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Article

Effects of Chronic Thermal Stress on Performance, Energy Metabolism, Antioxidant Activity, Brain Serotonin, and Blood Biochemical Indices of Broiler Chickens

by
Omar A. Ahmed-Farid
1,
Ayman S. Salah
2,
Mohamed Abdo Nassan
3 and
Mahmoud S. El-Tarabany
4,*
1
Physiology Department, National Organization for Drug Control and Research (NODCAR), Giza 35521, Egypt
2
Department of Animal Nutrition and Clinical Nutrition, Faculty of Veterinary Medicine, New Valley University, El-Kharga 72511, Egypt
3
Department of Clinical Laboratory Sciences, Turabah University College, Taif University, Taif 21944, Saudi Arabia
4
Department of Animal Wealth Development, Faculty of Veterinary Medicine, Zagazig University, Zagazig 44511, Egypt
*
Author to whom correspondence should be addressed.
Animals 2021, 11(9), 2554; https://doi.org/10.3390/ani11092554
Submission received: 3 June 2021 / Revised: 23 June 2021 / Accepted: 23 June 2021 / Published: 31 August 2021
(This article belongs to the Special Issue Oxidative Stress in Animal/Poultry Production: Molecular Mechanisms and Protection)
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Abstract

:

Simple Summary

In the tropical and subtropical regions, heat stress is the main limiting factor of poultry industries. In this context, broilers are more liable to thermal stress due to their fast growth, rapid metabolic rate, and high level of production. The aim of the current work was to analyze changes in the brain serotonin, energy metabolism, antioxidant biomarkers, and blood chemistry of broiler chickens subjected to chronic thermal stress. Thermal stress disturbed the antioxidant defense system and energy metabolism and exhausted ATP levels in the liver tissues of broiler chickens. Interestingly, chronic thermal stress reduced the level of brain serotonin and the activity of CoQ10 in liver tissues.

Abstract

The aim of this paper was to investigate the effects of chronic thermal stress on the performance, energy metabolism, liver CoQ10, brain serotonin, and blood parameters of broiler chickens. In total, 100 one-day-old chicks were divided into two equal groups of five replicates. At 22 days of age and thereafter, the first group (TN) was maintained at a thermoneutral condition (23 ± 1 °C), while the second group (TS) was subjected to 8 h of thermal stress (34 °C). The heat-stressed group showed significantly lower ADFI but higher FCR than the thermoneutral group (p = 0.030 and 0.041, respectively). The TS group showed significantly higher serum cholesterol, ALT, and AST (p = 0.033, 0.024, and 0.010, respectively). Meanwhile, the TS group showed lower serum total proteins, albumin, globulin, and Na+ than the TN group (p = 0.001, 0.025, 0.032, and 0.002, respectively). Furthermore, the TS group showed significantly lower SOD and catalase in heart tissues (p = 0.005 and 0.001, respectively). The TS group showed significantly lower liver ATP than the TN group (p = 0.005). Meanwhile, chronic thermal stress significantly increased the levels of ADP and AMP in the liver tissues of broiler chickens (p = 0.004 and 0.029, respectively). The TS group showed significantly lower brain serotonin (p = 0.004) and liver CoQ10 (p = 0.001) than the TN group. It could be concluded that thermal stress disturbed the antioxidant defense system and energy metabolism and exhausted ATP levels in the liver tissues of broiler chickens. Interestingly, chronic thermal stress reduced the level of brain serotonin and the activity of CoQ10 in liver tissues.

1. Introduction

For decades, thermal stress has been considered the main limiting factor of the poultry industry in tropical and subtropical regions [1]. Indeed, increased global warming will exaggerate heat stress-related problems [2]. When housing temperatures surpass comfort level, birds try to minimize metabolic heat production through a reduction in feed consumption [3], which consequently reduces growth rate and profitability [4]. In this context, broiler chickens are more susceptible to thermal stress due to their high growth rate and related high metabolic heat production [5].
Several parameters are traditionally measured as thermal stress biomarkers in broiler chickens, including plasma concentrations of corticosterone, cholesterol, protein fractions, electrolytes, and antioxidants [6]. Furthermore, thermal stress adversely affects cellular organelles, impairing oxidative metabolism and the functional structures of membranes [7]. Thermal stress also increases plasma cholesterol, reduces serum proteins, activates the lipid peroxidation process in blood and tissues, and disturbs electrolyte balance in the body [8]. Indeed, heat stress can increase the production of ROS in mitochondria and, consequently, reduce energy generation efficiency and adenosine triphosphate (ATP) synthesis [9]. Mujahid et al. [10] also stated that mitochondria are more susceptible to oxidative damage, probably due to the high percentage of polyunsaturated fatty acids and proteins in their membranes. Harmful heavy metal cadmium can cause mitochondrial damage and oxidative stress in common carp (Cyprinus carpio L.) gills [11]. Additionally, the toxic gas ammonia can damage mitochondria, affect energy metabolism, and lead to oxidative stress in the chicken thymus [12]. Coenzyme Q (CoQ) acts as an electron carrier and has been considered a major oil-soluble antioxidant within cellular membranes and other lipophilic structures. Furthermore, its antioxidant properties include the inhibition of the oxidative process of lipids and proteins, as well as the regeneration of other antioxidants such as vitamin E [9]. Meanwhile, studies on the bioavailability of CoQ under thermal stress conditions are relatively limited.
Serotonin (5-HT) is an important signaling molecule involved in several neurotransmitter functions of the brain. Outside the brain, serotonin plays a key role in regulating the contractility of the gastrointestinal smooth muscle and epithelial secretions [13]. In vertebrates, serotonin is stored in the enterochromaffin cells. These cells are numerous in the mucosal epithelium of the gastrointestinal tract [14]. Furthermore, it is believed that serotonin regulates the process of bone formation, as well as the mechanism of bone resorption [15]. In this context, Calefi et al. [16] reported that acute stress conditions such as environmental temperature increases the concentration of serotonin in brain tissues; however, chronic stress conditions decrease the level of brain serotonin. Therefore, the aim of the current work is to analyze changes in the brain serotonin, liver CoQ10, energy metabolism, antioxidant biomarkers, and blood chemistry of broiler chickens subjected to chronic thermal stress.

