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Nano zinc supplementation in ruminant’s livestock, influence on physiological, immune functions and oxidative stability of West African dwarf goat bucks

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Abstract

The recent temperature extremes and other associated climatic events pose a detrimental effect to ruminant livestock. To abate this, it is necessary to adopt a functional (biotechnology) approach like the use of nano minerals as feed additives for normal immune function. Nano zinc oxide (nZnO) has demonstrated growth-promoting properties and has been reported to improve antioxidant capacities with high bioavailability recorded in ruminant. This study therefore aimed to research into nano zinc supplementation on growth performance, haematology, serum, oxidative and antioxidant enzymes of West African dwarf (WAD) goats. A total of 18 yearling WAD goats (7.2 ± 0.54 kg) were allocated into 3 treatments of 6 animals per treatment on weight equalization bases. Each group was randomly allotted to three (0, 300 and 600 mg/kg nZnO) experimental diets. Data on haematological parameters, serum minerals and serum biochemical parameters were collected on day 0 and day 84 of the experiment. Data collected were subjected to analysis of variance in a completely randomized design (CRD), and significant means were separated using Tukey’s test. It was revealed that West African dwarf goats fed 600 mg/kg nZnO recorded the highest (p < 0.05) PCV and white blood cell values (32.00% and 5.70 × 103/L, respectively) while goats fed 300 mg/kg nZnO recorded the lowest values. At day 84, nZnO supplementation increased serum total protein, globulin and total cholesterol concentration, with higher values (7.57 g/dl, 4.17 g/dl and 95.73 mg/dl) recorded for goats fed 300 mg/kg nZnO. Lower aspartate aminotransferase (66.33 U/L) was observed for goats fed diets containing 300 g/kg nano zinc oxide. Serum minerals (phosphorus, zinc, copper and iron) were elevated in 600 mg/kg nZnO group. Supplementation of nZnO had no significant (p > 0.05) effect on blood superoxide dismutase (SOD) and total bilirubin concentration while reduced (p < 0.05) malondialdehyde (MDA) and urea values were recorded in 300 and 600 mg/kg nZnO supplemented treatments. Goats fed 600 mg/kg nZnO recorded a lower (p < 0.05) glutathione peroxidase value for kidney (24.78 U/mg) and forelimb cut (24.89 U/mg) while kidney, liver and forelimb cut SOD values (4.61, 2.45 and 5.84 U/mg, respectively) were highest at 300 mg/kg nZnO group. The study concluded that supplemented nZnO aided maintenance of and improved the health of the experimental animals through elevated PCV, serum parameters, reduced MDA, urea and other oxidative biomarkers in both serum and organs of West African dwarf goats.

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References

  • Aditia M, Sunarso L, Sevilla CC, Angeles AA (2014) Growth performance and mineral status on goats (Capra hircus linn) supplemented with zinc proteinate and selenium yeast. Int J Sci Eng 7:124–129

  • Akbari MR, Kermanshahi H, Moghaddam HN, Moussavi AH, Afshari JT (2008) Effects of wheat-soybean meal-based diet supplementation with vitamin A, vitamin E and zinc on blood cells, organ weights and humoral immune response in broiler chickens. J Anim Vet Adv 7(3):297–304

    Google Scholar 

  • Akhigbe R, Ajayi A (2020) Testicular toxicity following chronic codeine administration is via oxidative DNA damage and up-regulation of NO/TNF-α and caspase 3 activities. PloS one 1I5(3):pe0224052

  • Akuru EA (2017) Performance, bone mineralization and haematological indices of broilers fed phytogenic feed additives (Doctoral dissertation)

  • Abule RTS, Etebu E (2017) Biodiversity of bacteria identified from 16s bacterial DNA sequences amplified from broiler gut digesta. In Proceedings of 6th ASAN-NIAS Joint Annual Meeting Septembe (10):14

  • Alimohamady R, Aliarabi H, Bruckmaier RM, Christensen RG (2019) Effect of different sources of supplemental zinc on performance, nutrient digestibility, and antioxidant enzyme activities in lambs. Biol Trace Elem Res 189(1):75–84

    CAS  PubMed  Google Scholar 

  • Allain CC, Poon LS, Chan CS, Richmond WFPC, Fu PC (1974) Enzymatic determination of total serum cholesterol. Clin Chem 20(4):470–475

