a model of hyperoxaluria and urolithiasis in rats can be induced by ethylene glycol [50,51,52]. Hyperoxaluria, in the present study, was induced by adding ethylene glycol to the drinking water (0.75% v/v) [53,54] for 28 days. Ethylene glycol was purchased from S.D. Fine-Chem Limited, Mumbai, India.

2.8. Animal Grouping

After accommodation period, rats were allocated into five groups of six rats each as follow:
Group 1 (normal control) was supplied with tap water as a drinking water for nine weeks ad libitum for nine weeks and was given the equivalent volume of the vehicle (distilled water) 5 mL/kg b.w. daily by oral gavage during the last seven weeks.
Group 2 (ethylene glycol group) received ethylene glycol in drinking tap water (0.75% v/v) ad libitum for nine weeks and was supplemented with the equivalent volume of the vehicle (distilled water) 5 mL/kg b.w. daily by oral gavage during the last seven weeks.
Group 3 (ethylene glycol and aqueous extract of P. ostreatus group) received ethylene glycol in drinking tap water (0.75% v/v) ad libitum for nine weeks and was supplemented with the P. ostreatus aqueous extract by oral gavage at dose level of 100 mg (infused in 5 mL boiling distilled water)/kg b.w. daily during the last seven weeks.
Group 4 (ethylene glycol and aqueous extract ofA. bisporusgroup) was given ethylene glycol in drinking tap water (0.75% v/v) ad libitum for nine weeks and was supplemented with the A. bisporus aqueous extract by oral gavage at dose level of 100 mg (infused in 5 mL boiling distilled water)/kg b.w. daily for the last seven weeks.
Group 5 (ethylene glycol and carvedilol group) was given ethylene glycol in drinking tap water (0.75% v/v) ad libitum for nine weeks and was supplemented with the carvedilol by oral gavage at dose level of 30 mg (dissolved in 5 mL distilled water)/kg b.w. daily during the last seven weeks.
Normal control (Group 1) was regarded as a control group for Group 2, while Group 2 was regarded as a control group for Groups 3–5.

2.9. Blood and Tissue Sampling

By the end of the experiment, rats in all groups were sacrificed under diethyl ether inhalation anesthesia after overnight fasting. For each rat, blood was obtained in clotting activated gel tubes from jugular vein. Then, the urine was collected from urinary bladder after dissection. The blood was centrifuged at 3000 round per minute (rpm) for 30 min. The sera were quickly aspirated into Eppendorf tubes for analysis of serum biomarkers of kidney functions. Specific gravity of urine from each rat was detected by Medi-Test Combi 10® SGL strips obtained from Macherey-Nagel GmbH, Neumann-Neander-Str. 6-8 D52355 Duren, Germany. The obtained sera and urine samples were kept in deep freezer at −30 °C pending their use. Kidneys of each animal were excised, and then one kidney of each rat was fixed in 10% neutral buffer formalin for histopathological and immunohistochemical studies. A half gram of kidney of each animal was homogenized in 5 mL of 0.9% isotonic sterile saline (10% w/v) by Teflon homogenizer (Glas-Col, Terre Haute, IN, USA). The homogenates were centrifuged at 3000 rpm for 5 min and the homogenate supernatants were separated for determination of calcium and oxalate levels.

2.10. Biochemical Analysis

Serum and urine creatinine, urea and uric acid levels were determined by kits obtained from Diamond Diagnostics (Egypt) based on the methods of Murray [55], Tabacco et al. [56] and Fossati et al. [57], respectively. Serum, urine and kidney oxalate content were assayed based on the method of Young [58] by using kits from Ben-Biochemical Enterprise (Italy). Kidney calcium content was determined by using kits of Biodiagnostic (Egypt) based on the method of Gindler and King [59]. Fex Urea was calculated from formula: Fex Urea= [(urine urea/serum urea)/(urine creatinine/serum creatinine)] × 100 [60].

2.11. Determination of TNF-α and IL-1β Levels by ELISA

Serum TNF-α level was determined by rat TNFα ELISA kit purchased from MyBioSource, Inc., San Diego, CA 92195-3308 USA according manufacturer’s instructions. Serum IL-1β level was estimated by rat IL-1β ELISA kit purchased from Cloude-Clone Corp., Katy, TX 77494, USA according manufacturer’s instructions.

2.12. Histological Investigations

The kidneys fixed in 10% neutral buffered formalin were sent to the Department of Pathology, National Cancer Institute, Cairo University, Egypt for processing, blocking, sectioning and staining with haematoxylin and eosin based on the method of Banchroft et al. [61]. The stained sections were examined by light microscope to detect the histological changes.

2.13. Immunohistochemical Investigations

For immunhistochemical investigations, kidney sections (4 µm thick) were mounted onto positive-charged slides (Fisher Scientific, Pittsburgh, PA, USA) to detect NF-κB, p53 and Bcl-2. The NF-κB, Bcl-2 and p53 immunoreactivity were determined following Gao and Zhou [62]. Briefly, before the incubation with antibodies, endogenous peroxidase activity was quenched, and slides were washed and then incubated in a blocking solution of hydrogen peroxide 1% in methanol in darkness for 15 min. After antigen retrieval, sections were rinsed in tap water and then phosphate buffer saline. Primary rat antibody for NF-κB (Thermo Fisher Scientific, Waltham, MA 02451, USA) and rat antibodies for p53 and Bcl-2 (DakoCytomation, Carpinteria, CA, USA) diluted 1:100 in PBS, were applied for 1 h at 37 °C. Secondary biotinylated antibody diluted 1:100 in PBS was applied for a period of 30 min at 37 °C. Streptavidinbiotin or avidin-biotin peroxidase (ABC/HRP) was applied for 10 min at room temperature. Bound antibody complex was visualized by the reaction of 3, 3′-diaminobenzidine (DAB) substrate and counter stained with haematoxylin.

2.14. Imaging and Semi-Quantitative Analysis of NF-κB, p53 and Bcl-2 Expressions

The yellowish brown colored stained in percent area was detected by ImageJ software, US National Institutes of Health, Bethesda, Maryland, USA (http://imagej.nih.gov/ij/).

2.15. Western Blot Analysis

The ReadyPrepTM protein extraction kit (total protein) obtained from Bio-Rad Inc. (Catalog #163-2086) was employed according to manufacturer’s instructions. Bradford Protein Assay Kit (SK3041) for quantitative protein analysis was provided by Bio basic Inc. (Markham, Ontario, L3R 8T4, Canada) according to manufacturer’s instructions. Protein in each sample was loaded and separated by using TGX Stain-Free™ FastCast™ Acrylamide Kit (SDS-PAGE), provided by Bio-Rad Laboratories Inc. (Cat # 161-0181), according to manufacturer’s instructions. The protein bands separated by polyacrylamide gel electrophoresis were transferred from gel to PDVF (polyvinylidene difluoride) membrane using BioRad Trans-Blot Turbo. Tris-buffered saline with Tween 20 (TBST) buffer and 3% bovine serum albumin (BSA) was used to block the membrane at room temperature for 1 h. The 1ry antibodies NF-κB p65, NF-κB and Bax purchased from Santa Cruz Biotechnology, Inc. (USA) as well as Bak purchased from Aviva Systems Biology (7700 Ronson Road, Ste 100, San Diego, CA 92111 USA) were diluted in TBST according to manufactured instructions. Incubation was done overnight for each 1ry antibody solution, against the blotted target protein, at 4 °C. The blot was rinsed 3–5 times for 5 min with TBST. Incubation was done for the horse raddish peroxidase (HRP)-conjugated 2ry antibody (Goat anti-rabbit IgG – HRP – 1 mg Goat MAb; Novus Biologicals) solution against the blotted target protein for 1 h at room temperature. Then, the blot was rinsed 3–5 times for 5 min with TBST. The chemiluminescent substrate (ClarityTM Western ECL substrate Bio-Rad cat#170-5060) was applied to the blot based on the manufacturer’s recommendation. Briefly, equal volumes were added from both solution A (Clarity Western luminal/enhancer solution) and solution B (peroxidase solution). The chemiluminescent signals were captured using a CCD (charge coupled device) camera-based imager. Image analysis software was used to read the band intensity of the target proteins against control sample β-actin (housekeeping protein) by protein normalization on the ChemiDoc MP imager.

2.16. Statistical Analysis

The data were analyzed using the one-way analysis of variance (ANOVA) by PC-STAT program [63] followed by LSD test to compare different groups with each other. Data were expressed as mean ± standard error means (SEM). F-probability obtained from one-way ANOVA expresses the general effect on each parameter between groups throughout the experiment.

3. Results

3.1. Phytochemical Screening

Phytochemical analysis (Table 1) of P. ostreatus and A. bisporus indicated the presence of carbohydrates (or glycosides), alkaloids, flavonoids, resins, tannins and unsaturated sterols.

3.2. GC-MS Analysis of P. ostreatus Aqueous Extract

The GC-MS analysis of P. ostreatus aqueous extract (Table 2, Figure 2 and Figure S2) indicated the identification of nineteen phytochemicals. The most abundant constituents were N-hydroxy-N-methyl methenamine (24.2%) and (S)-(+)-isoleucinol (23.0%).

3.3. GC-MS Analysis of A. bisporus Aqueous Extract

The GC-MS analysis of A. bisporus aqueous extract (Table 3, Figure 3 and Figure S3) allowed the identification of fourteen different phytochemicals. The most abundant constituents include N-methoxy-methanamine (30.6%), 6-ethyl-2,3-dihydro-2,7-dimethyl-5-oxo-5H-oxazolo[3,2-a]pyridine-8-carbonitrile (13.7%) and Fumaric acid, 2-heptyl octyl ester (13.11%).

3.4. Effect on Body Weight, Kidney Weight and Relative Kidney Weight

Administration of ethylene glycol to Wistar rats induced a highly significant decrease (p < 0.01; LSD) in body weight, by 15.29%, as compared with normal control. The treatment of ethylene glycol-induced hyperoxaluric rats with A. bisporus infusion and carvedilol induced a significant increase (p < 0.05; LSD) while the treatment with P. ostreatus infusion produced a non-significant increase (p > 0.05; LSD). On the other hand, the kidney weight and relative kidney weight significantly increased (p < 0.01; LSD) in ethylene glycol-induced hyperoxaluric rats recording changes of 46.92% and 93.91%, respectively, as compared with the normal control. Meanwhile, the treatment of hyperoxaluric rats with mushroom infusions and carvedilol has no significant effect (p > 0.05; LSD) on kidney weight and relative kidney weight as compared with the ethylene glycol-induced hyperxaluric Wistar rats (Figure 4 and Figure S4).

3.5. Effect on Serum Creatinine, Urea and Uric Acid Levels

Administration of ethylene glycol to Wistar rats induced a highly significant increase (p < 0.01; LSD) in serum creatinine, urea and uric acid levels by 53.52%, 159.97% and 95.05%, respectively, as compared with normal control. The treatment of ethylene glycol-induced hyperoxaluric rats with P. ostreatus and A. bisporus infusions, meanwhile, induced a highly significant decrease (p < 0.01; LSD) in creatinine and urea levels. The uric acid level was non-significantly (p > 0.05; −17.26%) and significantly (p < 0.05; −26.90%) decreased as a result of treatment with P. ostreatus and A. bisporus, respectively, while treatment with carvedilol caused a non-significant (p > 0.05; LSD) decrease of all above parameters (Figure 5 and Figure S5). Thus, A. bisporus extract followed by P. ostreatus extract seemed to be more effective in reducing elevated serum creatinine, urea and uric acid levels in hyperoxaluric rats.

3.6. Effect on Urine Creatinine, Urea and Uric Acid Levels

After administration of ethylene glycol to albino rats, urine creatinine and urea levels reduced very significantly (p < 0.01; LSD) while, urine uric acid level was non-significantly affected (p > 0.05; LSD) compared to the normal control. Treatment with P. ostreatus and A. bisporus, however, led to a highly significant increase (p < 0.01; LSD) of urine creatinine level, while urine urea was non-significantly (p > 0.05; 40.08%) and significantly (p < 0.05; 53.18%) increased as a result of treatment with P. ostreatus and A. bisporus, respectively. On the other hand, urine uric acid level decreased non-significantly (p > 0.05; −15.49%) with P. ostreatus and highly significant (p < 0.01; −34.41%) with A. bisporus. In contrast, treatment with carvedilol resulted in only non-significant alterations (p > 0.05; LSD) in all of the above parameters compared with ethylene glycol control rats (Figure 6 and Figure S6). Overall, therefore, A. bisporus followed by P. ostreatus appeared to be more effective in increasing the urine creatinine and urea levels and decreasing urine uric acid levels than carvedilol.

3.7. Effect on Various Ratios Related to Kidney Functions:

The effects on various ratios related to kidney functions are depicted in Figure 7 and Figure S7. Highly significant reductions (p < 0.01; LSD) in urine creatinine/serum creatinine, urine urea/ serum urea and Fex Urea ratios were induced as a result of administering ethylene glycol to albino rats recording changes of −50.59%, −82.41% and −64.55%, respectively, as compared to the normal control.
The treatment of ethylene glycol-induced urolithic rats with all the tested agents, on the other hand, led to highly significant increases (p < 0.01; LSD) in the urine creatinine/serum creatinine ratio. With respect to the urine urea/serum urea ratio, significant (p < 0.05; 80.17%), highly significant (p < 0.01; 211.66%) and non-significant (p > 0.05; 33.77%) increases were attained following the treatment with P. ostreatus, A. bisporus and carvedilol, respectively. Fex Urea was non-significantly increased (p > 0.05; LSD) after treatment with P. ostreatus and carvedilol and significantly increased (p < 0.05; 37.69%) after treatment with A. bisporus.