2. Materials and Methods

2.1. Birds and Management

In total, 100 one-day-old chicks (Ross) were divided into 2 equal groups of five replicates (10 birds/replicate). Housing pens were provided with fresh wood shavings (15 birds/m2), and birds had free access to feed and water. Regular supplementation of heat was performed by digital heaters to maintain a stable housing temperature (automated diesel heater; Naganpuriya High Tech Farming Equipment). Both groups were housed at 34 °C during the first week of age. Thereafter, the temperature was reduced gradually to reach 23 °C at 21 days of age. The first group (TN) was maintained at a thermoneutral condition (23 ± 1 °C), while the other group (TS) was subjected to 8 h of heat stress at 34 °C (08:00–16:00 and 23 ± 1 °C for the remaining time). The relative humidity was adjusted to 58 ± 3%, and regular observation was practiced to check the stability of the housing temperature and ventilation. Furthermore, the mortality rate was recorded in both experimental groups. A routine vaccination program against Newcastle disease and Gumboro disease was applied. All birds fed the same starter and grower–finisher diets [17] (see Table 1). Body weight and feed intake were recorded weekly to determine the average daily feed intake (ADFI) and feed conversion ratio (FCR) during the period of 22–42 days of age.

2.2. Blood Sampling and Biochemical Analyses

At 42 days of age, 3 mL blood samples were collected in plain tubes (10 birds/group). The serum samples were separated (1200× g) and stored at −20 °C. The concentrations of serum cholesterol, AST, ALT, total protein, and albumin were determined by Roch diagnostics kits (GmbH, Mannheim, Germany). The activity of total antioxidant capacity (TAC) in the serum samples was measured (Cell Biolabs kits, Inc., San Diego, CA, USA). The levels of serum sodium (Na) and potassium (K) were estimated by an electrolyte analyzer (Shenzhen Kindle Medical Devices Co. Ltd., Shenzhen, China).

2.3. Determination of Brain Serotonin

At 42 days of age, two birds from each replicate (10 birds/group) were fasted for 6 h and slaughtered according to the Islamic method (HALAL Slaughter) of the Malaysian institutes [18]. The main jugulars of broiler chickens are severed with sharp knives without using any anesthetics to get effective bleeding. Brain samples (striatum, frontal cortex, and hypothalamus) were homogenized in HPLC-grade methanol solution [19]. After the derivatization process was completed, the dried samples were mixed with a diluent composed of 0.71 g of disodium hydrogen phosphate (pH of 7.4) plus 5% acetonitrile. The homogenate of each sample was run at (4000 rpm) for 10 min, and the supernatant was collected. The level of brain serotonin was determined by HPLC in accordance with the method described by Pagel et al. [20]. Compared with the standard, the resulting chromatogram had to characterize the concentration of serotonin as μg per gram of brain tissue.

2.4. Determination of Antioxidant Activity in Heart Tissues

Five heart samples were obtained from each group. Each homogenate heart sample was prepared in a 10 mM phosphate buffer (pH 7.4). Then, the suspension was centrifuged at 12,000× g for 10 min at 4 °C to collect the clear supernatant. The activities of superoxide dismutase (SOD) and catalase (CAT) in the supernatant were determined according to the method described by Ahmed-Farid et al. [21]. The SOD activity was observed at two-minute intervals. The activity was illustrated as the amount of enzyme that inhibits the autoxidation of pyrogallol. Based on the decomposition of H2O2, the CAT activity was measured [22].

2.5. Determination of CoQ10 and Energy Biomarkers in Liver Tissues

Liver adenosine contents of tri-, di-, and monophosphate (ATP, ADP, and AMP) were quantified by HPLC in accordance with the protocol described by Teerlink et al. [23]. The serum samples were prepared by mixing 0.2 mL of serum with 0.3 mL of methanol (70%), then centrifuged (5000 rpm) at 4 °C for 20 min to obtain the supernatant. Fifty hundred microliters of liver tissue were homogenized with ice-cold 10% potassium chloride, then centrifuged at 5000 rpm for 20 min to collect the clear supernatant. For deprotonization, 200 µL of supernatant was mixed with 1 mL of methanol (70%) and prepared for HPLC analysis (Nova-PakTM C18 column). The reports and chromatograms were obtained from the ChemStation program, with a wavelength of 254 nm and an injection volume of 20 µL. Liver CoQ10 contents were quantified by HPLC (Agilent HP 1200 series apparatus, Santa Clara, CA, USA) according to the modified protocol of Niklowitz et al. [24].

