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Effect of in ovo feeding of γ-aminobutyric acid combined with embryonic thermal manipulation on hatchability, growth, and hepatic gene expression in broilers

  • Chris Major, Ncho (Department of Animal Science, Gyeongsang National University) ;
  • Akshat, Goel (Institute of Agriculture and Life Sciences, Gyeongsang National University) ;
  • Vaishali, Gupta (Division of Applied Life Sciences (BK21 Plus Program), Gyeongsang National University) ;
  • Chae-Mi, Jeong (Institute of Agriculture and Life Sciences, Gyeongsang National University) ;
  • Yang-Ho, Choi (Department of Animal Science, Gyeongsang National University)
  • Received : 2022.03.11
  • Accepted : 2022.06.07
  • Published : 2023.02.01

Abstract

Objective: This study investigated the effects of in ovo feeding of γ-aminobutyric acid (GABA) and embryonic thermal manipulation (ETM) on growth performance, organ indices, plasma biochemical parameters, hepatic antioxidant levels, and expression of lipid metabolism-related genes in broilers. Methods: Two hundred and fifty eggs were assigned to one of four treatments: control eggs incubated under standard conditions (CON); eggs that received an in ovo injection of 10% GABA on day 17.5 of incubation (G10); thermally manipulated eggs between days 10 and 18 of incubation at 39.6°C for 6 h daily (TM); and eggs that received both treatments during incubation (G10+TM). After 28 days of rearing, five birds per treatment were selected for blood and organ sampling. Results: No differences were found in hatchability or growth parameters among different treatment groups. Hepatic gene expression of catalase (CAT) and glutathione peroxidase 1 (GPx1) was upregulated (p = 0.046 and p = 0.006, respectively) in the G10+TM group, while that of nuclear factor erythroid 2-related factor 2 (NRF2) was upregulated (p = 0.039) in the G10 group. In addition, the relative gene expression of NADPH oxidase 1 (NOX1) was significantly lower (p = 0.007) in all treatment groups than that in the CON group. Hepatic fatty acid synthase (FAS) levels and average daily feed intake (ADFI) of last week showed a positive correlation (r = 0.50, p = 0.038). In contrast, the relative gene expression of the extracellular fatty acid-binding protein (EXFAB) and peroxisome proliferator-activated receptor-γ (PPAR-γ) were positively correlated (r = 0.48, p = 0.042 and r = 0.50, p = 0.031) with the overall ADFI of birds. Conclusion: Taken together, the results of this study suggest that the combination of in ovo feeding of GABA and ETM can enhance hepatic antioxidant function in broilers.

Keywords

Acknowledgement

The authors are thankful to the Korean Government Scholarship Program (KGSP) and the Brain Pool Program funded by the Ministry of Science and ICT through the National Research Foundation of Korea (2019H1D3A1A01071142).