3.8. Effect on Serum, Urine and kidney Oxalate Levels

Serum, urine and kidney oxalate levels were highly significantly increased (p < 0.01; LSD) as a result of administration of ethylene glycol to albino rats recording changes of 81.39%, 5446.93% and 155.75%, respectively, as compared to the normal control. The treatment of ethylene glycol-induced urolithic rats with P. ostreatus, A. bisporus and carvedilol, however, induced a decline in the serum oxalate level, which was significant with P. ostreatus and highly significant with A. bisporus and carvedilol. On the other hand, a highly significant (p < 0.01; LSD) decrease in urine and kidney oxalate levels was produced as a result of treatment with the mushroom infusions and carvedilol (Figure 8 and Figure S8). Overall, A. bisporus extract was the most effective in decreasing kidney oxalate level while carvedilol was the most effective in decreasing urine oxalate.

3.9. Effect on Urine Specific Gravity

The urine specific gravity exhibited similar behavioral pattern as urine oxalate level. The ethylene glycol-induced hyperoxaluric rats exhibited a significant increase (p < 0.01; LSD) in urine specific gravity as compared to normal control group. The treatment of ethylene glycol-induced with P. ostreatus and A. bisporus aqueous extracts and carvedilol produced a significant decrease (p < 0.01; LSD) of the elevated urine hyperoxaluric rats with specific gravity (Figure 9 and Figure S9). P. ostreatus aqueous extract and carvedilol was more effective than A. bisporus aqueous extract in decreasing the elevated urine specific gravity.

3.10. Effect on Kidney Calcium Level

Administration of ethylene glycol induced a significant increase (p < 0.05; 36.45%) in kidney calcium level compared to the normal control. Kidney calcium levels were significantly decreased as a result of treatment with A. bisporus (p < 0.05; −25.98%) and non-significantly decreased following treatment with P. ostreatus (p > 0.05; −2.94%) and carvedilol (p > 0.05; −17.28%) as compared with the urolithic control group (Figure 10 and Figure S10). Thus, A. bisporus infusion seemed to be the most potent in decreasing the elevated kidney calcium and oxalate content in ethylene glycol-induced hyperoxaluric rats.

3.11. Effects on Serum TNF-α and IL-1β Levels

The ethylene glycol-induced hyperoxaluric rats exhibited a highly significant elevation (p < 0.01; LSD) in serum TNF-α and IL-1β levels, with changes of 437.25% and 285.75% respectively, as compared with normal control. The treatment of the ethylene glycol-induced hyperoxaluric rats with P. ostreatus and A. bisporus aqueous extracts and carvedilol induced a highly significant decrease (p < 0.01; LSD) of the elevated serum TNF-α and IL-1β levels; carvedilol was the most potent (Figure 11 and Figure S11).

3.12. Histological Effects

Microscopical examination of kidney sections of normal rats (Figure 12a–c and Figure S12) revealed the tissue to have a normal histological structure. The kidney is divided into an inner region, the medulla and an outer region, the cortex. The medulla consists of collecting tubules and thin segments comprising the loop of Henle. The cortex, meanwhile, contains glomeruli and tubules.
In rats administered with ethylene glycol, atrophy and congestion were observed in the glomerular tufts, and the lumina of the renal tubules were affected by protein casts (Figure 13a and Figure S13), cellular casts, interstitial nephritis, glomerular hemorrhages (Figure 13b), necrosis and dense oxalate crystals (Figure 13c). In addition, as shown in Figure 13d, the kidney tissues exhibited dysplastic tubular cells and focal necrosis associated with massive infiltration of inflammatory cells within the renal tubules, as well as enlarged vesicular nuclei with an irregular arrangement (dysplasia and anaplasia) in the lining of the epithelium of some renal tubules (Figure 13e), and infiltration of focal inflammatory cells, necrosis, cystic dilatation and apoptotic cells (AP) in other renal tubules (Figure 13f).
As shown in Figure 14 and Figure S14, once ethylene glycol-administered rats were treated with P. ostreatus, homogenous eosinophilic casts were evident in the lumina of a few medullary tubules (Figure 14a). Moreover, slight congestion was observed in intertubular renal blood capillaries (Figure 14b,c) and in the glomerular tufts (Figure 14d). The congestion observed in the cortical blood vessels and the glomeruli was associated with oedema and infiltration of inflammatory cells into the perivascular tissue (Figure 14e). Despite these histological changes, the kidney architecture was markedly improved compared to that of ethylene glycol-administered control rats.
Figure 15 and Figure S15 show the histological results of treatment of ethylene glycol-administered rats with A. bisporus, revealing a considerable improvement in the kidney architecture. In that context, Figure 15a shows presence of red blood cells in and between the tubules at the medulla, while Figure 15b displays normal renal parenchyma with slight glomerular congestion. Figure 15c illustrates some congestion of renal blood vessels and glomeruli and Figure 15d shows the presence of small protein casts in the lumina of some renal tubules associated with mild congestion in the glomeruli.
Figure 16 and Figure S16 shows the histological results of treatment of ethylene glycol-administered rats with carvedilol. Here, Figure 16a manifests the presence of red blood cells in the lumina of some medullary tubules, while Figure 16b reveals slight congestion in the cortical blood vessels and glomeruli. Figure 16c shows vacuolization of the epithelium lining the tubules while Figure 16d demonstrates, in addition to the latter change, hypertrophy and vacuolization of the glomerular tufts associated with infiltration of inflammatory cells into the perivascular tissue. Overall, the group treated with carvedilol showed noticeable amelioration of many the histological changes originally apparent after the administration of ethylene glycol.

3.13. Effect on Immunohistochemically Detected Kidney NF-κB, p53 and Bcl-2

In the present study, immunohistochemical staining was used to detect the expression of NF-κB, p53 and Bcl-2 in kidney tissues of the albino rats. NF-κB expression in cytoplasm and nuclei (illustrated by a yellowish brown colored staining) was noticeably increased in the kidneys of ethylene glycol control rats (Figure 17b and Figure S17) compared to normal rats (Figure 17a). The treatment of ethylene glycol-induced hyperoxaluric rats with extracts of P. ostreatus and A. bisporus and with carvedilol decreased the expression of NF-κB (Figure 17c–e); P. ostreatus and A. bisporus extracts were more effective than carvedilol. Similarly, p53 protein concentration (yellowish brown color) was remarkably increased in the cytoplasm and nuclei of the ethylene glycol control group (Figure 18b and Figure S18) as compared with normal rats (Figure 18a). Again, however, P. ostreatus, A. bisporus and carvedilol treatments all markedly reduced the p53 expression; P. ostreatus extract and carvedilol were more effective than A. bisporus extract (Figure 18–e). With respect to the expression of Bcl-2 (yellowish brown color) in the cytoplasm of the ethylene glycol rats, Figure 19b indicates a decrease as compared with normal rats (Figure 19a and Figure S19). Treatment of the ethylene glycol-induced urolithic rats with P. ostreatus and A. bisporus extracts and carvedilol appeared to lead to a considerable increase in the expression of Bcl-2; P. ostreatus and A. bisporus extracts were more effective than carvedilol (Figure 19c–e).
With respect to statistical analysis of ImageJ results of immunohistochemical stained sections, ethylene glycol administration was found to be associated with highly significant increases in the expressions of NF-κB (p < 0.01; 103.55%) and a significant (p < 0.05; 16.08%) increase in p53 in the kidney compared to the normal control while the expression of Bcl-2 reduced highly significantly (p > 0.05; −92.42%). When the ethylene glycol-administered rats were supplemented with mushroom extracts, there was a highly significant (p < 0.01; LSD) decrease in the expression of NF-κB but only a significant (p < 0.05; LSD) decrease in NF-κB expression following treatment with carvedilol. When ethylene glycol-administered rats were treated with P. ostreatus, the expression of p53 was highly significantly reduced by 17.87% (p < 0.01; LSD) while treatment with carvedilol led to a highly significant reduction of 27.65%. Treatment with A. bisporus, however, led to a non-significant (p > 0.05) reduction of 11.44% in p53 expression. All treatment agents, however, were associated with a highly significant increase (p < 0.01; LSD) in Bcl-2 expression when they were administered to rats previously treated with ethylene glycol (compared to the urolithic control group) (Figure 20 and Figure S20).

3.14. Effect on Kidney p65, p50, Bax and Bak Detected by Western Blot

The kidney NF-κB p65 and NF-κB p50 significantly increased (p < 0.01; LSD) in ethylene glycol-induced hyperoxaluric rats, by 190.48% and 153.04%, respectively, as compared with normal control. Meanwhile, the treatment of hyperoxaluric rats with P. ostreatus and A. bisporus aqueous extracts and carvedilol successfully counteracted the ethylene glycol-induced elevations in NF-κB p65 and NF-κB p50, producing a highly significant decrease (p < 0.01; LSD) as compared with the ethylene glycol-induced hyperoxaluric control rats. The effect of carvedilol was most potent in decreasing the elevated NF-κB p50 level (Figure 21 and Figure 22, Figures S21 and S22).
On the other hand, the apoptotic mediators Bax and Bak of Bcl-2 family showed a significant increase (p < 0.01; LSD) in ethylene glycol-induced hyperoxaluric rats recording increases of 241.61% and 259.79%, respectively, as compared with normal control. The treatment of hyperoxaluric rats with P. ostreatus and A. bisporus aqueous extracts and carvedilol successfully resulted in a significant decrease (p < 0.01; LSD) in the elevated NF-κB p65 and NF-κB p50 expression as compared with the ethylene glycol-induced hyperoxaluric control rats. Carvedilol was the most potent in decreasing the elevated Bax and Bak levels (Figure 23 and Figure 24, Figures S23 and S24).