2.6. Statistical Analysis

The data were analyzed using ANOVA procedures in the IBM SPSS software program (Version 16.0; IBM Corp., New York, NY, USA). For performance traits, each pen was considered an experimental unit. The model included the fixed effects of the thermal treatment (two levels: TN and TS) and the random effect of experimental error. Body weight at 21 days of age was included as a covariate in the statistical model. The outputs are expressed as means and the standard error of means (SEM). The results are considered significant at level p ˂ 0.05.

3. Results

As described in Figure 1, the heat-stressed group showed significantly lower ADFI but higher FCR than the thermoneutral group (p = 0.030 and 0.041, respectively).
The effects of chronic thermal stress on the blood chemistry of broiler chicken are illustrated in Table 2. The TS group showed significantly higher serum cholesterol, ALT, and AST than the TN group (p = 0.033, 0.024, and 0.010, respectively). Meanwhile, the TS group showed significantly lower serum total proteins, albumin, globulin, and Na+ (p = 0.001, 0.025, 0.032, and 0.002, respectively). The levels of serum K+ and A/G ratio did not differ between experimental groups (p = 0.603 and 0.239, respectively).
The effects of chronic thermal stress on the antioxidant activity of broiler chickens are illustrated in Table 3. Thermal stress significantly decreased serum TAC in broilers compared with broilers maintained at thermoneutral conditions (p = 0.021). Furthermore, the TS group showed significantly lower SOD and catalase in heart tissues (p = 0.005 and 0.001, respectively).
The effects of thermal stress on energy biomarkers in liver tissues are illustrated in Table 4. The TS group showed significantly lower liver ATP than the TN group (p = 0.005). Meanwhile, chronic thermal stress significantly increased the levels of ADP and AMP in the liver tissues of broiler chickens (p = 0.004 and 0.029, respectively). The level of liver Na,K-ATPase did not differ between experimental groups (p = 0.115).
The TS group showed significantly lower brain serotonin (p = 0.004) and liver CoQ10 (p = 0.001) than the TN group (Figure 2).

4. Discussion

Adverse environmental conditions such as ambient temperature may cause significant economic losses to the poultry industry due to their negative effects on performance indices. In this context, broiler chickens are more susceptible to stress conditions, probably due to their rapid growth rate [25]. The majority of the literature, however, has focused on acute or short-duration thermal stresses. Herein, chronic thermal stress conditions reduced feed intake and increased the FCR in broiler chickens. Consistent with our findings, Roushdy et al. [7] stated that chronic thermal stress (daily, 6 h at 34 °C, for three consecutive weeks) deteriorates the FCR in both Ross and Cobb broiler chickens. During the late fattening period, Quinteiro-Filho et al. [4] also reported a significant reduction in body gain and an increase in the FCR when broilers were exposed to 36 °C for 10 h daily. The adverse effects of thermal stress on broiler performance may be attributed to the quick synthesis and release of cortisol in the adrenal cortex. Additionally, stress conditions may impair intestinal integrity, causing an inability to absorb nutrients [26,27]. Unsurprisingly, the reduced feed consumption in the TS group is consistent with previous studies [28,29,30]. Attia and Hassan [31] supposed that thermal stress stimulates the peripheral thermal receptors of broiler chickens to transmit inhibitory nerve impulses to the appetite center in the hypothalamus and, consequently, reduce feed consumption. Others suggested that brain monoamines, including serotonin, are involved in the control of feed intake [32]; hence, stress conditions may activate the central monoaminergic system [33]. Additionally, serotonin is an essential messenger to modulate the brain–gut connection, as well as the maintenance of gastrointestinal motility and visceral sensation [34]. In this context, the lower concentration of brain serotonin in the heat-stressed group may explain the reduction in feed intake in broiler chickens.
Blood biochemical indexes can indicate the metabolic and physiological responses of broiler chickens to different nutritional and environmental conditions [35]. In the current study, the TS group showed higher concentrations of serum ALT and AST. This may indicate some sort of hepatic damage in heat-stressed broilers [36]. Consistent with these findings, Zhang et al. [37] reported that exposure to thermal stress (34 ± 1 °C for 8 h) increases the activities of serum AST and ALT. Moreover, Lan et al. [38] reported that high ambient temperature induces liver damage and increases serum AST and ALT. Herein, chronic thermal stress deteriorated the indices of serum proteins, as well as increased the level of serum cholesterol. Similarly, Attia et al. [39] reported a significant increase in serum cholesterol when broilers were subjected to prolonged thermal stress (36 °C). Others recorded similar cholesterol findings when birds were exposed to cyclic thermal stress conditions [40]. Thermal stress disturbs the electrolyte balance in broiler chickens. Consistent with these findings, Zaglool et al. [41] reported that serum Na+ was significantly reduced when broiler chickens were subjected to 6 h of thermal stress. This electrolyte disturbance may be attributed to increased water consumption and the related hemodilution process [42], or to the loss of body water due to decreased extracellular fluids [43].
Thermal stress accelerates the lipid peroxidation process and, consequently, exhausts the antioxidant defense system in broiler chickens [44]. The current study also demonstrated a significant reduction in the level of serum TAC of heat-stressed broilers. Xue et al. [45] recorded a great depletion in serum antioxidant activity when Arbor Acres broiler chickens were exposed to cyclic thermal stress. Under thermal stress conditions, the expected exhaustion of the antioxidant defense system in broiler chickens may be due to the rapid oxidation process and related cellular damages [46]. It is believed that both catalase and SOD act as the first line of the antioxidant defense system in the body tissues. Herein, chronic thermal stress reduced the levels of SOD and catalase in the heart tissues of broiler chickens. Consistent with these findings, Zeng et al. [47] reported that the activities of SOD and catalase were significantly decreased in liver tissues when Pekin ducks were subjected to short-term heat stress (p < 0.05).
The accumulation of ROS in mitochondria is associated with thermal stress, as well as with subsequent damage to proteins, lipids, and DNA structures. When thermal stress is prolonged, mitochondrial homeostasis is disturbed, and ATP synthesis is decreased [9]. In the present study, chronic thermal stress reduced the concentration of ATP in liver tissues. Additionally, the increased liver ADP in heat-stressed broilers indicates the impaired energy metabolism of birds. In this context, Joung et al. [48] suggested that stress-induced depletion of ATP in liver tissues induces necrosis patterns with more severe liver injuries. Of note, it is believed that short-term stress disturbs the activity of Na+,K+-ATPase in broiler chickens [49]. In the current study, chronic thermal stress did not exert significant changes in the activity of Na+,K+-ATPase in liver tissues. However, Chen et al. [50] demonstrated that acute heat stress significantly reduced Na+-K+-ATPase in the intestinal mucosa of chickens. Coenzyme Q10 is a naturally occurring lipophilic compound that regulates the process of oxidative phosphorylation in mitochondria and acts as an antioxidant [51]. It is also involved in the synthesis of ATP and regulation of the bioenergetics pathway [52]. In the current trial, chronic thermal stress reduced the activity of CoQ10 in the liver tissues of broiler chickens. In this context, Xu et al. [53] reported that CoQ10 reduces oxidative damage to chicken myocardial cells.
Serotonin is a neurotransmitter involved in different neurological functions of the brain and nervous system. It is also an important messenger in the digestive tract and in the regulation of gastrointestinal motility and visceral sensation [34]. In the current study, the heat-stressed group showed significantly lower brain serotonin than the thermoneutral group. In this context, the reduced FI in the heat-stressed group may be attributed to fluctuating serotonin levels. Supporting this explanation, Raybould [13] suggested that serotonin plays a crucial role in controlling the contractility of smooth muscle in the GIT, as well as the activity of secretory epithelial cells. Consistent with our findings, Buraczewska et al. [54] stated that the addition of crystalline tryptophan to broiler diets increased the concentration of serotonin in brain tissues, with a significant increase in feed consumption. On the contrary, Denbow et al. [55] reported that tryptophan supplements increased the level of brain serotonin in turkeys but had no effect on feed intake.

5. Conclusions

It could be concluded that chronic thermal stress reduces the performance, serum proteins, and TAC, as well as the activity of SOD and catalase in the heart tissues of broiler chickens. Furthermore, chronic thermal stress disturbs energy metabolism by exhausting ATP levels in the liver tissues of broilers. Interestingly, chronic thermal stress reduced the level of brain serotonin and activity of CoQ10 in the liver tissues in broiler chickens. The present results may be helpful to target appropriate strategies to minimize the adverse effects of thermal stress in broiler chickens.

Author Contributions

Conceptualization, O.A.A.-F., A.S.S. and M.S.E.-T.; methodology, O.A.A.-F., A.S.S. and M.S.E.-T.; formal analysis, O.A.A.-F., A.S.S. and M.S.E.-T.; investigation, O.A.A.-F., A.S.S. and M.S.E.-T.; resources, O.A.A.-F., A.S.S., M.S.E.-T. and M.A.N.; data curation, O.A.A.-F., A.S.S. and M.S.E.-T.; writing—original draft preparation, O.A.A.-F., A.S.S., M.S.E.-T. and M.A.N.; writing—review and editing, A.S.S. and M.S.E.-T.; visualization, O.A.A.-F., A.S.S., M.S.E.-T. and M.A.N.; supervision, O.A.A.-F., A.S.S. and M.S.E.-T. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki, and approved by the Animal Ethics Committee of Zagazig University, Egypt (Approval No. ZU-IACUC/2/F/93/2021).

Data Availability Statement

Data sharing is not applicable. All data analyzed during this study are included in this published paper.

Acknowledgments

The authors would like to acknowledge and to thank the Taif University Researchers Supporting Project number (TURSP-2020/71), Taif University, Taif, Saudi Arabia.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Lin, H.; Jiao, H.C.; Buyse, J.; Decuypere, E. Strategies for preventing heat stress in poultry. World’s Poult. Sci. J. 2006, 62, 71–85. [Google Scholar] [CrossRef]
  2. Hansen, J.; Ruedy, R.; Sato, M.; Lo, K. Global surface temperature change. Rev. Geophys. 2010, 48. [Google Scholar] [CrossRef] [Green Version]
  3. Swennen, Q.; Verhulst, P.-J.; Collin, A.; Bordas, A.; Verbeke, K.; Vansant, G.; Decuypere, E.; Buyse, J. Further investigations on the role of dietinduced thermogenesis in the regulation of feed intake in chickens: Comparison of adult cockerels E62 Bottje and Carstens of lines selected for high or low residual feed intake. Poult. Sci. 2007, 86, 1960–1971. [Google Scholar] [CrossRef]
  4. Quinteiro-Filho, W.M.; Ribeiro, A.; Ferraz-de-Paula, V.; Pinheiro, M.L.; Sakai, M.; Sá, L.R.M.; Ferreira, A.J.P.; Palermo-Neto, J. Heat stress impairs performance parameters, induces intestinal injury, and decreases macrophage activity in broiler chickens. Poult. Sci. 2010, 89, 1905–1914. [Google Scholar] [CrossRef] [PubMed]
  5. Gous, R.M. Nutritional limitations on growth and development in poultry. Livest. Sci. 2010, 130, 25–32. [Google Scholar] [CrossRef]
  6. El-Tarabany, M.S. Effect of thermal stress on fertility and egg quality of Japanese quail. J. Therm. Biol. 2016, 61, 38–43. [Google Scholar] [CrossRef]
  7. Roushdy, E.M.; Zaglool, A.W.; El-Tarabany, M.S. Effects of chronic thermal stress on growth performance, carcass traits, antioxidant indices and the expression of HSP70, growth hormone and superoxide dismutase genes in two broiler strains. J. Therm. Biol. 2018, 74, 337–343. [Google Scholar] [CrossRef]
  8. Akbarian, A.; Golian, A.; Kermanshahi, H.; De Smet, S.; Michiels, J. Antioxidant enzyme activities, plasma hormone levels and serum metabolites of finishing broiler chickens reared under high ambient temperature and fed lemon and orange peel extracts and C urcuma xanthorrhiza essential oil. J. Anim. Physiol. Anim. Nutr. 2015, 99, 150–162. [Google Scholar] [CrossRef] [PubMed]
  9. Akbarian, A.; Michiels, J.; Degroote, J.; Majdeddin, M.; Golian, A.; De Smet, S. Association between heat stress and oxidative stress in poultry; mitochondrial dysfunction and dietary interventions with phytochemicals. J. Anim. Sci. Biotechnol. 2016, 7, 37. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  10. Mujahid, A.; Pumford, N.R.; Bottje, W.; Nakagawa, K.; Miyazawa, T.; Akiba, Y.; Toyomizu, M. Mitochondrial oxidative damage in chicken skeletal muscle induced by acute heat stress. J. Poult. Sci. 2007, 44, 439–445. [Google Scholar] [CrossRef] [Green Version]
  11. Chen, J.; Chen, D.; Li, J.; Liu, Y.; Gu, X.; Teng, X. Cadmium-induced oxidative stress and immunosuppression mediated mitochondrial apoptosis via JNK-FoxO3a-PUMA pathway in common carp (Cyprinus carpio L.) gills. Aquat. Toxicol. 2021, 233, 105775. [Google Scholar] [CrossRef]
  12. Shah, S.W.A.; Chen, D.; Zhang, J.; Liu, Y.; Ishfaq, M.; Tang, Y.; Teng, X. The effect of ammonia exposure on energy metabolism and mitochondrial dynamic proteins in chicken thymus: Through oxidative stress, apoptosis, and autophagy. Ecotoxicol. Environ. Saf. 2020, 206, 111413. [Google Scholar] [CrossRef]
  13. Raybould, H.E. Visceral perception: Sensory transduction in visceral afferents and nutrients. Gut 2002, 51 (Suppl. 1), i11–i14. [Google Scholar] [CrossRef]
  14. Fink, C.; Tatar, M.; Failing, K.; Hospes, R.; Kressin, M.; Klisch, K. Serotonin-Containing cells in the gastrointestinal tract of newborn foals and adult horses. Anat. Hist. Embryol. 2006, 35, 23–27. [Google Scholar] [CrossRef]
  15. Ducy, P. 5-HT and bone biology. Curr. Opin. Pharmacol. 2011, 11, 34–38. [Google Scholar] [CrossRef]
  16. Calefi, A.S.; Fonseca, J.G.D.S.; Nunes, C.A.Q.; Lima, A.P.N.; Quinteiro-Filho, W.M.; Flório, J.C.; Zager, A.; Ferreira, A.J.P.; Palermo-Neto, J. Heat stress modulates brain monoamines and their metabolites production in broiler chickens co-infected with Clostridium perfringens type A and Eimeria spp. Vet. Sci. 2019, 6, 4. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  17. NRC. Nutrient Requirements of Poultry, 9th ed.; National Academy Press: Washington, DC, USA, 1994. [Google Scholar]
  18. JAKIM (Department of Islamic Development Malaysia). Malaysian Protocol for the Halal Meat and Poultry Productions; JAKIM: Putrajaya, Malaysia, 2011; pp. 1–30. [Google Scholar]
  19. Arafa, N.M.S.; Salem, S.M.A.; Farid, O.A.H.A. Influence of echinacea extract pre- or postnatal supplementation on immune and oxidative status of growing rabbits. Ital. J. Anim. Sci. 2010, 9, 338–343. [Google Scholar]
  20. Pagel, P.; Blome, J.; Wolf, H.U. High-performance liquid chromatographic separation and measurement of various biogenic compounds possibly involved in the pathomechanism of Parkinson’s disease. J. Chromatogr. B 2000, 746, 297–304. [Google Scholar] [CrossRef]
  21. Ahmed-Farid, O.A.; Nasr, M.; Ahmed, R.F.; Bakeer, R.M. Beneficial effects of Curcumin nano-emulsion on spermatogenesis and reproductive performance in male rats under protein deficient diet model: Enhancement of sperm motility, conservancy of testicular tissue integrity, cell energy and seminal plasma amino acids content. J. Biomed. Sci. 2017, 24, 66. [Google Scholar]
  22. Aebi, H. Catalase in vitro. Methods Enzymol. 1984, 105, 121–126. [Google Scholar] [PubMed]
  23. Teerlink, T.; Hennekes, M.; Bussemaker, J.; Groeneveld, J. Simultaneous determination of creatine compounds and adenine nucleotides in myocardial tissue by high-performance liquid chromatography. Anal. Biochem. 1993, 214, 278–283. [Google Scholar] [CrossRef]
  24. Niklowitz, P.; Doring, F.; Paulussen, M.; Menke, T. Determination of coenzyme Q10 tissue status viahigh-performance liquid chromatography with electrochemical detection in swine tissues (Sus scrofa domestica). Anal. Biochem. 2013, 437, 88–94. [Google Scholar] [CrossRef]
  25. Geraert, P.A.; Guillaumin, S.; Leclercq, B. Are genetically lean broilers more resistant to hot climate? Br. Poult. Sci. 1993, 34, 643–653. [Google Scholar] [CrossRef]
  26. Alhenaky, A.; Abdelqader, A.; Abuajamieh, M.; Al Fataftah, A.R. The effect of heat stress on intestinal integrity and Salmonella invasion in broiler birds. J. Therm. Biol. 2017, 70, 9–14. [Google Scholar] [CrossRef]
  27. Bayraktar, B.; Tekce, E.; Aksakal, V.; Gül, M.; Takma, C.; Bayraktar, S.; Bayraktar, F.G.; Eser, G. Effect of the addition of essential fatty acid mixture to the drinking water of the heat stress broilers on adipokine (Apelin, BDNF) response, histopathologic findings in liver and intestines, and some blood parameters. Ital. J. Anim. Sci. 2020, 19, 656–666. [Google Scholar] [CrossRef]
  28. Olfati, A.; Mojtahedin, A.; Sadeghi, T.; Akbari, M.; MartínezPastor, F. Comparison of growth performance and immune responses of broiler chicks Reared under heat stress, Cold stress and thermoneutral conditions. Span. J. Agric. Res. 2018, 16, e0505. [Google Scholar] [CrossRef] [Green Version]
  29. Goo, D.; Kim, J.H.; Park, G.; Reyes, J.; Kil, D. Effect of heat stress and Stocking Density on growth performance, Breast meat quality, and intestinal barrier function in broiler chickens. Animals 2019, 9, 107. [Google Scholar] [CrossRef] [Green Version]
  30. Awad, E.A.; Najaa, M.; Zulaikha, Z.A.; Zulkifli, I.; Soleimani, A.F. Effects of heat stress on growth performance, selected physiological and immunological parameters, caecal microflora, and meat quality in two broiler strains. Asian Australas J. Anim. Sci. 2020, 33, 778–787. [Google Scholar] [CrossRef] [PubMed]
  31. Attia, Y.A.; Hassan, S.S. Broiler tolerance to heat stress at various dietary protein/energy levels. Eur. Poult. Sci. 2017, 81. [Google Scholar] [CrossRef]
  32. Orosco, M.; Nicolaidis, S. Spontaneous feeding-related monoaminergic changes in the rostromedial hypothala-mus revealed by microdialysis. Physiol. Behav. 1992, 52, 1015–1019. [Google Scholar] [CrossRef]
  33. Chauloff, F. Physiopharmacological interactions between stress hormones and central serotonergic systems. Brain Res. Rev. 1993, 18, 1–32. [Google Scholar] [CrossRef]
  34. Delesalle, C.; van de Walle, G.R.; Nolten, C.; Donck, L.V.; Hemelrijck, A.; Drinkenburg, W.; Bosschere, H.; Claes, P.; Deprez, P.; Lefère, L.; et al. Determination of the source of increased serotonin (5-HT) concentrations in blood and peritoneal fluid of colic horses with compromised bowel. Equine Vet. J. 2008, 40, 326–331. [Google Scholar] [CrossRef] [PubMed]
  35. Zhu, X.; Liu, W.; Yuan, S.; Chen, H. The effect of different dietary levels of thyme essential oil on serum biochemical indices in Mahua broiler chickens. Ital. J. Anim. Sci. 2014, 13, 576–581. [Google Scholar] [CrossRef] [Green Version]
  36. Polat, U.; Yesilbag, D.; Eren, M. Serum biochemical profile of broiler chickens fed diets containing rosemary and rosemary volatile oil. J. Biol. Environ. Sci. 2011, 5, 29–30. [Google Scholar]
  37. Zhang, J.; Bai, K.W.; He, J.; Niu, Y.; Lu, Y.; Zhang, L.; Wang, T. Curcumin attenuates hepatic mitochondrial dysfunction through the maintenance of thiol pool, inhibition of mtDNA damage, and stimulation of the mitochondrial thioredoxin system in heat-stressed broilers. J. Anim. Sci. 2018, 96, 867–879. [Google Scholar] [CrossRef] [Green Version]
  38. Lan, R.; Wei, L.; Chang, Q.; Wu, S.; Zhihui, Z. Effects of dietary chitosan oligosaccharides on oxidative stress and inflammation response in liver and spleen of yellow-feather broilers exposed to high ambient temperature. Ital. J. Anim. Sci. 2020, 19, 1508–1517. [Google Scholar] [CrossRef]
  39. Attia, Y.A.; Al-Harthi, M.A.; El-Shafey, A.S.; Rehab, Y.A.; Kim, W.K. Enhancing tolerance of broiler chickens to heat stress by supplementation with vitamin E, vitamin C and/or probiotics. Ann. Anim. Sci. 2017, 17, 1155–1169. [Google Scholar] [CrossRef] [Green Version]
  40. Rodrigues Bueno, J.P.; Bueno de Mattos Nascimento, M.R.; Machado da Silva Martins, J.; Ferreira Prazeres Marchini, C.; Ruggeri Menezes Gotardo, L.; Miranda Ribeiro de Sousa, G.; Mundim, A.V.; Carvalho Guimarães, E.; Pereira Rinaldi, F. Effect of age and cyclical heat stress on the serum biochemical profile of broiler chickens. Semin. Ciências Agrárias 2017, 38, 1383–1392. [Google Scholar] [CrossRef] [Green Version]
  41. Zaglool, A.W.; Roushdy, E.M.; El-Tarabany, M.S. Impact of strain and duration of thermal stress on carcass yield, metabolic hormones, immunological indices and the expression of HSP90 and Myogenin genes in broilers. Res. Vet. Sci. 2019, 122, 193–199. [Google Scholar] [CrossRef]
  42. Borges, S.; Fischer da Silva, A.; Majorka, A.; Hooge, D.; Cummings, K. Physiological responses of broiler chickens to heat stress and dietary electrolyte balance (sodium plus potassium minus chloride, milliequivalents per kilogram). Poult. Sci. 2004, 83, 1551–1558. [Google Scholar] [CrossRef] [PubMed]
  43. Olanrewaju, H.A.; Thaxton, J.P.; Dozier, W.A.; Branton, S.L. Electrolyte diets, stress, and acid-base balance in broiler chickens. Poult. Sci. 2007, 86, 1363–1371. [Google Scholar] [CrossRef] [PubMed]
  44. Azad, M.A.; Kikusato, M.; Maekawa, T.; Shirakawa, H.; Toyomizu, M. Metabolic characteristics and oxidative damage to skeletal muscle in broiler chickens exposed to chronic heat stress. Comp. Biochem. Physiol. A Mol. Integr. Physiol. 2010, 155, 401–406. [Google Scholar] [CrossRef] [PubMed]
  45. Xue, B.; Song, J.; Liu, L.; Luo, J.; Tian, G.; Yang, Y. Effect of epigallocatechin gallate on growth performance and antioxidant capacity in heat-stressed broilers. Arch. Anim. Nutr. 2017, 71, 362–372. [Google Scholar] [CrossRef]
  46. Zhang, Z.Y.; Jia, G.Q.; Zuo, J.J.; Zhang, Y.; Lei, J.; Ren, L.; Feng, D.Y. Effects of constant and cyclic heat stress on muscle metabolism and meat quality of broiler breast fillet and thigh meat. Poult. Sci. 2012, 91, 2931–2937. [Google Scholar] [CrossRef]
  47. Zeng, T.; Li, J.J.; Wang, D.Q.; Li, G.Q.; Wang, G.L.; Lu, L.Z. Effects of heat stress on antioxidant defense system, inflammatory injury, and heat shock proteins of Muscovy and Pekin ducks: Evidence for differential thermal sensitivities. Cell Stress Chaperones 2014, 19, 895–901. [Google Scholar] [CrossRef]
  48. Joung, J.Y.; Cho, J.H.; Kim, Y.H.; Choi, S.H.; Son, C.G. A literature review for the mechanisms of stress-induced liver injury. Brain Behav. 2019, 9, e01235. [Google Scholar] [CrossRef]
  49. Chen, C.L.; Sangiah, S.; Chen, H.; Roder, J.D.; Shen, Y. Effects of heat stress on Na+, K+-ATPase, Mg2+-activated ATPase, and Na+-ATPase activities of broiler chickens vital organs. J. Toxicol. Environ. Health Part A 1994, 41, 345–356. [Google Scholar] [CrossRef]
  50. Chen, Z.; Xie, J.; Wang, B.; Tang, J. Effect of gammaaminobutyric acid on digestive enzymes, absorption function, and immune function of intestinal mucosa in heatstressed chicken. Poult. Sci. 2014, 93, 2490–2500. [Google Scholar] [CrossRef] [PubMed]
  51. Gopi, M.; Purushothaman, M.R.; Chandrasekaran, D. Effect of dietary coenzyme Q10 supplementation on the growth rate, carcass characters and cost effectiveness of broiler fed with three energy levels. SpringerPlus 2014, 3, 518. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  52. Geng, A.L.; Guo, Y.M.; Yang, Y. Reduction of ascites mortality in broilers by coenzyme Q10. Poult. Sci. 2004, 83, 1587–1593. [Google Scholar] [CrossRef]
  53. Xu, J.; Tang, S.; Yin, B.; Sun, J.R.; Song, E.B.; Bao, E.D. Co-enzyme Q10 and Acetyl salicylic acid enhance Hsp70 expression in primary chicken myocardial cells to protect the cells during heat stress. Mol. Cell. Biochem. 2017, 435, 73–86. [Google Scholar] [CrossRef] [PubMed]
  54. Buraczewska, L.; Nguyen, C.V.; Mieczkowska, A. Effects of acidifier added to diets containing graded levels of crystalline tryptophan on growth performance, protein digestibility, and on brain. J. Anim. Feed Sci. 2004, 13, 289–300. [Google Scholar]
  55. Denbow, D.M.; Hobbs, F.C.; Hulet, R.M.; Graham, P.P.; Potter, L.M. Supplemental dietary L-tryptophan effects on growth, meat quality, and brain catecholamine and indolamine concentrations in turkeys. Br. Poult. Sci. 1993, 34, 715–724. [Google Scholar] [CrossRef] [PubMed]
Animals 11 02554 g001 550
Figure 1. Effects of chronic thermal stress on average daily feed intake (ADFI) and feed conversion ratio (FCR) of broiler chickens (p = 0.030 and 0.041, respectively). TN: Thermoneutral group; TS: Thermal-stressed group. a,b Values with different superscripts differ significantly.
Figure 1. Effects of chronic thermal stress on average daily feed intake (ADFI) and feed conversion ratio (FCR) of broiler chickens (p = 0.030 and 0.041, respectively). TN: Thermoneutral group; TS: Thermal-stressed group. a,b Values with different superscripts differ significantly.
Animals 11 02554 g001
Animals 11 02554 g002 550
Figure 2. Effects of chronic thermal stress on brain serotonin and liver CoQ10 of broiler chickens (p = 0.004 and 0.001, respectively). TN: Thermoneutral group; TS: Thermal-stressed group. a,b Values with different superscripts differ significantly.
Figure 2. Effects of chronic thermal stress on brain serotonin and liver CoQ10 of broiler chickens (p = 0.004 and 0.001, respectively). TN: Thermoneutral group; TS: Thermal-stressed group. a,b Values with different superscripts differ significantly.
Animals 11 02554 g002
Table
Table 1. Ingredient composition and calculated chemical analysis of the basal diets.
Table 1. Ingredient composition and calculated chemical analysis of the basal diets.
IngredientsStarter Period (1–21 d, g kg−1)Grower–Finisher Period (22–42 d, g kg−1)
Yellow maize605.0650.0
Soybean meal (48%)308.0250.0
Corn gluten (60%)40.035.0
Maize oil-18.0
Di-calcium phosphate23.023.0
Limestone14.014.0
DL-methionine1.01.0
Lysine1.01.0
Vitamin and trace mineral mix3.53.5
Salt (NaCl)3.53.5
Coccidostate1.01.0
Calculated analysis
1 ME (KJ/kg)1234212949
Crude protein224.0197.5
Calcium10.510.5
Available phosphorus4.54.5
Lysine11.811.4
Methionine4.84.5
1 ME: metabolizable energy.
Table
Table 2. Effect of chronic thermal stress on blood chemistry of broiler chickens.
Table 2. Effect of chronic thermal stress on blood chemistry of broiler chickens.
ParameterExperimental Groups
TN 1TS 2SEM 3p-Value
Total protein (g/dL)6.635.860.140.001
Albumin (g/dL)4.384.070.070.025
Globulin (g/dL)2.251.790.110.032
Albumin/Globulin ratio2.012.320.130.239
Cholesterol (mg/dL)79.3384.951.370.033
4 ALT (U/L)54.9660.601.310.024
5 AST (U/L)44.4053.351.910.010
K+ (mmol/L)4.043.940.080.603
Na+ (mmol/L)133.4113.93.690.002
1 Thermoneutral group; 2 thermal-stressed group; 3 standard error of means; 4 alanine aminotransferase; 5 aspartate aminotransferase.
Table
Table 3. Effect of chronic thermal stress on antioxidant activity of broiler chickens.
Table 3. Effect of chronic thermal stress on antioxidant activity of broiler chickens.
ParameterExperimental Groups
TN 1TS 2SEM 3p-Value
4 SOD (U/g, heart)43.2035.211.600.005
5 Catalase (U/g, heart)12.789.220.570.001
5 TAC (U/L, serum)1.511.380.030.021
1 Thermoneutral group; 2 thermal-stressed group; 3 standard error of means; 4 superoxide dismutase; 5 total antioxidant capacity.
Table
Table 4. Effect of chronic thermal stress on energy biomarkers in liver tissues of broiler chickens.
Table 4. Effect of chronic thermal stress on energy biomarkers in liver tissues of broiler chickens.
ParameterExperimental Groups
TN 1TS 2SEM 3p-Value
4 ATP (μg/g)36.8630.151.340.005
5 ADP (μg/g)22.6326.110.680.004
6 AMP (μg/g)9.3710.380.250.029
Na,K-ATPase (μmol/g)469.9515.213.50.115
1 Thermoneutral group; 2 thermal-stressed group; 3 standard error of means; 4 adenosine triphosphate; 5 adenosine diphosphate; 6 adenosine monophosphate.
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Ahmed-Farid, O.A.; Salah, A.S.; Nassan, M.A.; El-Tarabany, M.S. Effects of Chronic Thermal Stress on Performance, Energy Metabolism, Antioxidant Activity, Brain Serotonin, and Blood Biochemical Indices of Broiler Chickens. Animals 2021, 11, 2554. https://doi.org/10.3390/ani11092554

AMA Style

Ahmed-Farid OA, Salah AS, Nassan MA, El-Tarabany MS. Effects of Chronic Thermal Stress on Performance, Energy Metabolism, Antioxidant Activity, Brain Serotonin, and Blood Biochemical Indices of Broiler Chickens. Animals. 2021; 11(9):2554. https://doi.org/10.3390/ani11092554

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Ahmed-Farid, Omar A., Ayman S. Salah, Mohamed Abdo Nassan, and Mahmoud S. El-Tarabany. 2021. "Effects of Chronic Thermal Stress on Performance, Energy Metabolism, Antioxidant Activity, Brain Serotonin, and Blood Biochemical Indices of Broiler Chickens" Animals 11, no. 9: 2554. https://doi.org/10.3390/ani11092554

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