References

  1. Surai PF. Antioxidant systems in poultry biology: superoxide dismutase. J Anim Res Nutr 2016;1:8.
  2. Goel A, Ncho CM, Choi YH. Regulation of gene expression in chickens by heat stress. J Anim Sci Biotechnol 2021;12:11. http://doi.org/10.1186/s40104-020-00523-5
  3. Surai PF, Kochish II, Kidd MT. Redox homeostasis in poultry: regulatory roles of NF-κB. Antioxidants 2021;10:186. https://doi.org/10.3390/antiox10020186
  4. Chueh CC, Lin LJ, Lin WC, et al. Antioxidant capacity of banana peel and its modulation of Nrf2-ARE associated gene expression in broiler chickens. Ital J Anim Sci 2019;18:1394-403. https://doi.org/10.1080/1828051x.2019.1667884
  5. Chelikani P, Fita I, Loewen PC. Diversity of structures and properties among catalases. Cell Mol Life Sci 2004;61:192-208. https://doi.org/10.1007/s00018-003-3206-5
  6. Ma Q. Role of nrf2 in oxidative stress and toxicity. Annu Rev Pharmacol Toxicol 2013;53:401-26. https://doi.org/10.1146/annurev-pharmtox-011112-140320
  7. Ncho CM, Jeong C, Gupta V, Goel A. The effect of gammaaminobutyric acid supplementation on growth performances, immune responses, and blood parameters of chickens reared under stressful environment: a meta-analysis. Environ Sci Pollut Res 2021;28:45019-28. https://doi.org/10.1007/s11356-021-13855-0
  8. Cobb SR, Buhl EH, Halasy K, Paulsen O, Somogyi P. Synchronization of neuronal activity in hippocampus by individual GABAergic interneurons. Nature 1995;378:75-8. https://doi.org/10.1038/378075a0
  9. El-Naggar K, El-Kassas S, Abdo SE, Kirrella AAK, Al Wakeel RA. Role of gamma-aminobutyric acid in regulating feed intake in commercial broilers reared under normal and heat stress conditions. J Therm Biol 2019;84:164-75. https://doi.org/10.1016/j.jtherbio.2019.07.004
  10. Hu H, Bai X, Shah AA, et al. Interactive effects of glutamine and gamma-aminobutyric acid on growth performance and skeletal muscle amino acid metabolism of 22-42-dayold broilers exposed to hot environment. Int J Biometeorol 2016;60:907-15. https://doi.org/10.1007/s00484-015-1084-9
  11. Choi YH. Effects of γ-aminobutyric acid on mortality in laying hens during summer time. J Agric Life Environ Sci 2019;53:131-9. https://doi.org/10.14397/jals.2019.53.2.131
  12. Ncho CM, Goel A, Jeong CM, Youssouf M, Choi YH. In ovo injection of gaba can help body weight gain at hatch, increase chick weight to egg weight ratio, and improve broiler heat resistance. Animals 2021;11:1364. https://doi.org/10.3390/ani11051364
  13. Ncho CM, Gupta V, Goel A. Effect of thermal conditioning on growth performance and thermotolerance in broilers: A systematic review and meta-analysis. J Therm Biol 2021;98:102916. https://doi.org/10.1016/j.jtherbio.2021.102916
  14. Al-Zghoul MB, Mohammad Saleh KM. Effects of thermal manipulation of eggs on the response of jejunal mucosae to posthatch chronic heat stress in broiler chickens. Poult Sci 2020;99:2727-35. https://doi.org/10.1016/j.psj.2019.12.038
  15. Ncho CM, Goel A, Jeong CM, Gupta V, Choi YH. Effects of in ovo feeding of γ-aminobutyric acid on growth performances, plasma metabolites, and antioxidant status in broilers exposed to cyclic heat stress. Sustainability 2021;13:11032. https://doi.org/10.3390/su131911032
  16. Goel A, Ncho CM, Jeong CM, Choi YH. Embryonic thermal manipulation and in ovo gamma-aminobutyric acid supplementation regulating the chick weight and stress-related genes at hatch. Front Vet Sci 2022;8:807450. https://doi.org/10.3389/fvets.2021.807450
  17. Zhang H, Elliott KEC, Durojaye OA, Fatemi SA, WSchilling M, Peebles ED. Effects of in ovo injection of L-ascorbic acid on growth performance, carcass composition, plasma antioxidant capacity, and meat quality in broiler chickens. Poult Sci 2019;98:3617-25. https://doi.org/10.3382/ps/pez173
  18. Slawinska A, Dunislawska A, Plowiec A, Goncalves J, Siwek M. TLR-mediated cytokine gene expression in chicken peripheral blood mononuclear cells as a measure to characterize immunobiotics. Genes 2021;12:195. https://doi.org/10.3390/genes12020195