4. Discussion

The two tested mushrooms P. ostreatus and A. bisporus were subjected to preliminary phytochemical screening and GC-MS analysis of their aqueous extracts. The phytochemical screening indicated the presence of glycosides, alkaloids, flavonoids, resins, tannins and unsaturated sterols. Most of these compounds were proven, by many publications, to have biological activities, e.g., antimicrobial, anti-inflammatory and antioxidant [64,65,66]. Moreover, many of the major compounds and chemical groups, detected in P. ostreatus aqueous extract by GC-MS, have been reported to have antioxidant and anti-inflammatory properties; these include (S)-(+)-isoleucinol [67], N-hydroxy-N-methyl-methanamine [66], phenylethanal [68,69] and 2-pyrrolidinone [70,71]. On the other hand, GC-MS of A. bisporus extract revealed the presence of multiple antioxidant and anti-inflammatory abundant constituents and chemical groups including N-methoxy-methanamine, [66], 2-pyrrolidinone [70,71] and fumaric acid, 2-heptyl octyl ester [72,73,74,75].
In the present study, the body weight significantly decreased in the ethylene glycol-supplemented control rats and the administration of aqueous extracts of P. ostreatus and A. bisporus as well as carvedilol to ethylene glycol-administered rats resulted in a remarkable increase in body weight. It is worth mentioning that the body weight loss is considered as a good reliable sensitive toxicity indicator [76,77,78]. Thus, the decrease in body weight, in the present study, by ethylene glycol may represent the first preliminary indicator of its toxicity. The prevention of decrease in body weight in ethylene glycol-administered rats by P. ostreatus and A. bisporus aqueous extracts and carvedilol may be due to their ability to antagonize the toxicity effects of ethylene glycol. The amendment of the biochemical and histological perturbations by the mushroom extracts and carvedilol, in the present study, may lead to improvement of general health and feeding ability. On the other hand, kidney weight and relative kidney weight in the ethylene glycol-administered rats exhibited a significant increase as compared with the normal control. That increase may be due to inflammation, fluid accumulation and crystal formation in the kidney as a result of ethylene glycol administration [28,79,80]. These results are in concordance with Wang et al. [81], Saeidi et al. [82] and Aggarwal et al. [83] publications, which demonstrated that the body weight was significantly reduced both in hyperoxaluric and lithogenic rats as compared with normal control rats while kidney weight and relative kidney weight showed a significant increase. In contrast, Noorafshan et al. [84] found that kidney weight and relative kidney weight decreased in ethylene glycol-administered control rats as compared with normal control rats. The treatment of ethylene glycol-induced hyperoxaluric rats with P. ostreatus and A. bisporus aqueous extracts and carvedilol, in the current study, did not significantly alter the kidney weight and relative kidney weight as compared with ethylene glycol-administered control.
In the present experiments, the administration of ethylene glycol led to a rise in serum creatinine, serum urea, serum uric acid and urine uric acid concentrations, as well as a decrease in urine creatinine, urine urea levels and ratios of urine creatinine/serum creatinine, urine urea/serum urea and Fex Urea. The decline in urine creatinine/serum creatinine, urine urea/serum urea and Fex urea ratios may be attributed to the diminution in creatinine, urea and uric acid clearance from blood to urine due to reduction in the glomerular filtration rate in addition to the damage in the renal tubular cells [85,86,87]. The results are in agreement with many investigators [13,88,89,90]. As to how these effects are caused, it was stated that drugs inducing nephrotoxicity are often associated with remarkable increases in acute tubular necrosis and blood urea [91]. In this regard, it has been shown that severe damage in proximal tubule cells may cause increases in serum creatinine and urea [87]. This damage appears to inhibit clearance of waste products, particularly nitrogenous substances such as blood creatinine, urea and uric acid, meaning that they accumulate in the blood [92,93,94]. The deteriorations in the biomarkers of kidney function and glomerular filtration rate as well clearance of waste by-products were concomitant with atrophy and congestion of glomeruli as well as necrosis and apoptosis of renal tubular cells as indicated in the present histological studies.
High levels of urine uric acid (evident in the present research, in the ethylene glycol control group) point to an increased risk of stone formation since urine uric acid is considered one of the most important promoters of crystallization [93]. This postulation aligns with the publication, which revealed that hyperuricosuria can be considered the main risk factor for the formation of urinary uric acid stones and may also play a role in CaOx lithiasis [95]. The predominance of uric acid crystals in CaOx stones and the observation that uric acid binding proteins are able to binding to CaOx to modify its crystallization reflect its essential role in the formation of stones [5,96,97].
The contribution of the present study is to show that seven weeks of treatment with aqueous extracts of P. ostreatus and A. bisporus, like treatment with carvedilol, reduced the elevation in serum creatinine, serum urea, serum uric acid and urine uric acid; P. ostreatus and A. bisporus seemed to be more potent than carvedilol. The treatments also produced an increase in the levels of urine creatinine, urine urea and ratios urine creatinine/serum creatinine and urine urea/serum urea as well as Fex Urea; P. ostreatus and A. bisporus appeared to be more effective. These changes may be attributed to the increased clearance of blood creatinine, urea and uric acid into urine. These treatment outcomes are consistent with other publications in different models of kidney injuries [86,98,99,100,101]. In our opinion, the improvements in serum and urine parameters and ratios related to kidney function as a result of treatments of hyperoxalouric rats with mushroom extracts and carvedilol may be secondary to their preventive effects against ethylene glycol-induced deteriorations in kidney histological architecture and integrity. The histological evidences, in the current study, support this elucidation since the treatments with mushroom extracts and carvedilol produced marked amelioration in kidney histological lesions produced by ethylene glycol supplementation.
Ethylene glycol administration, in the current study, caused a significant elevation in levels of calcium in the kidneys and in levels of oxalate in serum, urine and kidney. These findings parallel those of several researchers [13,102,103,104,105]. In addition, it was also elucidated by other investigators that the formation of stones in ethylene glycol-administered animals is caused by hyperoxaluria, which leads to elevation of both kidney excretion and retention of oxalate [106]. It is known from previous publications that an imbalance between the promoters of lithogenesis such as phosphate, oxalate, calcium, uric acid and low urine volume on the one hand and inhibitors including magnesium, citrate and macromolecules, on the other hand may represent a critical condition for urolithiasis [103,107]. Thus, the elevation of kidney oxalate and kidney calcium in association with the increase in uric acid, in the present study, activates the process of crystallization and precipitation of crystalline material as CaOx. In that manner, other past publications showed that the crystals of CaOx and high oxalate concentrations in nephrons damages epithelial cells, inducing nucleation of heterogeneous crystal and causing crystals aggregation [108,109]. In support to this evidence, the histological findings of the present study depicted the presence of oxalate crystals in the lumen of the renal tubules in association with inflammation and necrosis of renal tubules.
Treatment of ethylene glycol-administered rats with the tested mushroom extracts and carvedilol reduced the above risk factors. Thus, P. ostreatus, A. bisporus and carvedilol treatments led to reduced levels of serum and urine oxalate, which was associated with a decrease in the level of crystal components (calcium and oxalate) in kidney homogenate. These results are consistent with the present histological investigations, which depicted the absence of oxalate crystals in the renal tubules in ethylene glycol-induced urolithic rats treated with P. ostreatus, A. bisporus and carvedilol.
In association with the significant increase in urine uric acid and oxalate levels in the ethylene glycol-administered rats in the present study, the urine specific gravity significantly elevated in comparison with normal control. These results are in concordance with Kandhare et al. [110] and in discordance with Cruzan et al. [111]. The increase in urine specific gravity and urine uric acid and oxalate content in ethylene glycol-administered rats are important indices for the increased possibility for the formation of urinary calculi. On the other hand, the treatments of the ethylene glycol-administered rats with P. ostreatus and A. bisporus aqueous extracts and carvedilol produced a significant decrease in the specific gravity of urine towards the normal values. In our opinion, this decrease in specific gravity may be due to the resultant decrease in urine levels of uric acid and oxalate.
In the current study, administration of ethylene glycol, which leads to hyperoxaluria and nephrotoxicity, was evidenced by histopathological investigations, which showed the presence of marked atrophy in the glomerular tufts, protein and cellular casts, interstitial nephritis and many oxalate crystal precipitations in the lumina of the renal tubules. These results are in concordance with those of other authors who found tubular hypertrophy, interstitial inflammation, tubulointerstitial damage and extensive deposition of CaOx crystals in the renal tubules of different urolithiatic rat models [112,113,114,115,116]. In the present study, as a result of ethylene glycol administration, renal tubules exhibited cystic dilatation, focal necrosis associated with massive inflammatory cells infiltration, presence of dysplasia and anaplasia in the lining epithelium of some renal tubules, and infiltration of focal inflammatory cells and apoptotic cells in other renal tubules. These changes agree with the results obtained by Li et al. who observed severe dilatation of kidney tubules and massive inflammatory cell infiltration in ethylene glycol-administered rats [117]. Furthermore, Bashir and Gilani postulated that the dilatation of the renal tubules may be due to the obstruction in the distal renal tubular flow by large crystals [118]. In rats exposed to low levels of ethylene glycol, the renal damage (a proximal tubule cell necrosis) is directly related to the amount of accumulation of calcium oxalate in kidney tissue [111,119]. The necrotic damage is most likely due to the accumulation of calcium oxalate crystals, since, of the various ethylene glycol metabolites, only oxalate is cytotoxic to kidney cells in culture at relevant concentrations [120,121].
The inflammation observed in the histopathological observations in kidney of ethylene glycol-induced hyperoxaluric rats, in the present study, was confirmed by a significant increase in the levels of serum TNF-α and IL-1β as well as an increase in the kidney NF-κB, NF-κB p65 and NF-κB p50. The treatments of hyperoxaluric rats with P. ostreatus and A. bisporus aqueous extracts and carvedilol produced a significant decrease in these inflammatory mediators. Thus, the three treatments have potent anti-inflammatory potentials. It is relevant here to mention that TNF-α and IL-1β are T helper 1 (Th1) cytokines and are important stimuli for activation of NF-κB that is found in almost animal cell types including renal cells [122,123]. In an inactivated state, NF-κB in the cytosol is presented complexed with the inhibitory protein IκBα [124]. A variety of extracellular signals including TNF-α and IL-1β (canonical pathway) can activate the enzyme IκB kinase (IKK), which results in dissociation of NF-κB from IκBα and subsequent proteasomal degradation of IκBα [124,125]. This allows the release of the p65/p50 heterodimers and their translocation into the nucleus, where they can bind to their specific sequences of DNA and promote NF-κB target genes involved in inflammatory, immune and acute phase responses (Figure 25) [126,127,128]. Thus, based on the present results and previous literatures, it can be suggested that P. ostreatus and A. bisporus aqueous extracts and carvedilol may produce their anti-inflammatory effects by affecting the canonical pathway of NF-κB activation (Figure 25 and Figure S25).
Increased apoptosis evidenced, in the present study, by histopathological examination of kidney of ethylene glycol-induced hyperoxaluric rats, was supported by immunohistochemical and Western blot investigations, which revealed a remarkable increase in pro-apoptotic proteins p53, Bax and Bak as well as a decrease in the anti-apoptotic mediator, Bcl-2. The treatments of hyperoxaluric rats with P. ostreatus and A. bisporus aqueous extracts and carvedilol produced a significant decrease in such elevated pro-apoptotic proteins and increase in the lowered anti-apoptotic mediator Bcl-2 in the kidney. It is worth mentioning that p53, Bax and Bak as well as Bcl-2 are implicated in the intrinsic pathway of apoptosis that is activated by ROS produced by mitochondria (Figure 25 and Figure S25). The tumor suppressor p53 is a transcription factor that is activated upon DNA damage to induce target genes involved in either cell growth arrest or apoptosis [129,130,131]. The p53, Bax and Bak mediate intrinsic signaling pathway to activate caspase-9 that in turn activate caspase-3 leading to apoptosis (Figure 25 and Figure S25) [132]. This activation can be controlled by the Bcl-2, which has anti-apoptotic effects [130,131,132,133]. Otherwise, TNF-α activates the extrinsic pathway of apoptosis by its binding to TNF receptor (TNFR) and death receptor (Figure 25 and Figure S25). In addition, NF-κB was reported to have a role in the extrinsic pathway of apoptosis. NF-κB can oppose or promote apoptosis depending on the specific cell type and the type of inducer [134]. Although many publications reported the anti-apoptotic roles of NF-κB, many others revealed its pro-apoptotic and apoptotic actions in other circumstances [135,136,137,138,139]. Based on the findings of the present study and previous publications, it can be elucidated that P. ostreatus and A. bisporus aqueous extracts and carvedilol may produce their inhibitory effects on apoptosis by affecting both extrinsic and intrinsic pathways (Figure 25 and Figure S25).
Stone formation is related with the sedimentation of fragments in the peritubular field and in the medullary interstitium, and such sedimentation can create inflammation and aid the advancement of fibrosis, which follows tubular cell damage and is a determinant of kidney function [140]. In addition, ROS led to a robust inflammatory response in the kidneys of rats with hyperoxaluria and CaOx nephrolithiasis [5,28,141]. In this regard, it was suggested that renal tubular crystal deposition and apoptotic changes induced by hyperoxaluria play a role in the pathogenesis of urolithiasis [5,142]. In addition, it was speculated that renal tubular epithelial cell injury, apoptosis and inflammation are involved in melamine-related kidney stone formation [143]. Cell apoptosis and proliferation in the kidney cortex and medulla were enhanced in response to the glyoxylate-induced CaOx crystal formation and deposition [144]. In turn, apoptosis of renal tubular cells may promote stone formation via cellular demise and post-apoptotic necrosis, which could stimulate calcium oxalate crystal aggregation and growth as, indicated in Figure 25 and Figure S25 [5]. This postulation has been supported by in vitro study on Madin-Darby Canine Kidney (MDCK) cells which were exposed to oxalate ions [145]. Based on the previous findings and literature, it can be suggested that augmentation of inflammation and apoptosis in hyperoxaluric rats (Figure 25 and Figure S25) may have an important role in oxalate crystal formation and growth. Thus, the suppression of inflammation and apoptosis by treatment of hyperoxaluric rats with P. ostreatus and A. bisporus extracts and carvedilol may be implicated to reduce oxalate crystal formation and growth.
The treatment of ethylene glycol-administered rats with P. ostreatus and A. bisporus extracts and carvedilol led to decrease in renal expression of NF-κB, NF-κB p65, NF-κB p50, p53, Bax and Bak and increase in renal expression of Bcl-2, and it simultaneously prevented the ethylene glycol-induced histological deteriorations, inflammations and apoptosis in kidney. P. ostreatus and A. bisporus extracts were more effective on NF-κB and Bcl-2 than carvedilol while carvedilol was the most potent in decreasing the elevated kidney p53, NF-κB p50, Bax an Bak. These results are in accordance with those of many authors. Jedinak et al. concluded that P. ostreatus possesses anti-inflammatory activities and could be considered a dietary agent against inflammation [146]. Also, Amstad et al. elucidated that Bcl-2-overexpressing cells have an elevated expression of antioxidant enzymes and have higher levels of cellular GSH [147]. Besides, Volman et al. noticed that NF-κB transactivation in human intestinal Caco-2 cells was lowered by polysaccharide extract of A. bisporus [148]. Meanwhile, other investigators reported that the vasodilatory β-blocker carvedilol exhibits additional effects in ameliorating inflammation [149,150,151]. In another way, it was found that the pre-treatment of potassium dichromate-induced nephrotoxicity in rats with carvedilol caused a decrease in p53 and an increase in Bcl-2 expression [152].
In our previous study, we found that the treatment of ethylene glycol-administered rats with P. ostreatus and A. bisporus extracts and carvedilol produced potent inhibitory effects on kidney oxidative stress represented by decrease in lipid peroxidation and nitric oxide and potent enhancement in the kidney antioxidant defense system marked by increase in glutathione content and glutathione-S-transferase, glutathione peroxidase, superoxide dismutase and catalase activities [28]. This led us to suggest that the ameliorative effects on kidney function and histological integrity as well as anti-apoptotic and anti-inflammatory effects P. ostreatus, A. bisporus and carvedilol may be mediated, at least in part, via suppression of the oxidative stress and enhancement of antioxidant defense system (Figure 25 and Figure S25).
In conclusion, the present study demonstrated that P. ostreatus and A. bisporus aqueous extracts and carvedilol protected against ethylene glycol-induced rat kidney dysfunction, histological perturbances, oxalate crystal formation, inflammation and apoptosis. P. ostreatus and A. bisporus aqueous extracts were more potent than carvedilol in many instances. In spite of these potential effects, further clinical studies are required to estimate the safety and efficacy of P. ostreatus and A. bisporus extracts in human beings.

Supplementary Materials

The following are available online at https://www.mdpi.com/2218-273X/10/9/1317/s1, Figure S1: P. ostreatus (A) and A. bisporus (B); Figure S2: GC-MS analysis of P. ostreatus aqueous extract; Figure S3: GC-MS analysis of A. bisporus aqueous extract; Figure S4: Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on body weight, kidney weight and relative kidney weight of ethylene glycol-administered rats.; Figure S5: Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on levels of serum parameters related to kidney function of ethylene glycol-administered rats; Figure S6: Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on different urine parameters related to renal efficiency of ethylene glycol-administered rats; Figure S7: Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on various ratios related to kidney function of ethylene glycol-administered rats; Figure S8: Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on serum, kidney and urine oxalate levels in ethylene glycol-administered rats; Figure S9: Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on urine specific gravity in ethylene glycol-administered rats; Figure S10: Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on kidney calcium content in ethylene glycol-administered rats; Figure S11: Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on serum TNF-α and IL-1β levels in ethylene glycol-administered rats; Figure S12: Photomicrographs of hematoxylin and eosin stained sections of kidney of a normal control rat; Figure S13: Photomicrographs of hematoxylin and eosin stained sections of kidney of ethylene glycol control rat; Figure S14: Photomicrographs of hematoxylin and eosin stained sections of kidney of ethylene glycol-administered rat treated with P. ostreatus aqueous extract; Figure S15: Photomicrographs of hematoxylin and eosin stained sections of kidney of ethylene glycol-administered rat treated with A. bisporus aqueous extract; Figure S16: Photomicrographs of hematoxylin and eosin stained sections of kidney of ethylene glycol-administered rat treated with carvedilol; Figure S17: Photomicrographs (a–e) of immunohistochemically stained kidney sections for detection of NF-κB in different groups; Figure S18: Photomicrographs (a–e) of immunohistochemically stained kidney sections for detection of p53; Figure S19: Photomicrographs of immunohistochemically stained kidney sections for detection of Bcl-2; Figure S20: Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on percent area of yellowish brown color of NF-κB, p53 and Bcl-2 expressions; Figure S21: Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on relative kidney NF-κB p65 expression detected by Western blot in ethylene glycol-administered rats; Figure S22: Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on relative kidney NF-κB p50 expression detected by Western blot in ethylene glycol-administered rats; Figure S23: Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on relative kidney Bax expression detected by Western blot in ethylene glycol-administered rats; Figure S24: Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on relative kidney Bak expression detected by Western blot in ethylene glycol-administered rats; Figure S25: Schematic diagram showing the effects of P. ostreatus and A. bisporus extracts and carvedilol on NF-κB, p53 and Bcl-2 to suppress inflammation and apoptosis together with the effects on oxidative stress.

