Brassica juncea L. (Mustard) Extract Silver NanoParticles and Knocking off Oxidative Stress, ProInflammatory Cytokine and Reverse DNA Genotoxicity

Detoxification is one of the main vital tasks performed by the liver. The purpose of this study was to investigate whether mustard in its normal or nanoparticles could confer a protective/therapeutic effect against TAA-induced acute liver failure in experimental animal models. Mustard ethanolic extract was analyzed by HPLC/MS. To induce liver failure, male rats were injected with 350 mg/kg bw TAA IP, then treated orally with a dose of 100 mg/kg for 15 d of mustard extract and its nanoform before and following induction. The levels of serum liver functions, total cholesterol (TCHo), total glyceride (TG), total bilirubin (TBIL), hepatic malonaldhyde (MDA) and nitric oxide (NO),glutathione (GSH), sodium oxide dismutase (SOD), as well as tumor necrosis factor (TNF-α,) and interleukin 6 (IL-6), were estimated. DNA genotoxicity and hepatic pathology, and immunohistologic (IHC) changes were assayed. The antioxidant content of Phenolic acids, flavonoids in mustard ethanolic extract substantially decreased the levels of ALT, AST, ALP and rehabilitated the histopathological alterations. In addition, nanoforms of mustard ethanol extract have notably increased the levels of GSH, SOD and significantly reduced the levels of MDA. The expression levels of TNF-α and IL-6 in serum and tissue were markedly downregulated. DNA genotoxicity was significantly reversed. Mustard introduced a protective and medicinal effect against TAA in both its forms.


Introduction
The liver is one of the most important organs responsible for the process of metabolism and selective uptake and clearance of drugs xenobiotic and environmental toxins, the matter which makes it very sensitive to drug toxicity [1]. Thioacetamide C2H5NS/TAA is an organosulfur compound known to induce acute or chronic liver disease (fibrosis and cirrhosis) in the experimental animal model very similar to that happen in humans. TAA toxicity results from a series of biotransformation into toxic metabolites that takes place in cytochrome P-450 enzymes in the liver [2]. analytical grade solvent of/MeOH, filtered using a membrane disc filter (0.2 µm), then subjected to LC-ESI-MS analysis. Samples injection volumes (10 µL) were injected into the UPLC instrument equipped with reverse phase C-18 column (ACQUITY UPLC-BEH C18 1.7 µm particle size-2.1 × 50 mm Column). Sample mobile phase was prepared by filtering using 0.2 µm filter membrane disc and degassed by sonication before injection. Mobile phase elution was made with the flow rate of 0.2 mL/min using mobile gradient phase comprising two eluents: eluent A is H 2 O acidified with 0.1% formic acid, and eluent B is MeOH acidified with 0.1% formic acid. Elution was performed using the above gradient. The parameters for analysis were carried out using negative ion mode as follows: source temperature 150 • C, cone voltage 30 eV, capillary voltage 3 kV, desolvation temperature 440 • C, cone gas flow 50 L/h, and desolvation gas flow 900 L/h. Mass spectra scanning was detected in the ESI negative ion mode between m/z 100-1000. The peaks and spectra were processed using the MassLynx 4.1 software and tentatively identified by comparing its retention time (R t ) and mass spectrum with reported data [13][14][15].

Synthesis of Mustard Silver Nanoparticles
B. juncea/mustard seed extract was used to synthesize (mustard-AgNPs). According to Hassan et al. [16], silver nitrate (0.017 g) was added in 100 mL of double distilled water to prepare 1 mM silver nitrate solution. Then, 1 mL of ethanolic mustard extract was added to 50 mL of silver nitrate (1 mM) solution and incubated for 24 h in a dark chamber to minimize photo-activation of silver nitrate at room temperature under static conditions for nucleation of the silver nanoparticles. The reduction of elemental Ag to AgO was confirmed by the color change from colorless to brownish-yellow, indicating that ethanolic mustard extract was encapsulated into the silver nanoparticles in the form of pellets. The suspensions were subjected to centrifugation for the pellets to settle, which were then dried using a vacuum dryer.