    CAS  PubMed  Google Scholar 

  • Ammerman CB, Baker DH, Lewis AJ (1995) Bioavailability of nutrients for animals: amino acids, minerals, and vitamins. Academic Press, New York

    Google Scholar 

  • Andrieu S (2008) Is there a role for organic trace element supplements in transition cow health? Vet J 176:77–83

    CAS  PubMed  Google Scholar 

  • Bao YM, Choct M (2009) Trace Mineral Nutrition for Broiler Chickens and Prospects of Application of Organically Complexed Trace Minerals: a Review Anim Prod Sci 49:269–282

    CAS  Google Scholar 

  • Barham D, Trinder P (1972) An improved colour reagent for the determination of blood glucose by the oxidase system. Analyst 97(1151):142–145

    CAS  PubMed  Google Scholar 

  • Bartels H, Bohmer M (1972) Clin Chem Acta 37:193

    CAS  Google Scholar 

  • Benjamin DR, Shunk B (1978) A fatal case of peliosis of the liver and spleen. Am J Dis Child 132(2):207–208

    CAS  PubMed  Google Scholar 

  • Beppu F, Niwano Y, Tsukui T, Hosokawa M, Miyashita K (2009) Single and repeated oral dose toxicity study of fucoxanthin (FX), a marine carotenoid, in mice. J Toxicol Sci 34(5):501–510

    CAS  PubMed  Google Scholar 

  • Berg JM, Shi Y (1996) The galvanization of biology: a growing appreciation for the roles of zinc. Science 271(5252):1081–1085

    CAS  PubMed  Google Scholar 

  • Beutler E, Duron O, Kelly BM (1975) Improved method for the determination of blood glutathione. J Lab Clin Med 61:882–888

    Google Scholar 

  • Buege JA, Aust SD (1978) Microsomal Lipid Peroxidation Methods Enzymol 52:302

    CAS  PubMed  Google Scholar 

  • Burman U, Saini M, Kumar P (2013) Effect of zinc oxide nanoparticles on growth and antioxidant system of chickpea seedlings. Toxicol Environ Chem 95(4):605–612

    CAS  Google Scholar 

  • Chen K, Xu W, Wilson M, He B, Miller NW, Bengten E, Edholm ES, Santini PA, Rath P, Chiu A, Cattalini M (2009) Immunoglobulin D enhances immune surveillance by activating antimicrobial, proinflammatory and B cell–stimulating programs in basophils. Nat Immunol 10(8):889–898

    CAS  PubMed  PubMed Central  Google Scholar 

  • Coles EH (1986) Veterinary clinical pathology. 4th Edition WB Saunders Co Philadelphia, p 498–517

  • Cunningham-Rundles S, Bockman RS, Lin A, Giardina PV, Hilgartner MW, Caldwell BD, Carter DM (1990) Physiological and pharmacological effects of zinc on immune response. Ann New York Acad Sci 587, 113–122

  • Daghsh HA, Mousa SM (1999) Zinc sulfate supplementation to ruminant rations and its effects on digestibility in lambs; growth, rectal temperature and some blood constituents in buffalo calves under heat stress. Assiut Vet Med J 40:128–146

    Google Scholar 

  • Daramola JO, Adeloye AA, Fatoba TA, Soladoye AO (2005) Haematological and Biochemical Parameters of West African Dwarf Goats Livest Res Rural Dev 17(8):95

    Google Scholar 

  • Dawei AI, Zhisheng W, Anguo Z (2010) Protective effects of nano-ZnO on the primary culture mice intestinal epithelial cells in in vitro against oxidative injury. World J Agric Res 6(2):149–153

    Google Scholar 

  • Elamin KM, Dafalla NA, Atti KA, Eldar AA (2013) Effects of zinc supplementation on growth performance and some blood parameters of goat kids in Sudan. Int J Pure Appl Biosci 1(1):1–8

    Google Scholar 

  • Evans EW, Duncan JR (2011) Proteins, lipids, and carbohydrates. Duncan and Prasse’s Veterinary Laboratory Medicine Clinical Pathology, Ed 5:173–210

    Google Scholar 

  • Fadayifar A, Aliarabi H, Tabatabaei MM, Zamani P, Bahari A, Malecki M, Dezfoulian AH (2012) Improvement in lamb performance on barley-based diet supplemented with zinc. Livest Sci 144(3):285–289

    Google Scholar 

  • Farrugia A, Penrod J, Bult JM (2010) Payment, compensation and replacement–the ethics and motivation of blood and plasma donation. Vox Sanguinis 99(3):202–211