Author Contributions

Conceptualization, O.M.A. and H.E.; supervision, O.M.A. and H.E.; methodology, M.R.; validation, O.M.A., E.-S.E.-N., M.R. and I.M.A.; visualization, O.M.A., H.E., M.R. and I.M.A.; biochemical investigation, O.M.A. and M.R.; histological and immunohistochemical investigation, H.E., E.-S.E.-N. and M.R.; statistical analysis, O.M.A. and M.R.; writing—original draft preparation, O.M.A., H.E. and M.R.; and writing—review, editing and final revision, O.M.A, H.E., E.-S.E.-N. and I.M.A. All authors have read and agreed to the published version of the manuscript.

Funding

This research and the APC was funded by Deanship of Scientific Research at King Saud University for funding the work through research group Project no. RG-1436-004.

Acknowledgments

The authors also acknowledge the Deanship of Scientific Research at King Saud University for funding the work through research group Project No. RG-1436-004.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Ilhan, M.; Ergene, B.; Süntar, I.; Özbilgin, S.; Çitoğlu, G.S.; Demirel, M.A.; Keleş, H.; Altun, L.; Akkol, E.K. Preclinical evaluation of antiurolithiatic activity of Viburnum opulus L. on sodium oxalate-induced urolithiasis rat model. Evid. Based Complement Altern. Med. 2014, 2014, 578103. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  2. Rad, A.K.; Hajzadeh, M.; Rajaei, Z.; Sadeghian, M.; Hashemi, N.; Keshavarzi, Z. Preventive effect of Cynodon dactylon against ethylene glycol-induced nephrolithiasis in male rats. Avicenna J. Phytomed. 2011, 1, 14–23. [Google Scholar]
  3. Laikangbam, R.; Damayanti Devi, M. Inhibition of calcium oxalate crystal deposition on kidneys of urolithiatic rats by Hibiscus sabdariffa L. extract. Urol. Res. 2012, 40, 211–218. [Google Scholar] [CrossRef] [PubMed]
  4. Atmani, F.; Slimani, Y.; Mimouni, M.; Aziz, M.; Hacht, B.; Ziyyat, A. Effect of aqueous extract from Herniaria hirsuta L. on experimentally nephrolithiasic rats. J. Ethnopharmacol. 2004, 95, 87–93. [Google Scholar] [CrossRef]
  5. Alelign, T.; Petros, B. Kidney stone disease: An update on current concepts. Adv. Urol. 2018, 2018, 3068365. [Google Scholar] [CrossRef]
  6. Peck, A.B.; Canales, B.K.; Nguyen, C.Q. Oxalate-degrading microorganisms or oxalate-degrading enzymes: Which is the future therapy for enzymatic dissolution of calcium-oxalate uroliths in recurrent stone disease? Urolithiasis 2016, 44, 45–50. [Google Scholar] [CrossRef]
  7. Danpure, C.J. Primary hyperoxaluria. In The Metabolic and Molecular Bases of Inherited Disease, 8th ed.; Scriver, C.R., Beaudet, A.L., Sly, W.S., Valle, D., Childs, B., Kinzler, K.W., Vogelstein, B., Eds.; McGraw-Hill: New York, NY, USA, 2001; Volume 2, pp. 3323–3367. [Google Scholar]
  8. Hoppe, B. An update on primary hyperoxaluria. Nat. Rev. Nephrol. 2012, 8, 467–475. [Google Scholar] [CrossRef]
  9. Massey, L.K.; Roman-Smith, H.; Sutton, R.A. Effect of dietary oxalate and calcium on urinary oxalate and risk of formation of calcium oxalate kidney stones. J. Am. Diet Assoc. 1993, 93, 901–906. [Google Scholar] [CrossRef]
  10. Holmes, R.P.; Goodman, H.O.; Assimos, D.G. Contribution of dietary oxalate to urinary oxalate excretion. Kidney Int. 2001, 59, 270–276. [Google Scholar] [CrossRef] [Green Version]
  11. Khan, S.R.; Glenton, P.A.; Byer, K.J. Dietary oxalate and calcium oxalate nephrolithiasis. J. Urol. 2007, 178, 2191–2196. [Google Scholar] [CrossRef]
  12. Dahiya, T.; Pundir, C.S. In vivo oxalate degradation by liposome encapsulated oxalate oxidase in rat model of hyperoxaluria. Indian J. Med. Res. 2013, 137, 136–1341. [Google Scholar] [PubMed]
  13. Kifayatullah, M.; Rahim, H.; Ullah Jan, N.; Abbas, S.; Khan, M.S.; Ikram, M. Anti-urolithiatic effect of Pericampylus glaucus against ethylene glycol induced urolithiasis in male Sprague Dawley rats. Sains Malays. 2019, 48, 1075–1081. [Google Scholar] [CrossRef]
  14. Tiselius, H.G. Epidemiology and medical management of stone disease. Br. J. Urol. Int. 2003, 91, 758–767. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  15. Khan, S.R. Reactive oxygen species, inflammation and calcium oxalate nephrolithiasis. Transl. Androl. Urol. 2014, 3, 256–276. [Google Scholar]
  16. Khan, S.R.; Hackett, R.L. Retention of calcium oxalate crystals in renal tubules. Scanning Microsc. 1991, 5, 707–712. [Google Scholar]
  17. Khan, S.R. Calcium oxalate crystal interaction with renal tubular epithelium, mechanism of crystal adhesion and its impact on stone development. Urol. Res. 1995, 23, 71–79. [Google Scholar] [CrossRef]
  18. Dal Moro, F.; Mancini, M.; Tavolini, I.M.; De Marco, V.; Bassi, P. Cellular and molecular gateways to urolithiasis: A new insight. Urol. Int. 2005, 74, 193–197. [Google Scholar] [CrossRef]
  19. Williams, H.E.; Wandzilak, T.R. Oxalate synthesis, transport and hyperoxaluric syndromes. J. Urol. 1989, 141, 742–749. [Google Scholar] [CrossRef]
  20. Kuhad, A.; Chopra, K. Attenuation of diabetic nephropathy by tocotrienol; involvement of NF-κB signaling pathway. Life Sci. 2009, 84, 296–301. [Google Scholar] [CrossRef]
  21. Grande, M.T.; Pérez-Barriocanal, F.; López-Novoa, J.M. Role of inflammation in túbulo-interstitial damage associated to obstructive nephropathy. J. Inflamm. 2010, 7, 19. [Google Scholar] [CrossRef] [Green Version]
  22. Horuz, R.; Göktaş, C.; Çetinel, C.A.; Akça, O.; Aydın, H.; Ekici, I.D.; Albayrak, S.; Sarıca, K. Role of TNF-associated cytokines in renal tubular cell apoptosis induced by hyperoxaluria. Urolithiasis 2013, 41, 197–203. [Google Scholar] [CrossRef]
  23. Vousden, K.H.; Lane, D.P. P53 in health and disease. Nat. Rev. Mol. Cell Biol. 2007, 8, 275–283. [Google Scholar] [CrossRef]
  24. Jang, J.H.; Surh, Y.J. Potentiation of cellular antioxidant capacity by Bcl-2: Implications for its antiapoptotic function. Biochem. Pharmacol. 2003, 66, 1371–1379. [Google Scholar] [CrossRef]
  25. Shafi, H.; Moazzami, B.; Pourghasem, M.; Kasaeian, A. An overview of treatment options for urinary stones. Casp. J. Intern. Med. 2016, 7, 1–6. [Google Scholar]
  26. Bashir, S.; Gilani, A.H. Antiurolithiatic effect Bergenia ligulata rhizome: An explanation of the underlying mechanisms. J. Ethnopharmacol. 2009, 122, 106–116. [Google Scholar] [CrossRef]
  27. Divakar, K.; Pawar, A.T.; Chandrasekhar, S.B.; Dighe, S.B.; Divakar, G. Protective effect of the hydro-alcoholic extract of Rubia cordifolia roots against ethylene glycol induced urolithiasis in rats. Food Chem. Toxicol. 2010, 48, 1013–1018. [Google Scholar] [CrossRef]
  28. Ahmed, O.; Ahmed, M.; Ragab, M. Antiurolithic and antioxidant influence of Pleurotus ostreatus and Agaricus bisporus aqueous extracts and carvedilol in male rats. Am. J. Biochem. 2015, 5, 99–112. [Google Scholar]
  29. Nirumand, M.C.; Hajialyani, M.; Rahimi, R.; Farzaei, M.H.; Zingue, S. Dietary Plants for the Prevention and Management of Kidney Stones: Preclinical and Clinical Evidence and Molecular Mechanisms. Int. J. Mol. Sci. 2018, 19, 765. [Google Scholar] [CrossRef] [Green Version]
  30. Lindequist, U.; Niedermeyer, T.H.J.; Jülich, W.D. The pharmacological potential of mushrooms. Evid. Based Complement Altern. Med. 2005, 2, 285–299. [Google Scholar] [CrossRef] [Green Version]
  31. Liu, G.; Wang, X. Selection of a culture medium for reducing costs and intracellular polysaccharide production by Agaricus blazei AB2003. Food Technol. Biotechnol. 2005, 47, 210–214. [Google Scholar]
  32. Gordon, M.; Bihari, B.; Goosby, E.; Gorter, R.; Greco, M.; Guralnik, M.; Mimura, T.; Rudinicki, V.; Wong, R.; Kaneko, Y. A placebo controlled trial of the immune modulator, lentinan, in HIV-positive patients: A phase I/II trial. J. Med. 1998, 29, 305–330. [Google Scholar]
  33. Wasser, S.P.; Weis, A.L. Therapeutic effects of substances occurring in higher Basidiomycetes mushrooms: A modern perspective. Crit. Rev. Immunol. 1999, 19, 65–96. [Google Scholar]
  34. Lakhanpal, T.N.; Rana, M. Medicinal and nutraceutical genetic resources of mushrooms. Plant Gene. Resour. Charact. Util. 2005, 3, 288–303. [Google Scholar] [CrossRef]
  35. Katya, K.; Yun, Y.H.; Park, G.; Lee, J.Y.; Yoo, G.; Bai, S.C. Evaluation of the efficacy of fermented by-product of mushroom, Pleurotus ostreatus, as a fish meal replacer in juvenile amur catfish, Silurus asotus: Effects on growth, serological characteristics and immune responses. Asian Australas. J. Anim. Sci. 2014, 27, 1478–1486. [Google Scholar] [CrossRef]
  36. Singh, V.; Vyas, D.; Pandey, R.; Sheikh, I.M. Pleurotus ostreatus produces antioxidant and antiarthritic activity in Wistar albino rats. World J. Pharm. Pharma. Sci. 2015, 4, 1230–1246. [Google Scholar]
  37. Chen, S.; Oh, S.R.; Phung, S.; Hur, G.; Ye, J.J.; Kwok, S.L.; Shrode, G.E.; Belury, M.; Adams, L.S.; Williams, D. Anti-aromatase activity of phytochemicals in white button mushrooms (Agaricus bisporus). Cancer Res. 2006, 66, 12026–12034. [Google Scholar] [CrossRef] [Green Version]
  38. Jeong, S.C.; Jeong, Y.T.; Yang, B.K.; Islam, R.; Koyyalamudi, S.R.; Pang, G.; Cho, K.Y.; Song, C.H. White button mushroom (Agaricus bisporus) lowers blood glucose and cholesterol levels in diabetic and hypercholesterolemic rats. Nutr. Res. 2010, 30, 49–56. [Google Scholar] [CrossRef]
  39. Kozarski, M.; Klaus, A.; Niksic, M.; Jakovljevic, D.; Helsper, J.P.F.G.; van Griensven, L.J.L.D. Antioxidative and immunomodulating activities of polysaccharide extracts of the medicinal mushrooms Agaricus bisporus, Agaricus brasiliensis, Ganoderma lucidum and Phellinus linteus. Food Chem. 2011, 129, 1667–1675. [Google Scholar] [CrossRef]
  40. Moro, C.; Palacios, I.; Lozano, M.; D’Arrigo, M.; Guillamón, E.; Villares, A.; Martinez, J.A.; Garcia-Lafuente, A. Anti-inflammatory activity of methanolic extracts from edible mushrooms in LPS activated RAW 264.7 macrophages. Food Chem. 2012, 130, 350–355. [Google Scholar] [CrossRef]
  41. Feuerstein, G.Z.; Ruffolo, R.R., Jr. Carvedilol, a novel vasodilating beta blocker with the potential for cardiovascular organ protection. Eur. Heart J. 1996, 17 (Suppl. B), 24–29. [Google Scholar] [CrossRef] [Green Version]
  42. de Araújo Júnior, R.F.; Souza, T.O.; de Medeiros, C.A.; de Souza, L.B.; de Freitas, M.L.; de Lucena, H.F.; do Socorro Costa Feitosa Alves, M.; de Araújo, A.A. Carvedilol decrease IL-1β and TNF-ά, inhibits MMP-2, MMP-9, COX-2, and RANKL expression, and up-regulates OPG in a rat model of periodontitis. PLoS ONE 2013, 8, e66391. [Google Scholar] [CrossRef]
  43. Singh, D.; Chander, V.; Chopra, K. Carvedilol and trimetazidine attenuates ferric nitrilotriacetate-induced oxidative renal injury in rats. Toxicology 2003, 191, 143–151. [Google Scholar] [CrossRef]
  44. Hayashi, T.; De Velasco, M.A.; Saitou, Y.; Nose, K.; Nishioka, T.; Ishii, T.; Uemura, H. Carvedilol protects tubular epithelial cells from ischemia-reperfusion injury by inhibiting oxidative stress. Int. J. Urol. 2010, 17, 989–995. [Google Scholar] [CrossRef]
  45. Rodrigues, M.A.C.; da Silva Faria, M.C.; dos Santos, N.A.; Gobe, G.C.; dos Santos, A.C. Carvedilol efficiently protects kidneys without affecting the antitumor efficacy of cisplatin in mice. Chem. Biol. Interact. 2013, 206, 90–99. [Google Scholar] [CrossRef]
  46. Claus, F.D. Pharmacognosy, 4th ed.; Henry Kumpton: London, UK, 1961. [Google Scholar]
  47. El Bohi, K.M.; Hashimoto, Y.; Muzandu, K.; Ikenaka, Y.; Ibrahim, Z.S.; Kazusaka, A.; Fujita, S.; Ishizuka, M. Protective effect of Pleurotus cornucopiae mushroom extract on carbon tetrachloride-induced hepatotoxicity. Jpn. J. Vet. Res. 2009, 57, 109–118. [Google Scholar]
  48. Yamac, M.; Kanbak, G.; Zeytinoglu, M.; Senturk, H.; Bayramoglu, G.; Dokumacioglu, A.; van Griensven, L.J.D. Pancreas protective effect of button mushroom Agaricus bisporus (J. E. Lange) imbach (Agaricomycetidae) extract on rats with streptozotocin-induced diabetes. Int. J. Med. Mushroom 2010, 12, 379–389. [Google Scholar] [CrossRef]
  49. Arozal, W.; Watanabe, K.; Veeraveedu, P.T.; Ma, M.; Thandavarayan, R.A.; Sukumaran, V.; Suzuki, K.; Kodama, M.; Aizawa, Y. Protective effect of carvedilol on daunorubicin-induced cardiotoxicity and nephrotoxicity in rats. Toxicology 2010, 274, 18–26. [Google Scholar] [CrossRef]
  50. Ghaeni, F.A.; Amin, B.; Hariri, A.T.; Meybodi, N.T.; Hosseinzadeh, H. Antilithiatic effects of crocin on ethylene glycol-induced lithiasis in rats. Urolithiasis 2014, 42, 549–558. [Google Scholar] [CrossRef]
  51. Tsuji, H.; Shimizu, N.; Nozawa, M.; Umekawa, T.; Yoshimura, K.; De Velasco, M.A.; Uemura, H.; Khan, S.R. Osteopontin knockdown in the kidneys of hyperoxaluric rats leads to reduction in renal calcium oxalate crystal deposition. Urolithiasis 2014, 42, 195–202. [Google Scholar]
  52. Randhawa, R.; Bhardwaj, R.; Kaur, T. Amelioration of hyperoxaluria-induced kidney dysfunction by chemical chaperone 4-phenylbutyric acid. Urolithiasis 2019, 47, 171–179. [Google Scholar] [CrossRef]
  53. Khan, S.R. Animal models of kidney stone formation: An analysis. World J. Urol. 1997, 15, 236–243. [Google Scholar] [CrossRef] [PubMed]
  54. Huang, H.S.; Ma, M.C.; Chen, J.; Chen, C.F. Changes in the oxidant–antioxidant balance in the kidney of rats with nephrolithiasis induced by ethylene glycol. J. Urol. 2002, 167, 2584–2593. [Google Scholar] [CrossRef]
  55. Murray, R.L. Creatinine. In Clinical Chemistry; Kaplan, A., Pesce, A.J., Eds.; CV Mosby Co.: St Louis, MO, USA, 1984; pp. 1247–1253. [Google Scholar]
  56. Tabacco, A.; Meiattini, F.; Moda, E.; Tarli, P. Simplified enzymic/colorimetric serum urea nitrogen determination. Clin. Chem. 1979, 25, 336–337. [Google Scholar] [CrossRef]
  57. Fossati, P.; Prencipe, L.; Berti, G. Use of 3,5-dichloro-2-hydroxybenzenesulfonic acid/4-aminophenazone chromogenic system in direct enzymic assay of uric acid in serum and urine. Clin. Chem. 1980, 26, 227–231. [Google Scholar] [CrossRef]
  58. Young, D.S. Effects of Drugs on Clinical Laboratory Tests, 5th ed.; American Association for Clinical Chemistry Press: Washington, DC, USA, 2000. [Google Scholar]
  59. Gindler, E.M.; King, J.D. Rapid colorimetric determination of calcium in biologic fluids with methylthymol blue. Am. J. Clin. Pathol. 1972, 58, 376–382. [Google Scholar] [CrossRef]
  60. Bagshaw, S.M.; Bennett, M.; Devarajan, P.; Bellomo, R. Urine biochemistry in septic and non-septic acute kidney injury: A prospective observational study. J. Crit. Care 2013, 28, 371–378. [Google Scholar] [CrossRef] [Green Version]
