Investigating the effect of different sources and levels of zinc on the immune performance and antioxidant capacity of laying hens

Document Type : Original Article

Authors
Department of Animal Science, Faculty of Agriculture, Shahrekord University, Shahrekord, Iran
10.22034/ijvcs.2023.14546.1062
Abstract
This experiment was conducted for 10 weeks (40 to 52 weeks old) to investigate the effect of different sources and levels of zinc on the immune and antioxidant performance of laying hens. For this purpose, 240 high-line laying hens (36-W) were used in a completely randomized design, with 8 treatments and 5 replications (6 birds per replication). The experimental treatments include 1- control (without zinc supplement), treatment 2, 3, and 4, respectively, including the control diet + 80, 120, and 160 mg/kg of zinc sulfate with a purity of 34%, and treatment 5, 6 and 7, respectively The control diet included 50, 75 and 100 mg/kg zinc hydroxy chloride with 55% purity, and treatment 8 included the control diet + 124 mg/kg zinc-methionine complex. The findings showed that, in general, different levels of zinc supplementation in organic and hydroxy form caused significant improvement in feed conversion ratio, shell weight, Haugh unit, and blood glucose reduction compared to other treatments. During the test, organic and hydroxy sources increased antibodies against the influenza vaccine (P<0.05). Also, treatments containing zinc supplements increased superoxide dismutase and total antioxidant capacity (P<0.05). This increase was associated with a decrease in serum malondialdehyde (P<0.05). Different levels and sources of zinc had no significant effect on shape index, yolk color, and glutathione peroxidase level (P<0.05). The results show that adding hydroxy chloride at 100 mg/kg can improve the antioxidant and safety indicators of eggs.
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1.   Abd El‐Hack M, Alagawany M, Amer S, Arif M, Wahdan KM, El‐Kholy M. Effect of dietary supplementation of organic zinc on laying performance, egg quality and some biochemical parameters of laying hens. Journal of animal physiology and animal nutrition. 2018;102(2):e542-e9.
2.   Abedini M, Shariatmadari F, Torshizi MAK, Ahmadi H. Effects of Zinc Oxide Nanoparticles on Performance, Egg Quality, Tissue Zinc Content, Bone Parameters, and Antioxidative Status in Laying Hens. Biol Trace Elem Res. 2018;184(1):259-67.
3.   Bahakaim A, Abdel Magied H, Osman S, Omar A, Abdelmalak N, Ramadan N. Effect of using different levels and sources of zinc in layer's diets on egg zinc enrichment. Egyptian Poultry Science Journal. 2014;34(1):39-56.
4.   Chen W, Wang S, Zhang HX, Ruan D, Xia WG, Cui YY, et al. Optimization of dietary zinc for egg production and antioxidant capacity in Chinese egg-laying ducks fed a diet based on corn-wheat bran and soybean meal. Poult Sci. 2017;96(7):2336-43.
5.   Cornescu GM, Panaite TD, Untea AE, Varzaru I, Saracila M, Dumitru M, et al. Mitigation of heat stress effects on laying hens' performances, egg quality, and some blood parameters by adding dietary zinc-enriched yeasts, parsley, and their combination. Frontiers in Veterinary Science. 2023;10:1202058.
6.   Cunningham-Rundles S, Cunningham-Rundles W, Chandra R. Nutrition and Immunology. RK Chandra, Ed. 1988;197.
7.   Davis G. Copper, inTrace Elements in Human and Animal Nutrition, W. Mertz, ed. Academic Press, San Diego, CA; 1987.
8.   Finkel T, Holbrook NJ. Oxidants, oxidative stress and the biology of ageing. Nature. 2000;408(6809):239-47.
9.   Fraker PJ, Haas SM, Luecke RW. Effect of zinc deficiency on the immune response of the young adult A/J mouse. The Journal of nutrition. 1977;107(10):1889-95.
10. Hassan S, Sharif M, Mirza MA, Rehman MSu. Effect of Dietary Supplementation of Zinc Nanoparticles Prepared by Different Green Methods on Egg Production, Egg Quality, Bone Mineralization, and Antioxidant Capacity in Caged Layers. Biological Trace Element Research. 2023:1-11.