  • Feldman HA, Longcope C, Derby CA, Johannes CB, Araujo AB, Coviello AD, Bremner WJ, McKinlay JB (2002) Age trends in the level of serum testosterone and other hormones in middle-aged men: longitudinal results from the Massachusetts male aging study. J Clin Endocrinol Metab 87(2):589–598

    CAS  PubMed  Google Scholar 

  • Gaafar HMA, Bassiouni MI, Ali MFE, Shitta AA, Shamas ASE (2011) Effect of zinc methionine supplementation on productive performance of lactating Friesian cows. J Anim Sci Biotech 2(2):94–101

    Google Scholar 

  • García-Giménez JL, Roma-Mateo C, Perez-Machado G, Peiro-Chova L, Pallardó FV (2017) Role of glutathione in the regulation of epigenetic mechanisms in disease. Free Radic Biol Med 112:36–48

    PubMed  Google Scholar 

  • Garg AK, Mudgal V, Dass RS (2008) Effect of organic zinc supplementation on growth, nutrient utilization and mineral profile in lambs. Ani Feed Sci Technol 144(1–2):82–96

    CAS  Google Scholar 

  • Ghosh A, Mandal GP, Roy A, Patra AK (2016) Effects of supplementation of manganese with or without phytase on growth performance, carcass traits, muscle and tibia composition, and immunity in broiler chickens. Livest Sci 191:80–85

    Google Scholar 

  • Gornall AG, Bardawill CJ, David MM (1949) Determination of serum proteins by means of the biuret reaction. J Biol Chem 1;177(2):751–66

  • Greene LW, Lunt DK, Byers FM, Chirase NK, Richmond CE, Knutson RE, Schelling GT (1988) Performance and carcass quality of steers supplemented with zinc oxide or zinc methionine. J Ani Sci 66(7):1818–1823

  • Guan T, Song J, Wang Y, Guo L, Yuan L, Zhao Y, Gao Y, Lin L, Wang Y, Wei J (2017) Expression and characterization of recombinant bifunctional enzymes with glutathione peroxidase and superoxide dismutase activities. Free Radic Biol Med 110:188–195

    CAS  PubMed  Google Scholar 

  • Habig WH, Pabst MJ, Jakoby WB (1974) Glutathione S-transferases: the first enzymatic step in mercapturic acid formation. J Bio Chem 249(22):7130–7139

    CAS  Google Scholar 

  • Haenlein GFW, Anke M (2011) Mineral and trace element research in goats: a review. Small Rumin Res 95:2–19

    Google Scholar 

  • Harpur E, Ennulat D, Hoffman D, Betton G, Gautier JC, Riefke B, Bounous D, Schuster K, Beushausen S, Guffroy M, Shaw M (2011) Biological qualification of biomarkers of chemical-induced renal toxicity in two strains of male rat. Toxicol SCi 2(2):235–252

    Google Scholar 

  • Hassan AA, Ashry GME, Soliman SM (2011) Effect of supplementation of chelated zinc on milk production in ewes. Food Nut Sci 2:706–713

    CAS  Google Scholar 

  • Hatfield PG, Swenson CK, Kott RW, Ansotegu, RP, Roth NJ, Robinson BL (2001) Zinc and copper status in ewes supplemented with sulfate-and amino acid-complexed forms of zinc and copper. J Sci 79(1):261–266

  • Heidari J, Seifdavati J, Mohebodini H, Sharifi RS, Benemar HA (2018) Effect of nano zinc oxide on post-thaw variables and oxidative status of Moghani ram semen. Kafkas Univ Vet Fak Derg 25(1)

  • Huerta M, Kincaid RL, Cronrath JD, Busboom J, Johnson AB, Swenson CK (2002) Interaction of dietary zinc and growth implants on weight gain, carcass traits and zinc in tissues of growing beef steers and heifers. Anim Feed Sci Technol 95(1):15–32

    CAS  Google Scholar 

  • Jain J, McCafffrey PG, Miner Z, Kerppola TK, Lambert JN, Verdine GL, Curran T, Rao A (1993) The T-cell transcription factor NFAT p is a substrate for calcineurin and interacts with Fos and Jun. Nature 365(6444):352–355