  61. Banchroft, J.D.; Stevens, A.; Turner, D.R. Theory and Practice of Histological Techniques, 4th ed.; Churchill Livingston: New York, NY, USA; London, UK; San Francisco, CA, USA; Tokyo, Japan, 1996. [Google Scholar]
  62. Gao, H.; Zhou, Y.W. Inhibitory effect of picroside II on hepatocyte apoptosis. Acta Pharmacol. Sin. 2005, 26, 729–736. [Google Scholar] [CrossRef] [Green Version]
  63. Roa, M.; Blane, K.; Zonneberg, M. One-Way Analysis of Variance. PC-STAT, Version IA (C) Copyright; The University of Georgia: Athens, Georgia, 1985. [Google Scholar]
  64. Rathee, D.; Rathee, P.; Rathee, S.; Rathee, D. Phytochemical screening and antimicrobial activity of Picrorrhiza kurroa, an Indian traditional plant used to treat chronic diarrhea. Arab. J. Chem. 2016, 9, S1307–S1313. [Google Scholar] [CrossRef] [Green Version]
  65. Al-Marzoqi, A.H.; Hadi, M.Y.; Hameed, I.H. Determination of metabolites products by Cassia angustifolia and evaluate antimicobial activity. J. Pharmacogn. Phytother. 2016, 8, 25–48. [Google Scholar]
  66. Dardiry, M.H.O.; Mohamed, A.A.A.; Abdelrady, E. Effect of lead (Pb) on phytochemical variability of Jatropha curcas (L.): A versatile perennial of Euphorbiaceae family. J. Biol. Stud. 2018, 1, 133–145. [Google Scholar]
  67. Jin, H.U.; Lee, J.H.; Kim, D.H.; Kim, K.; Lee, G.W.; Choi, S.J.; Chang, P.; Paik, H. Antioxidative and nitric oxide scavenging activity of branched-chain amino acids. Food Sci. Biotechnol. 2015, 24, 1555–1558. [Google Scholar] [CrossRef]
  68. Cecotti, R.; Carpana, E.; Bergomi, P.; Tava, A. Volatile constituents of Trifolium pratense spp. nivale quantified at different growth stages, and evaluation of their antimicrobial activity. Nat. Prod. Commun. 2013, 8, 1625–1628. [Google Scholar] [CrossRef] [Green Version]
  69. Semwal, P.; Painuli, S. Antioxidant, antimicrobial, and GC-MS profiling of Saussurea obvallata (Brahma Kamal) from Uttarakhand Himalaya. Semwal Painuli Clin. Phytosci. 2019, 5, 12. [Google Scholar] [CrossRef] [Green Version]
  70. Moutevelis-Minakakis, P.; Papavassilopoulou, E.; Michas, G.; Georgikopoulou, K.; Ragoussi, M.; Neophytou, N.; Zoumpoulakis, P.; Mavromoustakos, T.; Hadjipavlou-Litina, D. Synthesis, in silico docking experiments of new 2-pyrrolidinone derivatives and study of their anti-inflammatory activity. Bioorg. Med. Chem. 2011, 19, 2888–2902. [Google Scholar] [CrossRef]
  71. Thangam, R.; Suresh, V.; Rajkumar, M.; Vincent, J.D.; Gunasekaran, P.; Anbazhagan, C.; Kaveri, K.; Kannan, S. Antioxidant and in vitro anticancer effect of 2-pyrrolidinone rich fraction of Brassica oleracea var. capitata through induction of apoptosis in human cancer cells. Phytother. Res. 2013, 27, 1664–1670. [Google Scholar] [CrossRef]
  72. Jadeja, R.N.; Powell, F.L.; Martin, P.M. Repurposing fumaric acid esters to treat conditions of oxidative stress and inflammation: A promising emerging approach with broad potential. In Drug Repurposing; Farid, A.B., Ed.; IntechOpen: London, UK, 2020. [Google Scholar] [CrossRef] [Green Version]
  73. Kontogiorgis, C.A.; Hadjipavlou-Litina, D.J.; Schulz, E. Antioxidant activity of DLω-phenyl-amino acid octyl esters with anti-inflammatory activity: Correlation of the structure with lipophilicity. Arzneimittelforschung 2001, 51, 485–488. [Google Scholar]
  74. Lin-Holderer, J.; Li, L.; Gruneberg, D.; Marti, H.H.; Kunze, R. Fumaric acid esters promote neuronal survival upon ischemic stress through activation of the Nrf2 but not HIF-1 signaling pathway. Neuropharmacology 2016, 105, 228–240. [Google Scholar] [CrossRef]
  75. Schulz, E.; Kobow, M.; Sprung, W.D. Analgesic and anti-inflammatory activity of DL-2-(alkoxyphenyl)glycine octyl esters. Agents Actions 1991, 32, 65–66. [Google Scholar] [CrossRef]
  76. Junnila, M.; Rahko, T.; Sukura, A.; Lindberg, L.A. Reduction of carbon tetrachloride-induced hepatotoxic effects by oral administration of betaine in male Han-Wistar rats: A morphometric histological study. Vet. Pathol. 2000, 37, 231–238. [Google Scholar] [CrossRef]
  77. Yokogawa, K.; Watanabe, M.; Takeshita, H.; Nomura, M.; Mano, Y.; Miyamoto, K. Serum aminotransferase activity as a predictor of clearance of drugs metabolized by CYP isoforms in rats with acute hepatic failure induced by carbon tetrachloride. Int. J. Pharma. 2004, 269, 479–489. [Google Scholar] [CrossRef]
  78. Ezeuko, V.C.; Nwokocha, C.R.; Mounmbegna, P.E.; Nriagu, C.C. Effects of Zingiber officinale on liver function of mercuric chloride-induced hepatotoxicity in adult Wistar rats. Electron. J. Biomed. 2007, 3, 40–45. [Google Scholar]
  79. de Water, R.; Noordermeer, C.; van der Kwast, T.H.; Nizze, H.; Boevé, E.R.; Kok, D.J.; Schröder, F.H. Calcium oxalate nephrolithiasis: Effect of renal crystal deposition on the cellular composition of the renal interstitium. Am. J. Kidney Dis. 1999, 33, 761–771. [Google Scholar] [CrossRef]
  80. Lulat, S.I.; Yadav, Y.C.; Balaraman, R.; Maheshwari, R. Antiurolithiatic effect of lithocare against ethylene glycol-induced urolithiasis in Wistar rats. J. Pharmacol. 2016, 48, 78–82. [Google Scholar]
  81. Wang, J.; Zhang, Q.; Jin, W.; Niu, X.; Zhang, H. Effects and mechanism of low molecular weight fucoidan in mitigating the peroxidative and renal damage induced by adenine. Carbohydr. Polym. 2011, 84, 417–423. [Google Scholar] [CrossRef]
  82. Saeidi, J.; Bozorgi, H.; Zendehdel, A.; Mehrzad, J. Therapeutic effects of aqueous extracts of Petroselinum sativum on ethylene glycol-induced kidney calculi in rats. Urol. J. 2012, 9, 361–366. [Google Scholar]
  83. Aggarwal, D.; Kaushal, R.; Kaur, T.; Bijarnia, R.K.; Puri, S.; Singla, S.K. The most potent antilithiatic agent ameliorating renal dysfunction and oxidative stress from Bergenia ligulata rhizome. J. Ethnopharmacol. 2014, 158, 85–93. [Google Scholar] [CrossRef]
  84. Noorafshan, A.; Karbalay-Doust, S.; Karimi, F. Diosmin reduces calcium oxalate deposition and tissue degeneration in nephrolithiasis in rats: A stereological study. Korean J. Urol. 2013, 54, 252–257. [Google Scholar] [CrossRef]
  85. Heather, M.; David, W.; Andrew, J. Macrophages and the kidney. Hypertension 2004, 13, 285–290. [Google Scholar]
  86. Sirag, H.M. Biochemical and Hematological Studies for the Protective effect of oyster mushroom (Pleurotus ostreatus) against glycerol-induced acute renal failure in rats. J. Biol. Sci. 2009, 9, 746–752. [Google Scholar] [CrossRef] [Green Version]
  87. Yoon, H.J.; Moon, M.E.; Park, H.S.; Kim, H.W.; Im, S.Y.; Lee, J.H.; Kim, Y.H. Effects of chitosan oligosaccharide (COS) on the glycerol-induced acute renal failure in vitro and in vivo. Food Chem. Toxicol. 2008, 46, 710–716. [Google Scholar] [CrossRef]
  88. Shah, J.G.; Patel, B.G.; Patel, S.B.; Patel, R.K. Antiurolithiatic and antioxidant activity of Hordeum vulgare seeds on ethylene glycol-induced urolithiasis in rats. Indian J. Pharmacol. 2012, 44, 672–677. [Google Scholar] [CrossRef]
  89. Ahmed, A.; Wadud, A.; Jahan, N.; Bilal, A.; Hajera, S. Efficacy of Adiantum capillus veneris Linn in chemically induced urolithiasis in rats. J. Ethnopharmacol. 2013, 146, 411–416. [Google Scholar] [CrossRef]
  90. Bijarnia, R.K.; Bachtler, M.; Chandak, P.G.; van Goor, H.; Pasch, A. Sodium thiosulfate ameliorates oxidative stress and preserves renal function in hyperoxaluric rats. PLoS ONE 2015, 10, e0124881. [Google Scholar] [CrossRef]
  91. Adeneye, A.A.; Benebo, A.S. Protective effect of the aqueous leaf and seed extract of Phyllanthus amarus on gentamicin and acetaminophen-induced nephrotoxic rats. J. Ethnopharmacol. 2008, 118, 318–323. [Google Scholar] [CrossRef]
  92. Kim, H.Y.; Yokozawa, T.; Nakagawa, T.; Sasaki, S. Protective effect of gamma-aminobutyric acid against glycerol-induced acute renal failure in rats. Food Chem. Toxicol. 2004, 42, 2009–2014. [Google Scholar] [CrossRef]
  93. He, L.; Shen, P.; Fu, Q.; Li, J.; Dan, M.; Wang, X.; Jia, W. Nephro-protective effect of Kangqianling decoction on chronic renal failure rats. J. Ethnopharmacol. 2009, 122, 367–373. [Google Scholar] [CrossRef] [Green Version]
  94. Ghodasara, J.; Pawar, A.; Deshmukh, C.; Kuchekar, B. Inhibitory effect of rutin and curcumin on experimentally-induced calcium oxalate urolithiasis in rats. Pharmacogn. Res. 2010, 2, 388–392. [Google Scholar]
  95. Siener, R. Impact of dietary habits on stone incidence. Urol. Res. 2006, 34, 131–133. [Google Scholar] [CrossRef]
  96. Selvam, R.; Kalaiselvi, P.; Govindaraj, A.; Murugan, V.M.; Satish Kumar, A.S. Effect of A. lanata leaf extract and Vediuppu chunnam on the urinary risk factors of calcium oxalate urolithiasis during experimental hyperoxaluria. Pharmacol. Res. 2001, 43, 89–93. [Google Scholar] [CrossRef]
  97. Soundararajan, P.; Mahesh, R.; Ramesh, T.; Begum, V.H. Effect of Aerva lanata on calcium oxalate urolithiasis in rats. Indian J. Exp. Biol. 2006, 44, 981–986. [Google Scholar]
  98. Naguib, Y.M.; Azmy, R.M.; Samaka, R.M.; Salem, M.F. Pleurotus ostreatus opposes mitochondrial dysfunction and oxidative stress in acetaminophen-induced hepato-renal injury. BMC Complement. Altern. Med. 2014, 14, 494. [Google Scholar] [CrossRef]
  99. Rajasekar, R.; Jayaprakash, K. Protective effect of Agaricus bisporus (Button mushroom) on cisplatin induced nephrotoxicity in albino rats. World J. Pharmacol. Sci. 2016, 4, 366–372. [Google Scholar]
  100. Hart, P.D.; Bakris, G.L. Should β-blockers be used to control hypertension in people with chronic kidney disease? Semin. Nephrol. 2007, 27, 555–564. [Google Scholar] [CrossRef]
  101. Carvalho Rodrigues, M.A.; Rodrigues, J.L.; Martins, N.M.; Barbosa, F.; Curti, C.; Santos, N.A.G.; Santos, A.C. Carvedilol protects against cisplatin-induced oxidative stress, redox state unbalance and apoptosis in rat kidney mitochondria. Chem. Biol. Interact. 2011, 189, 45–51. [Google Scholar] [CrossRef]
  102. Gadge, N.B.; Jalalpure, S.S. Curative treatment with extracts of Bombax ceiba fruit reduces risk of calcium oxalate urolithiasis in rats. Pharma. Biol. 2012, 50, 310–317. [Google Scholar] [CrossRef]
  103. Patel, P.K.; Patel, M.A.; Vyas, B.A.; Shah, D.R.; Gandhi, T.R. Antiurolithiatic activity of saponin rich fraction from the fruits of Solanum xanthocarpum Schrad. & Wendl. (Solanaceae) against ethylene glycol induced urolithiasis in rats. J. Ethnopharmacol. 2012, 144, 160–170. [Google Scholar]
  104. Bodakhe, K.S.; Namdeo, K.P.; Patra, K.C.; Machwal, L.; Pareta, S.K. A polyherbal formulation attenuates hyperoxaluria-induced oxidative stress and prevents subsequent deposition of calcium oxalate crystals and renal cell injury in rat kidneys. Chin. J. Nat. Med. 2013, 11, 466–471. [Google Scholar] [CrossRef]
  105. Saha, S.; Shrivastav, P.S.; Verma, R.J. Antioxidative mechanism involved in the preventive efficacy of Bergenia ciliata rhizomes against experimental nephrolithiasis in rats. Pharm. Biol. 2014, 52, 712–722. [Google Scholar] [CrossRef]
  106. Karadi, R.V.; Gadge, N.B.; Alagawadi, K.R.; Savadi, R.V. Effect of Moringa oleifera Lam. root-wood on ethylene glycol induced urolithiasis in rats. J. Ethnopharmacol. 2006, 105, 306–311. [Google Scholar] [CrossRef]
  107. Freitas, A.M.; Schor, N.; Boim, M.A. The effect of Phyllanthus niruri on urinary inhibitors of calcium oxalate crystallization and other factors associated with renal stone formation. Br. J. Urol. Int. 2002, 89, 829–834. [Google Scholar] [CrossRef] [Green Version]
  108. Thamilselvan, S.; Khan, S.R.; Menon, M. Oxalate and calcium oxalate mediated free radical toxicity in renal epithelial cells: Effect of antioxidants. Urol. Res. 2003, 31, 3–9. [Google Scholar] [CrossRef] [PubMed]
  109. Scheid, C.R.; Cao, L.C.; Honeyman, T.; Jonassen, J.A. How elevated oxalate can promote kidney stone disease: Changes at the surface and in the cytosol of renal cells that promote crystal adherence and growth. Front. Biosci. 2004, 9, 797–808. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  110. Kandhare, A.D.; Patil, M.V.K.; Bodhankar, S.L. l-Arginine attenuates the ethylene glycol induced urolithiasis in ininephrectomized hypertensive rats: Role of KIM-1, NGAL, and NOs. Ren. Fail. 2015, 37, 709–721. [Google Scholar] [CrossRef] [Green Version]
  111. Cruzan, G.; Corley, R.A.; Hard, G.C.; Mertens, J.J.; McMartin, K.E.; Snellings, W.M.; Gingell, R.; Deyo, J.A. Subchronic toxicity of ethylene glycol in Wistar and F-344 rats related to metabolism and clearance of metabolites. Toxicol. Sci. 2004, 81, 502–511. [Google Scholar] [CrossRef] [Green Version]
  112. Khan, A.; Bashir, S.; Khan, S.R.; Gilani, A.H. Antiurolithic activity of Origanum vulgare is mediated through multiple pathways. BMC Complement. Altern. Med. 2011, 11, 96. [Google Scholar] [CrossRef] [Green Version]
  113. Khan, S.R.; Glenton, P.A.; Byer, K.J. Modeling of hyperoxaluric calcium oxalate nephrolithiasis: Experimental induction of hyperoxaluria by hydroxy-L-proline. Kidney Int. 2006, 70, 914–923. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  114. Kaur, T.; Bijarnia, R.K.; Singla, S.K.; Tandon, C. In vivo efficacy of Trachyspermum ammi anticalcifying protein in urolithiatic rat model. J. Ethnopharmacol. 2009, 126, 459–462. [Google Scholar] [CrossRef]
  115. Pawar, A.T.; Gaikwad, G.D.; Metkari, K.S.; Tijore, K.A.; Ghodasara, J.V.; Kuchekar, B.S. Effect of Terminalia chebula fruit extract on ethylene glycol induced urolithiasis in rats. Biomed. Aging Pathol. 2012, 2, 99–103. [Google Scholar] [CrossRef]
  116. Makasana, A.; Ranpariya, V.; Desai, D.; Mendpara, J.; Parekh, V. Evaluation for the anti-urolithiatic activity of Launaea procumbens against ethylene glycol-induced renal calculi in rats. Toxicol. Rep. 2014, 1, 46–52. [Google Scholar] [CrossRef] [Green Version]
  117. Li, X.; Liang, Q.; Sun, Y.; Diao, L.; Qin, Z.; Wang, W.; Lu, J.; Fu, S.; Ma, B.; Yue, Z. Potential mechanisms responsible for the antinephrolithic effects of an aqueous extract of Fructus aurantii. Evid. Based Complement. Altern. Med. 2015, 2015, 491409. [Google Scholar] [CrossRef] [Green Version]
  118. Bashir, S.; Gilani, A.H. Antiurolithic effect of berberine is mediated through multiple pathways. Eur. J. Pharmacol. 2011, 651, 168–175. [Google Scholar] [CrossRef] [PubMed]
  119. Corley, R.A.; Wilson, D.M.; Hard, G.C.; Stebbins, K.E.; Bartels, M.J.; Soelberg, J.J.; Dryzga, M.D.; Gingell, R.; McMartin, K.E.; Snellings, W.M. Dosimetry considerations in the enhanced sensitivity of male Wistar rats to chronic ethylene glycol-induced nephrotoxicity. Toxicol. Appl. Pharmacol. 2008, 228, 165–178. [Google Scholar] [CrossRef] [PubMed]