11. Hudson B, Dozier III W, Fairchild B, Wilson J, Sander J, Ward T. Live performance and immune responses of straight-run broilers: influences of zinc source in broiler breeder hen and progeny diets and ambient temperature during the broiler production period. Journal of applied poultry research. 2004;13(2):291-301.
12. International H-L. Hy‐Line W36 commercial management guide. Hy-Line International West Des Moines, IA; 2007.
13. Jensen C, Engberg R, Jakobsen K, Skibsted L, Bertelsen G. Influence of the oxidative quality of dietary oil on broiler meat storage stability. Meat Science. 1997;47(3-4):211-22.
14. Junchang C, Ruangpanit Y. Effects of organic zinc and manganese supplementation on eggshell quality and bone characteristic of laying hens during late laying cycle. Agriculture and Natural Resources. 2023;57(1):145–52-–52.
15. Karami M, Torki M, Mohammadi H. Effects of dietary supplemental chromium methionine, zinc oxide, and ascorbic acid on performance, egg quality traits, and blood parameters of laying hens subjected to heat stress. Journal of applied animal research. 2018;46(1):1174-84.
16. Keshavarz K. A comparison between cholecalciferol and 25-OH-cholecalciferol on performance and eggshell quality of hens fed different levels of calcium and phosphorus. Poultry science. 2003;82(9):1415-22.
17. Li L, Abouelezz KFM, Gou Z, Lin X, Wang Y, Fan Q, et al. Optimization of Dietary Zinc Requirement for Broiler Breeder Hens of Chinese Yellow-Feathered Chicken. Animals (Basel). 2019;9(7).
18. Li LL, Gong YJ, Zhan HQ, Zheng YX, Zou XT. Effects of dietary Zn-methionine supplementation on the laying performance, egg quality, antioxidant capacity, and serum parameters of laying hens. Poultry Science. 2019;98(2):923-31.
19. Liu X, Lin X, Mi Y, Li J, Zhang C. Grape Seed Proanthocyanidin Extract Prevents Ovarian Aging by Inhibiting Oxidative Stress in the Hens. Oxid Med Cell Longev. 2018;2018:9390810.
20. Mabe I, Rapp C, Bain M, Nys Y. Supplementation of a corn-soybean meal diet with manganese, copper, and zinc from organic or inorganic sources improves eggshell quality in aged laying hens. Poultry science. 2003;82(12):1903-13.
21. Marquardt WW, Snyder DB, Savage PK, Kadavil SK, Yancey FS. Antibody response to Newcastle disease virus given by two different routes as measured by ELISA and hemagglutination-inhibition test and associated tracheal immunity. Avian Dis. 1985;29(1):71-9.
22. Martin KM. The effects of zinc supplementation from two sources on egg quality and bone health in laying hens. 2016.
23. mikaeili e, kafilzade f, chaharaeen B, Khamisabadi H, kiani a. Effect of Vitamin E alone or with Selenium injection during late pregnancy on Colostrum and Serum Se, Cu, Zn and Fe concentrations of ewes and their lambs. Iranian Journal of Veterinary Clinical Sciences. 2019;12(2):-.
24. Neto MT, Dadalt J, Tse M. Dietary combination of chelated zinc and threonine and effects on egg production, egg quality and nutrient balance of Brown laying hens from 20 to 49 weeks of age. Animal Feed Science and Technology. 2020;267:114555.
25. Nielsen F, Mikkelsen BB, Nielsen JB, Andersen HR, Grandjean P. Plasma malondialdehyde as biomarker for oxidative stress: reference interval and effects of life-style factors. Clinical chemistry. 1997;43(7):1209-14.
26. Nonkookhetkhong T, Chalalai T. Effect of zinc hydroxychloride supplementation combined with an anticoccidial drug on Eimeria tenella infection in broiler chickens. Veterinary World. 2023;16(4):675.
27. Noor R, Mittal S, Iqbal J. Superoxide dismutase--applications and relevance to human diseases. Med Sci Monit. 2002;8(9):Ra210-5.
28. Nys Y, Gautron J, McKee M, Garcia-Ruiz J, Hincke M. Biochemical and functional characterisation of eggshell matrix proteins in hens. World's Poultry Science Journal. 2001;57(4):401-13.
29. Ogbuewu I, Modisaojang-Mojanaga M, Mokolopi B, Mbajiorgu C. A meta-analysis of responses of broiler chickens to dietary zinc supplementation: feed intake, feed conversion ratio and average daily gain. Biological Trace Element Research. 2023;201(5):2491-502.
30. Orr WC, Sohal RS. Extension of life-span by overexpression of superoxide dismutase and catalase in Drosophila melanogaster. Science. 1994;263(5150):1128-30.
31. Ōyanagui Y. Reevaluation of assay methods and establishment of kit for superoxide dismutase activity. Analytical biochemistry. 1984;142(2):290-6.
32. Pal D, Gowda N, Prasad C, Amarnath R, Bharadwaj U, Babu GS, et al. Effect of copper-and zinc-methionine supplementation on bioavailability, mineral status and tissue concentrations of copper and zinc in ewes. Journal of Trace Elements in Medicine and Biology. 2010;24(2):89-94.
33. Placer ZA, Cushman LL, Johnson BC. Estimation of product of lipid peroxidation (malonyl dialdehyde) in biochemical systems. Analytical biochemistry. 1966;16(2):359-64.
34. Qi X, Ma S, Liu X, Wang Y, Liu Y, Gao Y, et al. Effects of the methionine hydroxyl analogue chelate zinc on antioxidant capacity and liver metabolism using 1H-NMR-based metabolomics in aged laying hens. Animals. 2019;9(11):898.
35. Rahman MM, Wahed MA, Fuchs GJ, Baqui AH, Alvarez JO. Synergistic effect of zinc and vitamin A on the biochemical indexes of vitamin A nutrition in children. The American journal of clinical nutrition. 2002;75(1):92-8.
36. Sajadifar S, Miranzadeh H, Moazeni M. Effect of zinc on humoral and cell-mediated immunity of broilers vaccinated against coccidiosis. Iranian Journal of Parasitology. 2013;8(3):474.
37. SAS Institute (2003) SAS/STAT® User’s Guide: Statistics Version 6.12. SAS Institute Inc., Cary, NC.
38. Stefanidou M, Maravelias C, Dona A, Spiliopoulou C. Zinc: a multipurpose trace element. Archives of toxicology. 2006;80:1-9.
39. Stevenson MJ, Janisse SE, Tao L, Neil RL, Pham QD, Britt RD, et al. Elucidation of a Copper Binding Site in Proinsulin C-peptide and Its Implications for Metal-Modulated Activity. Inorganic Chemistry. 2020;59(13):9339-49.
40. Surai PF. Antioxidant systems in poultry biology: superoxide dismutase. Journal of Animal Research and Nutrition. 2016;1(1):8.
41. Tobia MH, Zdanowicz MM, Wingertzahn MA, McHeffey-Atkinson B, Slonim AE, Wapnir RA. The role of dietary zinc in modifying the onset and severity of spontaneous diabetes in the BB Wistar rat. Molecular Genetics and Metabolism. 1998;63(3):205-13.
42. Underwood E, Suttle N. The mineral nutrition of livestock 3rd edition. CABI; 1999.
43. Vieira SL. Chelated minerals for poultry. Brazilian Journal of Poultry Science. 2008;10:73-9.
44. Younas Z, Mashwani ZUR, Ahmad I, Khan M, Zaman S, Sawati L, et al. Mechanistic Approaches to the Application of Nano-Zinc in the Poultry and Biomedical Industries: A Comprehensive Review of Future Perspectives and Challenges. Molecules. 2023;28(3):1064.
45. Zhang K, Han M, Dong Y, Miao Z, Zhang J, Song X, et al. Low levels of organic compound trace elements improve the eggshell quality, antioxidant capacity, immune function, and mineral deposition of aged laying hens. Animal. 2021;15(12):100401.
46. Zhao CY, Tan SX, Xiao XY, Qiu XS, Pan JQ, Tang ZX. Effects of dietary zinc oxide nanoparticles on growth performance and antioxidative status in broilers. Biol Trace Elem Res. 2014;160(3):361-7.