    CAS  PubMed  Google Scholar 

  • Janknegt PJ, Rijstenbil JW, Van de Poll WH, Gechev TS, Buma AG (2007) A comparison of quantitative and qualitative superoxide dismutase assays for application to low temperature microalgae. J Photochem Photobiol b: Biol 87(3):218–226

    CAS  Google Scholar 

  • Jarosz M, Olbert M, Wyszogrodzka G, Młyniec K, Librowski T (2017) Antioxidant and anti-inflammatory effects of zinc zinc-dependent NF-κB signaling. Inflammopharmacology 25(1):11–24

    CAS  PubMed  PubMed Central  Google Scholar 

  • Jia W, Zhu X, Zhang W, Cheng J, Guo C, Jia Z (2009) Effects of source of supplemental zinc on performance, nutrient digestibility and plasma mineral profile in Cashmere goats. Asian-Australias J Anim Sci 22(12):1648–1653

    CAS  Google Scholar 

  • Jollow DJ, Mitchell JR, Zampaglione N, Gillette JR (1974) Bromobenzene-induced liver necrosis protective role of glutathione and evidence for 3, 4-bromobenzene oxide as the hepatotoxic metabolite. Pharmacol 11(3):151–169

    CAS  Google Scholar 

  • Joshua PP, Valli C, Balakrishnan V (2016) Effect of in vivo supplementation of nano forms of zinc, copper, and selenium on posthatch performance of broiler chicken. Vet World 9:287–294

    CAS  PubMed  PubMed Central  Google Scholar 

  • Kegley EB, Silzell SA, Kreider DL, Galloway DL, Coffey KP, Hornsby JA, Hubbell DS (2001) The immune response and performance of calves supplemented with zinc from an organic and an inorganic. Source11Published with the approval of the director of the Arkansas Agricultural Experiment Station, manuscript no 00075. The Prof Ani Sci 17(1):33–38

  • Kwari ID, Igwebuike JU, Mohammed ID, Diarra SS (2011) Growth, haematology and serum chemistry of broiler chickens fed raw or differently processed sorrel (Hibiscus Sabdariffa) seed meal in a semiarid environment. Int J Sci Nat 2(1):22–27

    CAS  Google Scholar 

  • Llobet JM, Domingo JL, Colomina MT et al (1988) Subchronic oral toxicity of zinc in rats. Bull Environ Contam Toxicol 41(1): 36–43

  • Mandal GP, Dass RS (2010) Haemato-Biochemical Profile of Crossbred Calves Supplemented with Inorganic and Organic Source of Zinc Indian J Anim Res 44(3):197–200

    Google Scholar 

  • Mandal GP, Dass RS, Isore DP, Garg AK, Ram GC (2007) Effect of zinc supplementation from two sources on growth, nutrient utilization and immune response in male crossbred cattle (Bos indicus × Bos taurus) bulls. Anim Feed Tech 138:1–12

    CAS  Google Scholar 

  • Merck M (2011) Hematological and serum biochemical reference guides. Merck Veterinary Manual 10th ed online version, Merck Sharp & Dohme Carp, a subsidiary of Merck & Co, Inc Whitehouse Station, NJ, USA

  • Misra HP, Fridovic I (1972) The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase. J Biol Chem 247:3170–3175

    CAS  PubMed  Google Scholar 

  • Mohamed MY, Ibrahim K, Abd El Ghany FT, Mahgoup AAS (2017) Impact of nano-zinc oxide supplementation on productive performance and some biochemical parameters of ewes and offspring Egypt J Sheep and Goats. Sci 12(3):1–16

    Google Scholar 

  • Nagalakshmi D, Dhanalakshmi K, Himabindu D (2009) Effect of dose and source of supplemental zinc on immune response and oxidative enzymes in lambs. Vet Res Com 33(7):631–644

    CAS  Google Scholar 

  • Najafzadeh H, Ghoreishi SM, Mohammadian B, Rahimi E, Afzalzadeh MR, Kazemivarnamkhasti, M, Ganjealidarani H (2013) Serum biochemical and histopathological changes in liver and kidney in lambs after zinc oxide nanoparticles administration. Vet World 6(8)

  • Nedredal GI, Amiot BP, Nyberg P, Luebke-Wheeler J, Lillegard JB, McKenzie TJ, Nyberg SL (2009) Optimization of mass transfer for toxin removal and immunoprotection of hepatocytes in a bioartificial liver. Biotechnol Bioeng 104(5):995

    CAS  PubMed  PubMed Central  Google Scholar 

  • O’Dell BL (1997) Mineral-ion interaction as assessed by bioavailability and ion channel function. In: O’Dell BL, Sunde RA (eds) Handbook of nutritionally essential mineral elements. Marcel Dekker, New York, pp 641–659

    Google Scholar 

  • Oyagbemi AA, Omobowale TO, Akinrinde AS, Saba AB, Ogunpolu BS, Daramola O (2015) Lack of reversal of oxidative damage in renal tissues of lead acetate-treated rats. Environ Toxicol 30(11):1235–1243

    PubMed  Google Scholar 

  • Parashuramulu S, Nagalakshmi D, Srinivasa Rao D, Kishan Kumar M, Swain PS (2015) Effect of zinc supplementation on antioxidant status and immune response in buffalo calves. Anim Nutr Feed Technol 15(2):179e88 Effect of nano zinc oxide on zinc bioavailability and blood biochemical changes in pre-ruminant lambs

  • Phiri ECJH, Viva M, Chibunda RT, Mellau LSB (2009) Effect of zinc supplementation on plasma mineral concentration in grazing goats in sub-humid climate of Tanzania. Tanzania Vet J 26(2):92–96

  • Rao AK, Shaha C (2000) Role of glutathione S-transferases in oxidative stress–induced male germ cell apoptosis. Free Radic Biol Med 29(10):1015–1027

    CAS  PubMed  Google Scholar 

  • Rimbach G, Walter A, Most E, Pallauf J (1998) Effect of microbial phytase on zinc bioavailability and cadmium and lead accumulation in growing rats. Food Chem Toxicol 36:7–12

    CAS  PubMed  Google Scholar 

  • Sidhu P, Garg ML, Dhawan DK (2005) Protective effects of zinc on oxidative stress enzymes in liver of protein-deficient rats. Drug Chem Toxicol 28(2):211–230

  • Singh KK, Maity SB, Maity A (2018) Indian J of Ani Sci 88(7):805–807

    CAS  Google Scholar 

  • Sobhanirad S, Naserian AA (2012) Effects of high dietary zinc concentration and zinc sources on hematology and biochemistry of blood serum in Holstein dairy cows. Anim Feed Sci Tech 177(3):242–246

    CAS  Google Scholar 

  • Someya Y, Tanihata J, Sato S, Kawano F, Shirato K, Sugiyama M, Kawashima Y, Nomura S, Tachiyashiki K, Imaizumi K (2009) Zinc-deficiency induced changes in the distribution of rat white blood cells. J Nutr Sci Vitaminol 55(2):162–169

    CAS  PubMed  Google Scholar 

  • Suttle NF (2010) The mineral nutrition of livestock, 4th edn. CABI Publishing, Oxfordshire

    Google Scholar 

  • Swain PS, Rao SB, Rajendran D, Dominic G, Selvaraju S (2016) Nano zinc, an alternative to conventional zinc as animal feed supplement: a review. Anim Nutr 2(3):134–141

  • Swain P, Das R, Das A, Padhi SK, Das KC, Mishra SS (2019) Effects of dietary zinc oxide and selenium nanoparticles on growth performance, immune responses and enzyme activity in rohu, Labeo rohita (Hamilton). Aquac Nutr 25(2):486–494

    CAS  Google Scholar 

  • Tavares-Dias M, Oliveira-Ju´ nior A, Marcon JL (2008) Methodological limitations of counting total leukocytes and thrombocytes in reptiles (Amazon turtle, Podocnemisexpansa): Ananalysis and discussion. Acta Amazonica 38:159–163

  • Thornton PK (2010) Livestock production: recent trends, future prospects. Philos Trans R Soc Lond B Biol Sci 365(1554):2853–2867

    PubMed  PubMed Central  Google Scholar 

  • Tsutsumi R, Ohashi K, Tsutsumi YM, Horikawa YT, Minakuchi J, Minami S, Harada N, Sakaue H, Sakai T, Nakaya Y (2014) Albumin-normalized serum zinc: a clinically useful parameter for detecting taste impairment in patients undergoing dialysis. Nut Res 34(1):11–16

    CAS  Google Scholar 

  • Varley H, Van E, Kass I (1980) Practical clinical chemistry, New York, Inter Science Varley Publishers Inc 197–240

  • Varshney R, Kale RK (1990) Effects of calmodulin antagonists on radiation-induced lipid peroxidation in microsomes. Int J Radiat Biol 58(5):733–743

    CAS  PubMed  Google Scholar 

  • Viveros A, Brenes A, Arija I, Centeno C (2002) Effects of microbial phytase supplementation on mineral utilization and serum enzyme activities in broiler chicks fed different levels of phosphorus. Poul Sci 81(8):1172–1183

  • Volpe CMO, Villar-Delfino PH, Dos Anjos PM, Nogueira-Machado JA (2018) Cellular death, reactive oxygen species (ROS) and diabetic complications Cell Death. Dis 9(2):1–9

    CAS  Google Scholar 

  • Walsh CT, Sandstead HH, Prasad ADS, Newberne PM, Fraker, PJ (1994) Zinc: health effects and research priorities for the 1990s. Environ Health Perspect 102(2):5–46

  • Wang ZL (2001) Characterization of nanophase materials. Particle & Particle Systems Characterization: Measurement and Description of Particle Properties and Behavior in Powders and Other Disperse Systems 18(3):142–165

  • Waziri MA, Ribadu AY, Sivachelvan N (2010) Change in the serum proteins, hematological and some serum biochemical profiles in the gestation period in the Sahel goats. Vet Arch 80:215–224

  • Wedekind KJ, Baker DH (1990) Zinc bioavailability in feed-grade. Sources of Zinc J Anim Sci 68:684–689

    CAS  PubMed  Google Scholar 

  • Weiss WP (2017) A 100-year review: from ascorbic acid to zinc—mineral and vitamin nutrition of dairy cows. J Dairy Sci 100:10045–10060

  • Wiering FT, Berger J, Dijkhuizen MA, Hidayat A, Ninh NX, Utomo B, Wasantwisut E, Winichaggon P (2007) Combined iron and zinc supplementation in infants improved iron and zinc status, but interactions reduced efficacy in a multicountry trial in Southeast. Asia J Nut 137:466–471

    Google Scholar 

  • Wright CL, Spears JW (2004) Effect of zinc source and dietary level on zinc metabolism in Holstein calves. J Dairy Sci 87:1085–1091

    CAS  Google Scholar 

  • Yadav AK, Kumar J, Anand M (2015) Effect of Dietary Zinc and Selenium Supplementation on Antioxidative Enzyme Profile of Barbari Goats Indian J Small Ruminants 21(1):46–48

    Google Scholar 

  • Yousef MI, El Hendy HA, El-Demerdash FM, Elagamy EI (2002) Dietary zinc deficiency induced-changes in the activity of enzymes and the levels of free radicals, lipids and protein electrophoretic behavior in growing rats. Toxicol 175(1–3):223–234

    CAS  Google Scholar 

  • Yusuf AO, Adeyi TK, Sowande OS, Oni AO, Olowookere VO (2022) Nano zinc oxide supplementation improves growth performance and health of West African dwarf goats. Egyptian Journal of Animal Production 59(2):69–78

    Google Scholar 

  • Yusuf AO, Mlambo V, Sowande OS, Solomon R (2017) Oxidative stress biomarkers in West African dwarf goats reared under intensive and semi-intensive production systems. S Afr J Anim Sci 47(3):281–289

    CAS  Google Scholar 

  • Zaboli K, Aliarabi H, Bahari AA, ABBAS AKR (2013) Role of dietary nano-zinc oxide on growth performance and blood levels of mineral: a study on in Iranian Angora (Markhoz) goat kids. J Pharma Res Health Sci 2(1):19–26

    Google Scholar 

  • Zhao CY, Tan SX, Xiao XY, Qiu XS, Pan JQ, Tang ZX (2014) Effects of dietary zinc oxide nanoparticles on growth performance and antioxidative status in broilers. Biol Trace Elem Res 160(3):361–367

    CAS  PubMed  Google Scholar 

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AOY, AOO and SOS conceived and decided on the experimental design; TKA performed the experiments; AJO analysed and interpreted the data; AOY and TKA wrote the paper, conceived and designed the experiments; AOY wrote the first draft of the manuscript which was proofread by AOO and SOS.

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Correspondence to Azeez Olanrewaju Yusuf.

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Yusuf, A.O., Adeyi, T.K., Oni, A.O. et al. Nano zinc supplementation in ruminant’s livestock, influence on physiological, immune functions and oxidative stability of West African dwarf goat bucks. Comp Clin Pathol 32, 629–643 (2023). https://doi.org/10.1007/s00580-023-03471-4

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