  120. Hackett, R.L.; Shevock, P.N.; Khan, S.R. Alteration in MDCK and LLC-PK1 cells exposed to oxalate and calcium oxalate monohydrate crystals. Scanning Microsc. 1995, 9, 587–596. [Google Scholar] [PubMed]
  121. Scheid, C.R.; Koul, H.K.; Kennington, L.; Hill, W.A.; Luber-Narod, J.; Jonassen, J.; Honeyman, T.; Menon, M. Oxalate-induced damage to renal tubular cells. Scanning Microsc. 1995, 9, 1097–1105. [Google Scholar]
  122. Gilmore, T.D. Introduction to NF-κB: Players, pathways, perspectives. Oncogene 2006, 25, 6680–6684. [Google Scholar] [CrossRef] [Green Version]
  123. Sanz, A.B.; Sanchez-Niño, M.D.; Ramos, A.M.; Moreno, J.A.; Santamaria, B.; Ruiz-Ortega, M.; Egido, J.; Ortiz, A. NF-κB in renal inflammation. J. Am. Soc. Nephrol. 2010, 21, 1254–1262. [Google Scholar] [CrossRef] [Green Version]
  124. Perkins, N.D. Integrating cell-signalling pathways with NF-κB and IKK function. Nat. Rev. Mol. Cell Biol. 2007, 8, 49–62. [Google Scholar] [CrossRef]
  125. Brasier, A.R. The NF-κB regulatory network. Cardiovasc. Toxicol. 2006, 6, 111–130. [Google Scholar] [CrossRef]
  126. Schreck, R.; Peter Rieber, P.; Baeuerle, P.A. Reactive oxygen intermediates as apparently widely used messengers in the activation of the NF-κB transcription factor and HIV-1. EMBO J. 1991, 10, 2247–2258. [Google Scholar] [CrossRef]
  127. Tak, P.P.; Firestein, G.S. NF-κB: A key role in inflammatory diseases. J. Clin. Investig. 2001, 107, 7–11. [Google Scholar] [CrossRef]
  128. Jost, P.J.; Ruland, J. Aberrant NF-κB signaling in lymphoma: Mechanisms, consequences, and therapeutic implications. Blood 2007, 109, 2700–2707. [Google Scholar] [CrossRef] [Green Version]
  129. Garufi, A.; Ubertini, V.; Mancini, F.; D’Orazi, V.; Baldari, S.; Moretti, F.; Bossi, G.; D’Orazi1, G. The beneficial effect of Zinc (II) on low-dose chemotherapeutic sensitivity involves p53 activation in wild-type p53-carrying colorectal cancer cells. J. Exp. Clin. Cancer Res. 2015, 34, 87. [Google Scholar] [CrossRef] [Green Version]
  130. Ahmed, O.M.; Fahim, H.I.; Ahmed, H.Y.; Al-Muzafar, H.M.; Ahmed, R.R.; Amin, K.A.; El-Nahass, E.; Abdelazeem, W.H. The preventive effects and the mechanisms of action of navel orange peel hydroethanolic extract, naringin, and naringenin in N-acetyl-p-aminophenol-induced liver Injury in Wistar rats. Oxid. Med. Cell. Longev. 2019, 2019, 2745352. [Google Scholar] [CrossRef] [Green Version]
  131. Ahmed, O.M.; Ali, T.M.; Abdel Gaid, M.A.; Elberry, A.A. Effects of enalapril and paricalcitol treatment on diabetic nephropathy and renal expressions of TNF-α, p53, caspase-3 and Bcl-2 in STZ-induced diabetic rats. PLoS ONE 2019, in press. [Google Scholar]
  132. Borghetti, G.; Yamaguchi, A.A.; Aikawa, J.; Yamazaki, R.K.; Pereira de Brito, G.A.; Luiz Claudio Fernandes, L.C. Fish oil administration mediates apoptosis of Walker 256 tumor cells by modulation of p53, Bcl-2, caspase-7 and caspase-3 protein expression. Lipids Health Dis. 2015, 14, 94. [Google Scholar] [CrossRef] [Green Version]
  133. Nakazawa, K.; Dashzeveg, N.; Yoshida, K. Tumor suppressor p53 induces miR-1915 processing to inhibit Bcl-2 in the apoptotic response to DNA damage. FEBS J. 2014, 281, 2937–2944. [Google Scholar] [CrossRef]
  134. Barkett, M.; Gilmore, T.D. Control of apoptosis by Rel/NF-κB transcription factors. Oncogene 1999, 18, 6910–6924. [Google Scholar] [CrossRef] [Green Version]
  135. Ashikawa, K.; Shishodia, S.; Fokt, I.; Priebe, W.; Aggarwal, B.B. Evidence that activation of nuclear factor-kappaB is essential for the cytotoxic effects of doxorubicin and its analogues. Biochem. Pharmacol. 2004, 67, 353–364. [Google Scholar] [CrossRef]
  136. Campbell, K.J.; Rocha, S.; Perkins, N.D. Active repression of antiapoptotic gene expression by RelA(p65) NF-kappa B. Mol. Cell. 2004, 13, 853–865. [Google Scholar] [CrossRef]
  137. Ho, W.C.; Dickson, K.M.; Barker, P.A. Nuclear factor-kappaB induced by doxorubicin is deficient in phosphorylation and acetylation and represses nuclear factor-kappaB-dependent transcription in cancer cells. Cancer Res. 2005, 65, 4273–4281. [Google Scholar] [CrossRef] [Green Version]
  138. Bednarski, B.K.; Baldwin, A.S., Jr.; Kim, H.J. Addressing reported pro-apoptotic functions of NF-kB:targeted inhibition of canonical NF-kB enhances the apoptotic effects of doxorubicin. PLoS ONE 2009, 4, e6992. [Google Scholar] [CrossRef] [Green Version]
  139. Parrondo, R.; de las Pozas, A.; Reiner, T.; Rai, P.; Perez-Stable, C. NF-κB activation activation enhances cell death by antimitotic drugs in human prostate cancer cells. Mol. Cancer 2010, 9, 182. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  140. Mehmet, N.M.; Ender, O. Effect of urinary stone disease and its treatment on renal function. World J. Nephrol. 2015, 4, 271–276. [Google Scholar] [CrossRef] [PubMed]
  141. Joshi, S.; Wang, W.; Peck, A.B.; Khan, S.R. Activation of the NLRP3 inflammasome in association with calcium oxalate crystal induced reactive oxygen species in kidneys. J. Urol. 2015, 193, 1684–1691. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  142. Sahin, C.; Sarikaya, S.; Basak, K.; Cetinel, C.A.; Narter, F.; Eryildirim, B.; Saglam, E.; Sarica, K. Limitation of apoptotic changes and crystal deposition by Tutukon following hyperoxaluria-induced tubular cell injury in rat model. Urolithisasis 2015, 43, 313–322. [Google Scholar] [CrossRef] [PubMed]
  143. Lu, X.; Gao, B.; Wang, Y.; Liu, Z.; Yasui, T.; Liu, P.; Liu, J.; Emmanuel, N.; Zhu, Q.; Xiao, C. Renal tubular epithelial cell injury, apoptosis and inflammation are involved in melamine-related kidney stone formation. Urol. Res. 2012, 40, 717–723. [Google Scholar] [CrossRef]
  144. Hu, H.; Chen, W.; Ding, J.; Jia, M.; Yin, J.; Guo, Z. Fasudil prevents calcium oxalate crystal deposit and renal fibrogenesis in glyoxylate-induced nephrolithic mice. Exp. Mol. Pathol. 2015, 98, 277–285. [Google Scholar] [CrossRef]
  145. Hsieh, N.; Shih, C.H.; Chen, H.Y. Effects of Tamm-Horsfall protein on the protection of MCDK cells from oxalate induced free radical injury. Urol. Res. 2003, 31, 10–16. [Google Scholar] [CrossRef]
  146. Jedinak, A.; Dudhgaonkar, S.; Wu, Q.; Simon, J.; Sliva, D. Anti-inflammatory activity of edible oyster mushroom is mediated through the inhibition of NF-κB and AP-1 signaling. Nutr. J. 2011, 2011, 10–52. [Google Scholar] [CrossRef] [Green Version]
  147. Amstad, P.A.; Liu, H.; Ichimiya, M.; Berezesky, I.K.; Trump, B.F.; Buhimschi, I.A.; Gutierrez, P.L. BCL-2 is involved in preventing oxidant-induced cell death and in decreasing oxygen radical production. Redox Rep. 2001, 6, 351–362. [Google Scholar] [CrossRef]
  148. Volman, J.J.; Helsper, J.P.; Wei, S.; Baars, J.J.; van Griensven, L.J.; Sonnenberg, A.S.; Mensink, R.P.; Plat, J. Effects of mushroom-derived beta-glucan-rich polysaccharide extracts on nitric oxide production by bone marrow-derived macrophages and nuclear factor-kappaB transactivation in Caco-2 reporter cells: Can effects be explained by structure? Mol. Nut. Food Res. 2010, 54, 268–276. [Google Scholar] [CrossRef]
  149. Arab, H.H.; El-Sawalhi, M.M. Carvedilol alleviates adjuvant-induced arthritis and subcutaneous air pouch edema: Modulation of oxidative stress and inflammatory mediators. Toxicol. Appl. Pharmacol. 2013, 268, 241–248. [Google Scholar] [CrossRef] [PubMed]
  150. Yasar, A.; Erdemir, F.; Parlaktas, B.S.; Atilgan, D.; Koseoglu, R.D.; Saylan, O.; Firat, F. The effect of carvedilol on serum and tissue oxidative stress parameters in partial ureteral obstruction induced rat model. Kaohsiung J. Med. Sci. 2013, 29, 19–25. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  151. Yuan, Z.; Shioji, K.; Kihara, Y.; Takenaka, H.; Onozawa, Y.; Kishimoto, C. Cardioprotective effects of carvedilol on acute autoimmune myocarditis: Anti-inflammatory effects associated with antioxidant property. Am. J. Physiol. Heart Circ. Physiol. 2004, 286, H83–H90. [Google Scholar] [CrossRef]
  152. Sahu, B.D.; Koneru, M.; Bijargi, S.R.; Kota, A.; Sistla, R. Chromium-induced nephrotoxicity and ameliorative effect of carvedilol in rats: Involvement of oxidative stress, apoptosis and inflammation. Chem. Biol. Interact. 2014, 223, 69–79. [Google Scholar] [CrossRef] [PubMed]
Biomolecules 10 01317 g001 550
Figure 1. P. ostreatus (A); and A. bisporus (B).
Figure 1. P. ostreatus (A); and A. bisporus (B).
Biomolecules 10 01317 g001
Biomolecules 10 01317 g002 550
Figure 2. GC-MS analysis of P. ostreatus aqueous extract.
Figure 2. GC-MS analysis of P. ostreatus aqueous extract.
Biomolecules 10 01317 g002
Biomolecules 10 01317 g003 550
Figure 3. GC-MS analysis of A. bisporus aqueous extract.
Figure 3. GC-MS analysis of A. bisporus aqueous extract.
Biomolecules 10 01317 g003
Biomolecules 10 01317 g004 550
Figure 4. Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on body weight, kidney weight and relative kidney weight of ethylene glycol-administered rats. For each parameter, means which share the same letter(s) are not significantly different.
Figure 4. Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on body weight, kidney weight and relative kidney weight of ethylene glycol-administered rats. For each parameter, means which share the same letter(s) are not significantly different.
Biomolecules 10 01317 g004
Biomolecules 10 01317 g005 550
Figure 5. Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on levels of serum parameters related to kidney function of ethylene glycol-administered rats. For each parameter, means which share the same letter(s) are not significantly different.
Figure 5. Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on levels of serum parameters related to kidney function of ethylene glycol-administered rats. For each parameter, means which share the same letter(s) are not significantly different.
Biomolecules 10 01317 g005
Biomolecules 10 01317 g006 550
Figure 6. Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on different urine parameters related to renal efficiency of ethylene glycol-administered rats. For each parameter, means which share the same letter(s) are not significantly different.
Figure 6. Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on different urine parameters related to renal efficiency of ethylene glycol-administered rats. For each parameter, means which share the same letter(s) are not significantly different.
Biomolecules 10 01317 g006
Biomolecules 10 01317 g007 550
Figure 7. Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on various ratios related to kidney function of ethylene glycol-administered rats. For each parameter, means which share the same letter(s) are not significantly different.
Figure 7. Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on various ratios related to kidney function of ethylene glycol-administered rats. For each parameter, means which share the same letter(s) are not significantly different.
Biomolecules 10 01317 g007
Biomolecules 10 01317 g008 550
Figure 8. Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on serum, kidney and urine oxalate levels in ethylene glycol-administered rats. For each parameter, means which share the same letter(s) are not significantly different.
Figure 8. Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on serum, kidney and urine oxalate levels in ethylene glycol-administered rats. For each parameter, means which share the same letter(s) are not significantly different.
Biomolecules 10 01317 g008
Biomolecules 10 01317 g009 550
Figure 9. Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on urine specific gravity in ethylene glycol-administered rats. Means which share the same letter(s) are not significantly different.
Figure 9. Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on urine specific gravity in ethylene glycol-administered rats. Means which share the same letter(s) are not significantly different.
Biomolecules 10 01317 g009
Biomolecules 10 01317 g010 550
Figure 10. Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on kidney calcium content in ethylene glycol-administered rats. Means which share the same letter(s) are not significantly different.
Figure 10. Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on kidney calcium content in ethylene glycol-administered rats. Means which share the same letter(s) are not significantly different.
Biomolecules 10 01317 g010
Biomolecules 10 01317 g011 550
Figure 11. Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on serum TNF-α and IL-1β levels in ethylene glycol-administered rats. Means which share the same letter(s) are not significantly different.
Figure 11. Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on serum TNF-α and IL-1β levels in ethylene glycol-administered rats. Means which share the same letter(s) are not significantly different.
Biomolecules 10 01317 g011
Biomolecules 10 01317 g012 550
Figure 12. Photomicrographs of haematoxylin and eosin stained sections of kidney of a normal control rat showing normal histological structure of the medullary portion and the tubules (T) (a) (×256), normal histological structure of the cortex portion containing glomerulus (G) and tubule (T) (b) (×128) and normal histological structure of the renal parenchyma where glomerulus (G), proximal tubule (PT) and distal tubule (DT) were observed (c) (×400).
Figure 12. Photomicrographs of haematoxylin and eosin stained sections of kidney of a normal control rat showing normal histological structure of the medullary portion and the tubules (T) (a) (×256), normal histological structure of the cortex portion containing glomerulus (G) and tubule (T) (b) (×128) and normal histological structure of the renal parenchyma where glomerulus (G), proximal tubule (PT) and distal tubule (DT) were observed (c) (×400).
Biomolecules 10 01317 g012
Biomolecules 10 01317 g013 550