Characterization of Synthesized Silver Nanoparticles
UV-vis spectral analysis was done by using Shimadzu visible spectrophotometer (UV-1800, Japan). The periodic scans of the optical absorbance between 300 and 700 nm with a double-beam UV-visible spectrophotometer (Carry 100 with tungsten halogen light sources) were performed at room temperature to investigate the reduction of silver ions by seed extract.
Field emission scanning electron microscopy (FESEM), the morphology, particle dispersion, and chemical composition of the prepared Nanostructures were investigated by (FESEM) (Quanta 450) equipped with EDS at accelerating voltage 30 kV and further confirmed by transmission electron microscopy (TEM) for internal surface morphology using a JEOL JEM 1200 transmission electron microscope (JEOL Ltd., Peabody, MA, USA) [17].

Animals
A total of 64Westar rats weighing 180-200 g were taken from the breeding laboratory of the National Research Center and kept in an animal care facility. Rats were held in reserve in polypropylene cages at room temperature with a 12 h light-dark cycle and relative humidity of 60% ± 1%. Animals were provided purified water ad libitum with standard laboratory rat chow. The study was approved by the animal ethics committee of the Institutional Review Board of National Research Center [No 20061]. The animal protocol was designed to lessen pain or distress to the animals. TAA (Sigma-Aldrich Chemical, ST. Louis, MO, USA) was dissolved in physiological saline, and the appropriately selected dose of 350 mg/kg bw was injected intraperitoneal (i.p.) in 1 mL volume [3].

Experimental protocol
The rats were divided into 8 groups consisting of 8 rats each as follows: • Group (G 1): Normal healthy cont. (3% Tween-80) and water, respectively • Group (G 2): Intoxicated group was treated intraperitoneal (i.p.) with 350 mg/kg bw of freshly prepared TAA in a single shot [3], 5% glucose solution was added to the drinking water to avoid dehydration 24 h post-injection. • Groups (G3, G4): were given orally; the standard plant extract and its nano forms (NMs) in a dose of I mL [100 mg/kg] for two weeks as a benchmark/control group of plant extract [12].

•
Prophylactic groups (G5, G6): administered a dosage of 1 mL of standard mustard extract and/or its nanoform for two weeks prior to i.p. TAA insulting 350 mg/kg bw in one shot, by then continued with the same dosage of 1 mL of both extracts for two weeks. • Treatment groups (G7, G8): were given orally; the standard plant extract and its nanoforms in a dose of 1 mL as a treatment for two weeks after (i.p.) single injection with the same assigned dose of TAA. Twenty-four hours following the last drug administration, blood samples were withdrawn from the retro-orbital plexus of the rats under light ether anesthesia. Then, rats were sacrificed by cervical dislocation under the same anesthesia for the collection of liver samples. A weighed part of the liver of each animal was rapidly dissected out, washed and homogenized using phosphate-buffered saline (PBS, 50 mM potassium phosphate, pH 7.5) at 4 • C to produce a 20% homogenate. Liver homogenates were kept at −80 • C until analysis. Another part of liver tissue was kept in 10% formalin-saline for histopathological and immunohistopathological examinations.

Histopathological Studies
A division of the liver was preserved in 10% buffer formalin for at least 24 h. and then embedded in paraffin according to the standard protocol. Sections were cut into 5 µm-thick portions, transferred onto glass slides, and stained with hematoxylin and eosin (HE), investigated microscopically for any histopathological and immunohistochemical changes as well [24] Histopathological and Immunohistochemical Examinations Five micrometer-thick sections of paraffinized liver stained with hematoxylin and eosin were examined histopathologically under Zeiss microscope (Carl Zeiss Microscopy GmbH 07,745 Jena, Germany) with ×200, ×400 magnification powers. For immunohistochemical examinations of IL6, TNF α were performed on liver sections cuts from the paraffin blocks with a commercially available anti-mouse IL6, TNF α antibodies (Santa Cruz Biotechnology, CA, USA) at the optimal working dilution of 1:100. Briefly, slides were sectioned at 4 µm onto positively charged slides (Super frost plus, Menzel-Glaser, Germany), and the slides were stained on an automated platform (Dako Autostainer Biomolecules 2020, 10, 1650 5 of 19 Link 48). Heat-induced antigen retrieval was used for 30 min at 97 • C in the high-PH Envision™ FLEX Target Retrieval Solution, and the primary antibody was used at a dilution of 1 in 100. The percent of positively stained brown cytoplasm (IL6, TNF α) were examined in 10 microscopic fields (under Zeiss light microscopy at ×400).