  19. Soleimani AF, Zulkifli I, Omar AR, Raha AR. Physiological responses of 3 chicken breeds to acute heat stress. Poult Sci 2011;90:1435-40. https://doi.org/10.3382/ps.2011-01381
  20. Surai PF, Kochish, II, Fisinin VI, Kidd MT. Antioxidant defence systems and oxidative stress in poultry biology: an update. Antioxidants 2019;8:235. https://doi.org/10.3390/antiox8070235
  21. Kirkman HN, Gaetani GF. Catalase: a tetrameric enzyme with four tightly bound molecules of NADPH. Proc Natl Acad Sci 1984;81:4343-7. https://doi.org/10.1073/pnas.81.14.4343
  22. Surai P, Kochish I, Fisinin V. Antioxidant systems in poultry biology: nutritional modulation of vitagenes. Eur Poult Sci 2017;81:214. https://doi.org/10.1399/eps.2017.214
  23. Al Wakeel RA, Shukry M, Abdel Azeez A, Mahmoud S, Saad MF. Alleviation by gamma amino butyric acid supplementation of chronic heat stress-induced degenerative changes in jejunum in commercial broiler chickens. Stress 2017;20:562-72. https://doi.org/10.1080/10253890.2017.1377177
  24. Chen Z, Tang J, Sun YQ, Xie J. Protective effect of γ-aminobutyric acid on antioxidation function in intestinal mucosa of Wenchang chicken induced by heat stress. J Anim Plant Sci 2013;23:1634-41.
  25. Walls AB, Waagepetersen HS, Bak LK, Schousboe A, Sonnewald U. The glutamine-glutamate/GABA cycle: function, regional differences in glutamate and GABA production and effects of interference with GABA metabolism. Neurochem Res 2015;40:402-9. https://doi.org/10.1007/s11064-014-1473-1
  26. Al-Zghoul MB, Sukker H, Ababneh MM. Effect of thermal manipulation of broilers embryos on the response to heatinduced oxidative stress. Poult Sci 2019;98:991-1001. https:// doi.org/10.3382/ps/pey379
  27. Saleh KM, Tarkhan AH, Al-Zghoul MB. Embryonic thermal manipulation affects the antioxidant response to post-hatch thermal exposure in broiler chickens. Animals 2020;10:126. https://doi.org/10.3390/ani10010126
  28. Zaefarian F, Abdollahi MR, Cowieson A, Ravindran V. Avian liver: the forgotten organ. Animals 2019;9:63. https://doi.org/10.3390/ani9020063
  29. Hicks JA, Trakooljul N, Liu HC. Discovery of chicken microRNAs associated with lipogenesis and cell proliferation. Physiol Genomics 2010;41:185-93. https://doi.org/10.1152/ physiolgenomics.00156.2009
  30. Wang G, Kim WK, Cline MA, Gilbert ER. Factors affecting adipose tissue development in chickens: a review. Poult Sci 2017;96:3687-99. https://doi.org/10.3382/ps/pex184
  31. Ohta Y, Kidd MT. Optimum site for in ovo amino acid injection in broiler breeder eggs. Poult Sci 2001;80:1425-9. https://doi.org/10.1093/ps/80.10.1425
  32. Narinc D, Erdogan S, Tahtabicen E, Aksoy T. Effects of thermal manipulations during embryogenesis of broiler chickens on developmental stability, hatchability and chick quality. Animal 2016;10:1328-35. https://doi.org/10.1017/S1751731116000276
  33. Piestun Y, Halevy O, Yahav S. Thermal manipulations of broiler embryos-The effect on thermoregulation and development during embryogenesis. Poult Sci 2009;88:2677-88. https://doi.org/10.3382/ps.2009-00231
  34. Kadam MM, Bhanja SK, Mandal AB, et al. Effect of in ovo threonine supplementation on early growth, immunological responses and digestive enzyme activities in broiler chickens. Br Poult Sci 2008;49:736-41. https://doi.org/10.1080/00071660802469333
  35. Piestun Y, Halevy O, Shinder D, Ruzal M, Druyan S, Yahav S. Thermal manipulations during broiler embryogenesis improves post-hatch performance under hot conditions. J Therm Biol 2011;36:469-74. https://doi.org/10.1016/j.jtherbio.2011.08.003
  36. Riras A, Fabricant J. Indication of immunodepression in chicken infected with various strain of Marck's dsease virus. Avian Dis 1988;32:1-8. https://doi.org/10.2307/1590941
  37. Tang J, Chen Z. The protective effect of gamma-aminobutyric acid on the development of immune function in chickens under heat stress. J Anim Physiol Anim Nutr (Berl) 2016;100:768-77. https://doi.org/10.1111/jpn.12385
  38. Jin Z, Mendu SK, Birnir B. GABA is an effective immuno-modulatory molecule. Amino Acids 2013;45:87-94. https:// doi.org/10.1007/s00726-011-1193-7