Figure 13. Photomicrographs of hematoxylin and eosin stained sections of kidney of ethylene glycol control rat showing atrophy (A) and congestion (CG) of the glomerular tufts and presence of protein casts (PC) in the lumen of the renal tubules (a) (×400); interstitial nephritis marked by inflammatory cell (IC) infiltration and cellular casts (CC) in the lumen of the renal tubules and glomerular hemorrhage (GH) (b) (×400); necrosis (nc) of renal tubules and presence of oxalate crystals (arrows) in the lumen of the renal tubules (c) (×400); dysplastic tubular cells (D) and focal necrosis (nc) of the renal tubules associated with massive inflammatory cells (IC) infiltration (d) (×400); enlarged vesicular nuclei (vn) with irregular arrangement (dysplasia and anaplasia) (D) in the lining epithelium of the renal tubules (e) (×256); and cystic dilatation (CD) of the renal tubules, focal inflammatory cells (IC) infiltration, necrosis (nc) and apoptotic cells (AP) (f) (×400).
Figure 13. Photomicrographs of hematoxylin and eosin stained sections of kidney of ethylene glycol control rat showing atrophy (A) and congestion (CG) of the glomerular tufts and presence of protein casts (PC) in the lumen of the renal tubules (a) (×400); interstitial nephritis marked by inflammatory cell (IC) infiltration and cellular casts (CC) in the lumen of the renal tubules and glomerular hemorrhage (GH) (b) (×400); necrosis (nc) of renal tubules and presence of oxalate crystals (arrows) in the lumen of the renal tubules (c) (×400); dysplastic tubular cells (D) and focal necrosis (nc) of the renal tubules associated with massive inflammatory cells (IC) infiltration (d) (×400); enlarged vesicular nuclei (vn) with irregular arrangement (dysplasia and anaplasia) (D) in the lining epithelium of the renal tubules (e) (×256); and cystic dilatation (CD) of the renal tubules, focal inflammatory cells (IC) infiltration, necrosis (nc) and apoptotic cells (AP) (f) (×400).
Biomolecules 10 01317 g013
Biomolecules 10 01317 g014 550
Figure 14. Photomicrographs of hematoxylin and eosin stained sections of kidney of ethylene glycol-administered rat treated with P. ostreatus aqueous extract showing homogenous eosinophilic casts (EC) in the lumen of few medullary tubules (a) (×256), slight congestion (C) of intertubular blood capillaries (b) (×400); congestion (C) of intertubular blood vessles (c) (×400); slight congestion of the glomrular tufts (CG) (d) (×400); and congestion (C) in the cortical blood vessels and glomeruli (CG) with perivascular inflammatory cells (IC) infiltration and oedema (O) (e) (×128).
Figure 14. Photomicrographs of hematoxylin and eosin stained sections of kidney of ethylene glycol-administered rat treated with P. ostreatus aqueous extract showing homogenous eosinophilic casts (EC) in the lumen of few medullary tubules (a) (×256), slight congestion (C) of intertubular blood capillaries (b) (×400); congestion (C) of intertubular blood vessles (c) (×400); slight congestion of the glomrular tufts (CG) (d) (×400); and congestion (C) in the cortical blood vessels and glomeruli (CG) with perivascular inflammatory cells (IC) infiltration and oedema (O) (e) (×128).
Biomolecules 10 01317 g014
Biomolecules 10 01317 g015 550
Figure 15. Photomicrographs of hematoxylin and eosin stained sections of kidney of ethylene glycol-administered rat treated with A. bisporus aqueous extract showing few red blood cells (BC) in the tubular lumen and in between the tubules at the medulla (a) (×256); normal renal structure with slight glomerular congestion (CG) (b) (×400); congestion (C) of renal blood vessels and glomeruli (CG) (c) (×400); and small protein casts (PC) in the lumen of some renal tubules and mild congestion in the glomeruli (CG) (d) (×400).
Figure 15. Photomicrographs of hematoxylin and eosin stained sections of kidney of ethylene glycol-administered rat treated with A. bisporus aqueous extract showing few red blood cells (BC) in the tubular lumen and in between the tubules at the medulla (a) (×256); normal renal structure with slight glomerular congestion (CG) (b) (×400); congestion (C) of renal blood vessels and glomeruli (CG) (c) (×400); and small protein casts (PC) in the lumen of some renal tubules and mild congestion in the glomeruli (CG) (d) (×400).
Biomolecules 10 01317 g015
Biomolecules 10 01317 g016 550
Figure 16. Photomicrographs of hematoxylin and eosin stained sections of kidney of ethylene glycol-administered rat treated with carvedilol showing red blood cells (BC) in some of the tubular lumen at the medulla (a) (×256); slight congestion (C) in the cortical blood vessels and glomeruli (CG) (b) (×128); vacuolization (V) of epithelial lining the tubules (c) (×400); and hypertrophy and vacuolization (V) of the glomerular tufts, vacuolization of epithelial lining renal tubules and perivascular inflammatory cells (IC) infiltration (d) (×400).
Figure 16. Photomicrographs of hematoxylin and eosin stained sections of kidney of ethylene glycol-administered rat treated with carvedilol showing red blood cells (BC) in some of the tubular lumen at the medulla (a) (×256); slight congestion (C) in the cortical blood vessels and glomeruli (CG) (b) (×128); vacuolization (V) of epithelial lining the tubules (c) (×400); and hypertrophy and vacuolization (V) of the glomerular tufts, vacuolization of epithelial lining renal tubules and perivascular inflammatory cells (IC) infiltration (d) (×400).
Biomolecules 10 01317 g016
Biomolecules 10 01317 g017 550
Figure 17. Photomicrographs (a–e) of immunohistochemically stained kidney sections. Images showed the higher amount of NF-κB (yellowish brown color) in cytoplasm and nuclei of ethylene glycol control group (b) (×384) as compared with normal control rats (a) (×384). The treatment of ethylene glycol administered rats with P. ostreatus (c) (×384) and A. bisporus (d) (×384) infusions and carvedilol (e) (×384) markedly decreased the dark brownish color of NF-κB.
Figure 17. Photomicrographs (a–e) of immunohistochemically stained kidney sections. Images showed the higher amount of NF-κB (yellowish brown color) in cytoplasm and nuclei of ethylene glycol control group (b) (×384) as compared with normal control rats (a) (×384). The treatment of ethylene glycol administered rats with P. ostreatus (c) (×384) and A. bisporus (d) (×384) infusions and carvedilol (e) (×384) markedly decreased the dark brownish color of NF-κB.
Biomolecules 10 01317 g017
Biomolecules 10 01317 g018 550
Figure 18. Photomicrographs (a–e) of immunohistochemically stained kidney sections showing the greater amount of the apoptotic marker p53 (yellowish brown color) in the cytoplasm and nuclei of the hyperoxaluric control rats (b) (×384) as compared with normal control group (a) (×384). The p53 was remarkably decreased after treatment of ethylene glycol-administered rats with P. ostreatus (c) (×384) and A. bisporus (d) (×384) infusions and carvedilol (e) (×384), which was indicated by decline of the intensity of yellowish brown color.
Figure 18. Photomicrographs (a–e) of immunohistochemically stained kidney sections showing the greater amount of the apoptotic marker p53 (yellowish brown color) in the cytoplasm and nuclei of the hyperoxaluric control rats (b) (×384) as compared with normal control group (a) (×384). The p53 was remarkably decreased after treatment of ethylene glycol-administered rats with P. ostreatus (c) (×384) and A. bisporus (d) (×384) infusions and carvedilol (e) (×384), which was indicated by decline of the intensity of yellowish brown color.
Biomolecules 10 01317 g018
Biomolecules 10 01317 g019 550
Figure 19. Photomicrographs of immunohistochemically stained kidney sections showing the lighter amount of the antiapoptotic marker Bcl-2 (yellowish brown color) in the cytoplasm of the urolithic rats (b) (×512) as compared with normal control group (a) (×512). Bcl-2 was potentially increased after treatment of ethylene glycol-administered rats with P. ostreatus (c) (×512), A. bisporus (d) (×512) and carvedilol (e) (×512), which was indicated by increase of intensity of the yellowish brown color.
Figure 19. Photomicrographs of immunohistochemically stained kidney sections showing the lighter amount of the antiapoptotic marker Bcl-2 (yellowish brown color) in the cytoplasm of the urolithic rats (b) (×512) as compared with normal control group (a) (×512). Bcl-2 was potentially increased after treatment of ethylene glycol-administered rats with P. ostreatus (c) (×512), A. bisporus (d) (×512) and carvedilol (e) (×512), which was indicated by increase of intensity of the yellowish brown color.
Biomolecules 10 01317 g019
Biomolecules 10 01317 g020 550
Figure 20. Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on percent area of yellowish brown color of NF-κB, p53 and Bcl-2 expressions detected by image analysis of immunohistochemically stained kidney sections in ethylene glycol-administered rats. For each mediator, three kidney sections from three rats of each group were immunohistochemically stained and were subjected to ImageJ analysis. For each parameter, means which share the same superscript letter(s) are not significantly different.
Figure 20. Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on percent area of yellowish brown color of NF-κB, p53 and Bcl-2 expressions detected by image analysis of immunohistochemically stained kidney sections in ethylene glycol-administered rats. For each mediator, three kidney sections from three rats of each group were immunohistochemically stained and were subjected to ImageJ analysis. For each parameter, means which share the same superscript letter(s) are not significantly different.
Biomolecules 10 01317 g020
Biomolecules 10 01317 g021 550
Figure 21. Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on relative kidney NF-κB p65 expression detected by Western blot in ethylene glycol-administered rats. Means which share the same letter(s) are not significantly different.
Figure 21. Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on relative kidney NF-κB p65 expression detected by Western blot in ethylene glycol-administered rats. Means which share the same letter(s) are not significantly different.
Biomolecules 10 01317 g021
Biomolecules 10 01317 g022 550
Figure 22. Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on relative kidney NF-κB p50 expression detected by Western blot in ethylene glycol-administered rats. Means which share the same letter(s) are not significantly different.
Figure 22. Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on relative kidney NF-κB p50 expression detected by Western blot in ethylene glycol-administered rats. Means which share the same letter(s) are not significantly different.
Biomolecules 10 01317 g022
Biomolecules 10 01317 g023 550
Figure 23. Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on relative kidney Bax expression detected by Western blot in ethylene glycol-administered rats. Means which share the same letter(s) are not significantly different.
Figure 23. Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on relative kidney Bax expression detected by Western blot in ethylene glycol-administered rats. Means which share the same letter(s) are not significantly different.
Biomolecules 10 01317 g023
Biomolecules 10 01317 g024 550
Figure 24. Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on relative kidney Bak expression detected by Western blot in ethylene glycol-administered rats. Means which share the same letter(s) are not significantly different.
Figure 24. Effect of P. ostreatus and A. bisporus aqueous extracts and carvedilol on relative kidney Bak expression detected by Western blot in ethylene glycol-administered rats. Means which share the same letter(s) are not significantly different.
Biomolecules 10 01317 g024
Biomolecules 10 01317 g025 550
Figure 25. Schematic diagram showing the effects of P. ostreatus and A. bisporus extracts and carvedilol on NF-κB, p53 and Bcl-2 to suppress inflammation and apoptosis together with the effects on oxidative stress.
Figure 25. Schematic diagram showing the effects of P. ostreatus and A. bisporus extracts and carvedilol on NF-κB, p53 and Bcl-2 to suppress inflammation and apoptosis together with the effects on oxidative stress.
Biomolecules 10 01317 g025
Table
Table 1. Preliminary phytochemical screening of A. bisporus and P. ostreatus.
Table 1. Preliminary phytochemical screening of A. bisporus and P. ostreatus.
MushroomP. ostreatusA. bisporus
Test
1—Carbohydrates and/or glycosides (Molish test)+ve+ve
2—Alkaloids and/or basic nitrogenous substances
(a)
Dragendroff’s test
(b)
Mayer’s test
(c)
Wagner’s test
+ve+ve
+ve+ve
+ve+ve
3—Flavonoides
(a)
Amyl alcohol test
(b)
Sodium hydroxide test
+ve+ve
−ve−ve
4—Resins test+ve+ve
5—Tannins
(a)
Ferric chloride test
(b)
Hydrochloric acid test
−ve−ve
+ve+ve
6—Unsaturated sterols and/or triterpenes
(a)
Libermann-Burchard test
(b)
Salkowiski’s test
+ve+ve
+ve+ve
Table
Table 2. Chemical composition of P. ostreatus aqueous extract as detected by GC-MS analysis.
Table 2. Chemical composition of P. ostreatus aqueous extract as detected by GC-MS analysis.
NumberRetention Time (Minutes)Compound or Group
(From Central Library Search Report)		Area %
(≥0.5%)
11.87(S)-(+)-Isoleucinol23.0
22.05Diethylhydroxylamine3.6
32.133-(dimethylamino)-propanenitrile1.4
42.171-Methylcyclopropanemethanol1.0
52.23N-Butyl-formamide3.5
62.542-(ethylthio) tetrahydro 2H-Pyran4.0
72.72N-Hydroxy-N-methyl methenamine24.2
82.852-Ethyl-2-butenal9.4
93.224-Methyl- 2,4,6-cycloheptatrien-1-one6.4
103.292-Phenylethanal4.2
113.472-Pyrrolidinone4.4
123.793-Mercapto-1-propanol4.0
134.30N,N,N′-Trimethyl-1,3-propanediamine3.4
144.542,5-Dihydro-3-methyl-furan1.2
154.722,3-Dimethyl-pentanal1.2
165.01N,N-Diethyl-N′, N′-dimethyl-1,2-ethanediamine3.6
176.264-Amino-1,2,5-Oxadiazole-3-carbonitrile0.5
1810.46Thiomorpholine0.5
1911.112,3′-Dipyridyl0.5
Table
Table 3. Chemical composition of A. bisporus aqueous extract as detected by GC-MS analysis.
Table 3. Chemical composition of A. bisporus aqueous extract as detected by GC-MS analysis.
NumberRetention TimeCompound or Group
(From Central Library Search Report)		Area %
(≥0.5%)
12.69N-Methoxymethanamine30.6
23.19Phenyl oxirane5.8
33.272-Phenylethanal2.6
43.442-Pyrrolidinone7.9
53.782-Propenylidene cyclobutene3.0
64.311-Methoxy-3-methyl- benzene2.4
75.013-Pentanone2.1
85.40N-[4-Aminobutyl]aziridine1.7
917.33N-Methoxy-methanamine4.2
1025.882,4,6,7,8,8a-Hexahydro-3,8-dimethyl-4-(1-methylethylidene)-(8S-cis)-5(1H)-azulenone3.2
1130.456-Ethyl-2,3-dihydro-2,7-dimethyl-5-oxo-5H-oxazolo[3,2-a]pyridine-8-carbonitrile13.7
1231.41Oxime, (5. alpha.) androstan-3-one6.5
1331.926-Amino-2-Phenazinol2.1
1432.99Fumaric acid, 2-heptyl octyl ester13.1