Statistical Analysis
Statistical analysis of all data was expressed as mean ± SD of 8 rats in each group by using one-way analysis of variance (ANOVA), the CoStat software computer program accompanied with least significance difference (LSD) between groups at a significant level at p < 0.05. The percentage of improvement in both the prophylactic group and the treatment one was calculated according to the equation.

Results
The current results revealed that the incubation of 50 mL of 1 mM AgNO 3 with 1 mL of mustard extract for 24 h at "room temperature" led to the synthesis of AgNPs as indicated by the development of the brown color. The spectrophotometric analysis showed a maximum absorption picture of the developed brown color at 425 nm ( Figure 1).

The Visual Observation of Color Changes of Silver Nano Mustard (B. juncea) Extract
Biomolecules 2020, 10, x 5 of 18 Autostainer Link 48). Heat-induced antigen retrieval was used for 30 min at 97 °C in the high-PH Envision™ FLEX Target Retrieval Solution, and the primary antibody was used at a dilution of 1 in 100.The percent of positively stained brown cytoplasm (IL6, TNF α) were examined in 10 microscopic fields (under Zeiss light microscopy at x400).

Statistical Analysis
Statistical analysis of all data was expressed as mean ± SD of 8 rats in each group by using oneway analysis of variance (ANOVA), the CoStat software computer program accompanied with least significance difference (LSD) between groups at a significant level at p < 0.05.The percentage of improvement in both the prophylactic group and the treatment one was calculated according to the equation.

Results
The current results revealed that the incubation of 50 mL of 1 mM AgNO3 with 1 mL of mustard extract for 24 h at "room temperature" led to the synthesis of AgNPs as indicated by the development of the brown color. The spectrophotometric analysis showed a maximum absorption picture of the developed brown color at 425 nm ( Figure 1).

The Visual Observation of Color Changes of Silver Nano Mustard (B. juncea) Extract
LC/MS results tentatively manifested twenty-eight phenolic compounds in the ethanolic extract of mustard. (Table 1, Figure 3). Fourteen phenolic acids and its glycosides were detected and determined as follow compounds 1, 2, 3, 4 and 5 were eluted at retention time (Rt) 13.

Effect of Brassica juncea L. (Mustard) Extract and Its Nanoforms on Liver Functions
The examination of ALT, AST and ALP are given in (Table 2). Single injections of TAA (350 mg/kg bw) significantly elevated the serum activities of ALT, AST and ALP by 2.3, 2.7 and 1.9-fold respectively at P <0.0001 compared to the normal control group. Administration of ethanolic extraction of B. Juncea at doses of 100 mg/kg bw was a prophylactic and/or treatment substantially dwindled the elevation of transaminases with different percentages of improvement, which are represented in Table 2. Table 2. Restorative and prophylactic impacts of Brassica juncea L. (mustard) extract in its normal and its nanostructure on liver function parameters. Data are mean ± SD of 8 rats in each group. Statistical analysis was done using one-way analysis of variance (ANOVA) using the CoStat computer program accompanied by the least significant level (LSD) between groups at p < 0.05. Unshared superscript letters are significant values between groups at p < 0.0001. Table 3 shows that experimental groups treated with TAA demonstrated a significant increase in the serum levels of total cholesterol (TC), triglycerides (TG), total lipids (TP), total bilirubin (TBIL) as compared with the healthy control group at (p < 0.05). Pretreatment with 100 mg/kg bw of B. juncea plant extract before and after intoxication with TAA and post-treatment with the same dose both resulted in a decrease of the above-mentioned parameters with mean levels differing from the normal and TAA groups at (p < 0.0001). However, the largest percentage of improvement change was achieved by nano plant extract rather than the remaining treatment classes. Data are mean ± SD of 8 rats in each group. Statistical analysis was done using one-way analysis of variance (ANOVA) using the CoStat computer program accompanied by the least significant level (LSD) between groups at p < 0.05. Unshared superscript letters with significant values between groups at p < 0.0001.

Effect of Brassica juncea L. (Mustard) Extract in Their Normal and Its Nanoforms on Oxidative Stress Markers and Inflammatory Cytokines
A substantial decrease in the superoxide dismutase and glutathione levels in the challenged group following TAA injury p (p < 0.0001). However, pre-and post-treatment with B. juncea extract could improve the deterioration in the antioxidant parameters compared to the control group. Groups treated with mustard extract and its nano form exhibited the best improvement percentage rather than the pretreatment groups. In contrast with oxidative parameters, which showed an increase in each lipid peroxidation and nitric oxide levels in the challenged TAA intoxicated group at p < 0.0001 ( Table 4). The treatment with Mustard extract (B. juncea) and its nanoforms showed a prominent reduction in oxidative parameters either as a prophylactic or as a treatment with different percentages of improvement (Table 4). The TAA-intoxication resulted in a remarkable elevation at (p < 0.05) in the measured inflammatory markers IL6 and TNFα by a 2.5-fold increase compared to the control group (Table 4). While B. Juncea extracts substantially reversed IL6 and TNFα levels in both preand post-treatment classes. In most antioxidant parameters as well as in inflammatory markers, the treatment with nanoform (TNMs) of B. juncea obtained the most amelioration outcomes. Data are represented as mean ± SD of 8 rats in each group. One-way analysis of variance (ANOVA) was employed using the CoStat computer program accompanied by the least significant level (LSD) between groups at p < 0.05. Unshared superscript letters are significant values between groups at p < 0.0001.

Effects of Brassica juncea L. (mustard) Extract and Its Nanoparticles on DNA Degradation
Fragmentation of DNA was assessed using the comet assay. Compared to the normal control group, TAA has substantially caused DNA damage. This DNA damage was demonstrated significantly in terms of an increase in the comet parameters presented as tail length with different three classes ( Figure 4A,B), tail and tail moment DNA (percentage); the primary predictive parameter for DNA damage (Table 5). In the hepatotoxic community, there was a large broom-like tail and a small comet eye ( Figure 4A), a typical component of toxic DNA damage and apoptosis. The length of the tail increases as DNA damage increases, as seen in (Figure 4A,B). In the meantime, administration of Mustard (B. juncea) both in its natural or in its nano pretreatment has counterbalanced the TAA effect as demonstrated by a considerable reduction in the length of the tail; this changed into extra glaring in the mustard nano form (Table 5). Data are represented as mean ± SD of 8 rats in each group. One-way analysis of variance (ANOVA) was employed using the CoStat computer program accompanied by the least significant level (LSD) between groups at p < 0.05. Unshared superscript letters are significant values between groups at p <0.0001.

Effects of Brassica juncea L. (mustard) Extract and its Nanoparticles on DNA Degradation
Fragmentation of DNA was assessed using the comet assay. Compared to the normal control group, TAA has substantially caused DNA damage. This DNA damage was demonstrated significantly in terms of an increase in the comet parameters presented as tail length with different three classes ( Figure 4A,B), tail and tail moment DNA (percentage); the primary predictive parameter for DNA damage (Table 5).In the hepatotoxic community, there was a large broom-like tail and a small comet eye ( Figure 4A), a typical component of toxic DNA damage and apoptosis. The length of the tail increases as DNA damage increases, as seen in (Figure 4A,B). In the meantime, administration of Mustard (B. juncea) both in its natural or in its nano pretreatment has counterbalanced the TAA effect as demonstrated by a considerable reduction in the length of the tail; this changed into extra glaring in the mustard nano form (Table 5).

Hematoxylin and Eosin Pathological Examination
Liver sections of normal rats showed normal cellular architectures, normal morphology, hepatocyte and central vein ( Figure 5A). The TAA-intoxicated group displayed partial distortion of hepatic lobular architecture, with moderate hydropic degeneration of hepatocytes and binucleated hepatocytes accompanied by vein congestion with thick fibrous tissue in the portal tract ( Figure 5B). Mustard (B. juncea) treatment (100 mg/kg) pre-post either in normal or nanoforms has shown observable healing effect presented, as shown in (Figure 5C-H).
Liver sections of normal rats showed normal cellular architectures, normal morphology, hepatocyte and central vein ( Figure 5A). The TAA-intoxicated group displayed partial distortion of hepatic lobular architecture, with moderate hydropic degeneration of hepatocytes and binucleated hepatocytes accompanied by vein congestion with thick fibrous tissue in the portal tract ( Figure 5B). Mustard (B. juncea) treatment (100 mg/kg) pre-post either in normal or nanoforms has shown observable healing effect presented, as shown in (Figure 5C-H).  showed severe abnormalities, partial distortion of lobular hepatic architecture (black arrow), with moderate hydropic degeneration of hepatocyte (red arrow) and thick fibrous tissue in portal tract (blue arrow); (C,D) liver sections treated with MS and nano MS showed hepatic tissue with almost normal intact hepatic lobular architecture and structure, hepatocytes arranged in thin plates (black arrow) and sinusoids (yellow arrow), central vein (red arrow), binucleated nuclei (green arrow); (E,F) liver sections treated orally with PMS nano PMS as a prophylactic group. They demonstrated tangible improvement as hepatic tissue was almost in normal intact hepatic lobular architecture and structure; hepatocytes arranged in thin plates (black arrow) with mild interlobular inflammatory infiltration (green arrow) and sinusoids (yellow arrow), congested central vein (red arrow), hepatocytes with moderate hydropic degeneration (white arrow); (G,H) liver sections treated with MS and MS nano groups showed improvement in hepatic tissues as it appeared in intact lobular hepatic architecture, hepatocyte with thin plates (black arrow), congested central vein (red arrow) and congested sinusoids (yellow arrow) ((H,E), ×400).

Impact of Mustard Extract and Its Nanoform on the Inflammatory Markers through Immunohistochemistry
The anti-inflammatory effect of Mustard extract and its nano form was further evaluated via follow-up of the expression of IL-6 ( Figure 6) and TNF-α (Figure 7) in hepatic tissues immunohistochemically. TAA intoxication 350 mg/kg bw resulted in a substantial elevation in TNF-α and IL-6 expression that were located mostly in the cytoplasm of hepatocytes in portal tract and fibrous septa compared to normal control group A, B. However, treatment with Mustard extract and its nanoforms either pre or after TAA intoxication improved and downregulated the expression of both TNF-α and IL6 Figures 6 and 7 from (C-H), respectively, with the notion indicated that nano mustard extract has more potential to inhibit the inflammatory response induced by TAA intoxication.
follow-up of the expression of IL-6 ( Figure 6) and TNF-α (Figure 7) in hepatic tissues immunohistochemically. TAA intoxication 350 mg/kg bw resulted in a substantial elevation in TNFα and IL-6 expression that were located mostly in the cytoplasm of hepatocytes in portal tract and fibrous septa compared to normal control group A, B. However, treatment with Mustard extract and its nanoforms either pre or after TAA intoxication improved and downregulated the expression of both TNF-α and IL6 Figures 6 and 7 from (C-H), respectively, with the notion indicated that nano mustard extract has more potential to inhibit the inflammatory response induced by TAA intoxication.

Discussion
In the current study, green chemistry was employed to synthesize AgNPs using mustard seed extract (MSE).The change in the color of AgNO3 after 24 h incubation with (MSE) in the dark pointed to the ability of the extract of (MSE) to reduce AgNO3 to AgNPs. This result has been observed previously and indicated that the change in color might be appeared due to the surface plasmon resonance of the deposited AgNPs [25,26]. Formation of AgNPs was confirmed by the SEM and TEM as they ensured that the synthesized nanoparticles were within the nanoscale size 4.8-40 nm. Mustard is an ancient plant known since Biblical times; subsequent scientific and

Discussion
In the current study, green chemistry was employed to synthesize AgNPs using mustard seed extract (MSE). The change in the color of AgNO 3 after 24 h incubation with (MSE) in the dark pointed to the ability of the extract of (MSE) to reduce AgNO 3 to AgNPs. This result has been observed previously and indicated that the change in color might be appeared due to the surface plasmon resonance of the deposited AgNPs [25,26]. Formation of AgNPs was confirmed by the SEM and TEM as they ensured that the synthesized nanoparticles were within the nanoscale size 4.8-40 nm. Mustard is an ancient plant known since Biblical times; subsequent scientific and pharmacological studies verified its antimicrobial, analgesic, anti-inflammatory, antipyretic, antidiabetic and hepatoprotective qualities [2,27]. Perhaps and to the best of our knowledge, no more published data about the impact of mustard in acute liver failure.
The present results revealed through the LC/MS analysis that mustard (B. juncea L.) seeds extract (MSE) is rich in phenolic acids and flavonoid compounds, kaempferols glycosides, fatty acids. Many studies indicated that phenolic and flavonoids compounds are directly contributed to the antioxidant activities [28]. These antioxidant properties of the plant phenolic compounds are primarily due to the redox properties of these compounds, which enable them to donate hydrogen, act as singlet oxygen quenchers and reducing agents, as mentioned previously [29].
Serum liver enzymes are biomarkers to monitor and display the injure and aids in the clinical diagnosis of liver toxicity conditions [30]. When there is an injury to the liver due to any cause, then these enzymes are spilled into the blood move. This was in complete agreement with our results, represented by a pronounced increase in the liver enzymes AST, ALT, and ALP in the serum as a response to TAA injection. A leakage was coupled with a loss of liver architecture, hydropic degeneration, central vein obstruction and hepatic lymphocytes infiltration (Table 1, Figure 5). As thioacetamide is a potent centrilobular hepatotoxicant, its effects have been extended to increase cholesterol, glyceride, total lipid, total bilirubin levels indicating oxidative damage of the liver (Table 3). However, a substantive improvement and reduction in these parameters were observed after remedy with B. juncea in its both forms either as a prophylactic or as a treatment; however, the nanoforms have shown a greater significant effect on the elevated serum liver enzymes and the rehabilitation of the liver architecture as well. These outcomes go in line with Yang et al. [31] and seem to be consistent with what recently announced by Khaled [32], Melrose [27] and Le et al. [33] as they archived the amazing cell reinforcement and hepatoprotective properties of mustard against poisonousness instigated free radicals harm in the liver and furthermore with Walia et al. [11] as he detailed ethanolic leaf concentrate of B. juncea could be a superior medication of decision as a hepatoprotective plant source. The free radicals scavenging effects of mustard extracts are most in all likelihood attributed to its better polyphenols and flavones contents.
It is worth noting that the antioxidant impact of polyphenols is mainly due to their redox properties, which allow them to behave as reducing agents, hydrogen donors, singlet oxygen quenchers, metal chelators [34,35]. Moreover, our findings showed a marked decrease with a sensible percentage of improvements in the levels of cholesterol, total glycerides, total lipids and total bilirubin when treated with mustard extract in its normal and in its nanoform either pre-or post-TAA administration. Result consequences can be interpreted on the basis of the phytocomponents structure of mustard seeds extract to have the potential to act in a synergistic way to lessen hyperlipidemia and hypercholesterolemia and go with full coincidence with Lee et al. [36] when they used B. juncea L. leaf extract on fat deposition and lipid profiles. The current observations suggest B. juncea L. seeds be clinically functional for treating dyslipidemia, although the mechanisms underlying still needed to be investigated.
In another hand bile, acid synthesis plays a major role in hepatic regulation of cholesterol homeostasis as well as in the catabolism of cholesterol bilirubin is considered a physiologically important antioxidant [37], with beneficial effects at mildly elevated concentrations, and can neutralize ROS and prevent oxidative damage [38][39][40]. These results may also provide an explanation for the increment of total bilirubin as a justification mechanism of the body against TAA free radicals. Interestingly mustard extract in its two forms, either pre-or post-treatment dose, showed a significant improvement in bilirubin level. That improvement was pronounced with the nano mustard treatment formula to be in concurrence with Rawat et al. [41].
As unquestionably demonstrated, oxidative stress and inflammation are the two essential players driving forces behind various diseases. This was confirmed by the significant decrease in GSH and SOD levels along with the elevation in MDA, serum NO together with the marked disturbances in TNF-α and IL6 levels ( Table 4). These outcomes may confirm the hepatotoxic TAA and its capability to cause hepatic damage and act as an initiator for a series of serious inflammatory changes via ROS generation and antioxidant protection mechanism regulation [42,43].
It is well established that plant extracts with antioxidant potential can protect against the oxidative damage caused by TAA hepatotoxicity [2]. The present study confirmed this observation and demonstrated that mustard extract and its nanoform substantially increased the levels of GSH and SOD, whether pre-or post-TAA injection. Our findings may be in full settlement with Keshari et al. [44] as they reported that stimulation of the Nrf2/ARE pathway is essential for antioxidant defense enzyme induction and intracellular GSH modulation in response to stress. Consequently, mustard can play an antioxidant role in acute liver damage. Interestingly, mustard extract and its nano remodulated the level of lipid peroxide, restoring it back to near normal. It additionally decreased the overproduction of NO, which is commonly linked to the lack of cytochrome P450 content and injury in rat hepatocytes [45].
Moreover, a marked increase in serum levels of TNF-α and IL6 pro-inflammatory markers had been recorded in the challenged TAA group in both serum and tissue in comparison to the control results (Table 4 and Figure 6). It can clearly be seen the expression of TNF-αandIL6 is about 70%. These findings may ensure that the entire inflammatory cascade, including the activation of transcription factors, is activated when the redox status is attached [46][47][48]. However, these parameters were remodulated and downregulated by mustard extract treatment in both normal and its nano form either pre-or post TAA intoxication. These good responses may be supportive of Le et al. [33] as they suggested the anti-inflammatory properties of the B. juncea spice/herb ( Figure 6).
From a near perspective, data from this research showed that thioacetamide could interact with DNA and induce changes in the hepatic cells ( Figure 4). While TAA/challenged group damage DNA was demonstrated by an increase in the tail moment. However, B. juncea therapy. Ethanolic extract in normal or nanoform decreased DNA damage dramatically and reversed the comet's length back to normal. These findings can be interpreted on the basis of the antioxidant phytochemical components contained in the mustard extract, which carry a high flavonoid diffusion rate into the membranes, allowing them to scavenge oxy radicals in the lipid bilayer at several sites. The results may be in harmony with the results of Zargar et al. [49], as he used rutin before two weeks of TAA assault and resulted in the complete reversal of TAA-mediated hepatic toxicity. Our results also go in the same connection with Ansar et al. [50], who proposed that flavonoids may also be involved in the indirect induction of detoxifying genes, which may promote detoxification of TAA and decrease its toxicity.
It is noteworthy that this study was designed to investigate the mustard extract in its natural or in its nano sort either as a prophylactic or as a treatment against the insult of TAA inducing acute liver failure. We would like to draw to the reader's attention that treatment with mustard nano form has shown superiority over the ethanol normal extract formula. The matter which reflects the efficiency of the nanoparticles in term of their existence of the essential functional groups to make AgNPs very stable and prevent it from being anchored. In addition, the existence of the bioactive molecules on the surface of AgNPs may increase its efficacy and bioavailability. It can also enhance its solubility, improve plasma half-life, preventing degradation in the intestinal environment and increasing permeation in the small intestine, which may confer strong antioxidative activity [51,52]. Although the results of the present study support mustard as a great candidate for liver, It appears that mustard and its nanoparticles may initiate comets, Table 5. Mustard in both forms cannot efficiently switch/ reverse the DNA fragmentations back or close to the normal. This result may be credited to a few leftover pesticides within the mustard seed itself or may predict some toxic components contained within the mustard. Azubuike et al. [12]. Duy and Trang [53] recorded that B. juncea seeds contain saponins, flavonoids and tannins. In expansion, mustard oil is well known to contain glycerides of erucic acid, which is considered harmful to human wellbeing. Hence, these observations recommend that drawn-out utilization of B. juncea seed extract may have some hepatotoxic impacts. The matter which motivates more extensive research in order to explore the behind plausible mechanism.

Conclusions
Our experimental findings demonstrated that the plant under investigation (mustard) possesses a potent antioxidative-inflammatory effect, and its nanostructure is more potent than its typical. The LC/MS Phytochemical analysis of the plant extract demonstrates the presence of a plethora of powerful compounds like phenolic and flavonoids compounds, which brought possible mechanism of hepatoprotective activity due to their free radical scavenging and antioxidant properties in addition to their anti-inflammatory effects. These properties are mediated by downregulating the liver function enzymes, lipid profile, oxidative stress, expression of TNF-α, and IL-6. in both serum and tissue. Although we acknowledge these results as not only has it been revealed that the ethanolic concentration of Brassica juncea L. has a reasonable measure of safety and risks, the study also provided new insights into the possible role of mustard in the treatment of acute liver injury. Funding: This study was thankfully supported by the "Researchers Supporting Project", King Saud University, Riyadh, Saudi Arabia. through the grant number RSP/2020/45.