Share and Cite

MDPI and ACS Style

Ahmed, O.M.; Ebaid, H.; El-Nahass, E.-S.; Ragab, M.; Alhazza, I.M. Nephroprotective Effect of Pleurotus ostreatus and Agaricus bisporus Extracts and Carvedilol on Ethylene Glycol-Induced Urolithiasis: Roles of NF-κB, p53, Bcl-2, Bax and Bak. Biomolecules 2020, 10, 1317. https://doi.org/10.3390/biom10091317

AMA Style

Ahmed OM, Ebaid H, El-Nahass E-S, Ragab M, Alhazza IM. Nephroprotective Effect of Pleurotus ostreatus and Agaricus bisporus Extracts and Carvedilol on Ethylene Glycol-Induced Urolithiasis: Roles of NF-κB, p53, Bcl-2, Bax and Bak. Biomolecules. 2020; 10(9):1317. https://doi.org/10.3390/biom10091317

Chicago/Turabian Style

Ahmed, Osama M., Hossam Ebaid, El-Shaymaa El-Nahass, Mahmoud Ragab, and Ibrahim M. Alhazza. 2020. "Nephroprotective Effect of Pleurotus ostreatus and Agaricus bisporus Extracts and Carvedilol on Ethylene Glycol-Induced Urolithiasis: Roles of NF-κB, p53, Bcl-2, Bax and Bak" Biomolecules 10, no. 9: 1317. https://doi.org/10.3390/biom10091317

APA Style

Ahmed, O. M., Ebaid, H., El-Nahass, E.-S., Ragab, M., & Alhazza, I. M. (2020). Nephroprotective Effect of Pleurotus ostreatus and Agaricus bisporus Extracts and Carvedilol on Ethylene Glycol-Induced Urolithiasis: Roles of NF-κB, p53, Bcl-2, Bax and Bak. Biomolecules, 10(9), 1317. https://doi.org/10.3390/biom10091317

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop