Efficacy of dietary supplementation of nanoparticles-chromium, chromium-methionine and zinc-proteinate, on performance of Japanese quail under physiological stress

References

• Adedapo AA, Saba AB, Dina OA, Oladejo GMA. 2004. Effects of dexamethasone on the infectivity of Trypanosoma vivax and serum biochemistry change in Nigerian domestic chickens. Veterinarski arhiv Trop J Anim Sci. 74(5):371–382.
   Google Scholar
• Aengwanich W. 2007. Effects of dexamethasone on physiological changes and productive performance in broilers. Asian J Anim Vet Adv. 32(2):157–161.
   Google Scholar
• Aengwanich W, Chinrasri O. 2003. Effect of dexamethasone on differential white blood cell counts and heterophil/lymphocyte ratio in Japanese quails (Coturnix coturnix japonica). Songklanakarin J Sci and Tech. 25:183–189.
   Google Scholar
• Ali M, Kang GH, Joo ST. 2008. A review: Influences of pre-slaughter stress on poultry meat quality. Asian Australas J Anim Sci. 21(6):912–916.
   Web of Science ®Google Scholar
• Attia YA, Abd Al-Hamid AE, Zeweil HS, Qota EM, Bovera F, Monastra G, Sahledom MD. 2013. Effect of dietary amounts of inorganic and organic zinc on productive and physiological traits of White Pekin ducks. Animal. 7(6):895–900.
   PubMed Web of Science ®Google Scholar
• Attia YA, Abd El AE, Abedalla AA, Berika MA, Al-Harthi MA, Kucuk O, Sahin K, Abou-Shehema BM. 2016. Laying performance, digestibility and plasma hormones in laying hens exposed to chronic heat stress as affected by betaine, vitamin C, and/or vitamin E supplementation. Springerplus. 5(1):1619.
   PubMedGoogle Scholar
• Attia YA, Abd-El-Hamid AE, ElKomy A, Shawky OM. 2013. Responses of productive, physiological and immunological traits of growing Fayoumi males subjected to heat stress to vitamin C and/or E and organic Zinc supplementation. J Agric Env Sci Dam Univ. 12(1):48–75.
   Google Scholar
• Attia YA, Addeo NF, Al-Hamid A, Bovera F. 2019. Effects of phytase supplementation to diets with or without zinc addition on growth performance and zinc utilization of white pekin ducks. Animals. 9(5):280.
   Web of Science ®Google Scholar
• Attia YA, Al-Harthi MA, Sh. Elnaggar A. 2018. Productive, physiological and immunological responses of two broiler strains fed different dietary regimens and exposed to heat stress. Ital J Anim Sci. 17(3):686–697.
   Web of Science ®Google Scholar
• Botsoglou NA, Florou-Paneri P, Christaki E, Fletouris DJ, Spais AB. 2002. Effect of dietary oregano essential oil on performance of chickens and on iron-induced lipid oxidation of breast, thigh and abdominal fat tissues. Br Poult Sci. 43(2):223–230.
   PubMed Web of Science ®Google Scholar
• Cai Y, Song Z, Zhang X, Wang X, Jiao H, Lin H. 2009. Increased de novo lipogenesis in liver contributes to the augmented fat deposition in dexamethasone exposed broiler chickens (Gallus gallus domesticus). Comp Biochem Physiol C Toxicol Pharmacol. 150(2):164–169.
   PubMed Web of Science ®Google Scholar
• Castellini C, Mugnai CA, Dal Bosco A. 2002. Effect of organic production system on broiler carcass and meat quality. Meat Sci. 60(3):219–225.
   PubMed Web of Science ®Google Scholar
• Davis AK, Maney DL, Maerz JC. 2008. The use of leukocyte profiles to measure stress in vertebrates: a review for ecologists. Funct Ecol. 22(5):760–772.
   Web of Science ®Google Scholar
• Gangadoo S, Dinev I, Chapman J, Hughes RJ, Van TT, Moore RJ, Stanley D. 2018. Selenium nanoparticles in poultry feed modify gut microbiota and increase abundance of Faecalibacterium prausnitzii. Appl Microbiol Biotechnol. 102(3):1455–1466.
   PubMed Web of Science ®Google Scholar
• Gao J, Lin H, Wang XJ, Song ZG, Jiao HC. 2010. Vitamin E supplementation alleviates the oxidative stress induced by dexamethasone treatment and improves meat quality in broiler chickens. Poult Sci. 89(2):318–327.
   PubMed Web of Science ®Google Scholar
• Ghazi SH, Habibian M, Moeini MM, Abdolmohammadi AR. 2012. Effects of different levels of organic and inorganic chromium on growth performance and immunocompetence of broilers under heat stress. Biol Trace Elem Res. 146(3):309–317.
   PubMed Web of Science ®Google Scholar
• Gultepe EE, Uyarlar C, Bayram I. 2018. Supplementation of cr methionine during dry period of dairy cows and its effect on some production and biochemical parameters during early lactation and on immunity of their offspring. Biol Trace Elem Res. 186(1):143–153.
   PubMed Web of Science ®Google Scholar
• Hu XF, Guo YM, Huang BY, Bun S, Zhang LB, Li JH, Liu D, Long FY, Yang X, Jiao P. 2010. The effect of glucagon-like peptide 2 injection on performance, small intestinal morphology, and nutrient transporter expression of stressed broiler chickens. Poult Sci. 89(9):1967–1974.
   PubMed Web of Science ®Google Scholar
• Jain NC. 1993. Essentials of veterinary hematology. Philadelphia (PA): Lea and Febiger. p. 222–257.
   Google Scholar
• Kececi T, Oğuz H, Kurtoğlu V, Demet O. 1998. Effects of polyvinylpolypyrrolidone, synthetic zeolite and bentonite on serum biochemical and haematological characters of broiler chickens during aflatoxicosis. Br Poult Sci. 39(3):452–458.
   PubMed Web of Science ®Google Scholar
• Korenekova B, Skalicka M, Nad P, Šály J, Korenek M. 2007. Effects of cadmium and zinc on the quality of quail's eggs. Biol Trace Elem Res. 116(1):103–109.
   PubMed Web of Science ®Google Scholar
• Lambert GP. 2009. Stress-induced gastrointestinal barrier dysfunction and its inflammatory effects. J Anim Sci. 87(14 suppl):101–108.
   PubMed Web of Science ®Google Scholar
• Li Y, Cai HY, Liu GH, Dong XL, Chang WH, Zhang S, Zheng AJ, Chen GL. 2009. Effects of stress simulated by dexamethasone on jejunal glucose transport in broilers. Poult Sci. 88(2):330–337.
   PubMed Web of Science ®Google Scholar
• Lin H, Decuypere E, Buyse J. 2004a. Oxidative stress induced by corticosterone administration in broiler chickens (Gallus gallus domesticus) 1. Chronic exposure. Comp Biochem Physiol B, Biochem Mol Biol. 139(4):737–744.
   PubMed Web of Science ®Google Scholar
• Lin H, Decuypere E, Buyse J. 2004b. Oxidative stress induced by corticosterone administration in broiler chickens (Gallus gallus domesticus) 2. Short-term effect. Comp Biochem Physiol B, Biochem Mol Biol. 139(4):745–751.
   PubMed Web of Science ®Google Scholar
• Lin H, Sui SJ, Jiao HC, Buyse J, Decuypere E. 2006. Impaired development of broiler chickens by stress mimicked by corticosterone exposure. Comp Biochem Physiol Pt A Mol Integr Physiol. 143(3):400–405.
   PubMed Web of Science ®Google Scholar
• Luo JW, Zhou ZL, Zhang H, Ma RS, Hou JF. 2013. Bone response of broiler chickens (Gallus gallus domesticus) induced by corticosterone. Comp Biochem Physiol Part A. 164(2):410–416.
   PubMed Web of Science ®Google Scholar
• Lv ZP, Peng YZ, Zhang BB, Fan H, Liu D, Guo YM. 2018. Glucose and lipid metabolism disorders in the chickens with dexamethasone‐induced oxidative stress. J Anim Physiol Anim Nutr. 102(2):e706.
   PubMed Web of Science ®Google Scholar
• Malheiros RD, Moraes VM, Collin A, Decuypere E, Buyse J. 2003. Free diet selection by broilers as influenced by dietary macronutrient ratio and corticosterone supplementation. 1. Diet selection, organ weights, and plasma metabolites. Poult Sci. 82(1):123–131.
   PubMed Web of Science ®Google Scholar
• Mumma JO, Thaxton JP, Vizzier-Thaxton Y, Dodson WL. 2006. Physiological stress in laying hens. Poult Sci. 85(4):761–769.
   PubMed Web of Science ®Google Scholar
• Muralisankar T, Bhavan PS, Radhakrishnan S, Seenivasan C, Manickam N, Srinivasan V. 2014. Dietary supplementation of zinc nanoparticles and its influence on biology, physiology and immune responses of the freshwater prawn, Macrobrachium rosenbergii. Biol Trace Elem Res. 160(1):56–66.
   PubMed Web of Science ®Google Scholar
• National Research Council. 1994. Nutrient requirements of poultry. 9th rev. ed. Washington (DC): National Academy Press.
   Google Scholar
• Nazar FN, Magnoli AP, Dalcero AM, Marin RH. 2012. Effect of feed contamination with aflatoxin B1 and administration of exogenous corticosterone on Japanese quail biochemical and immunological parameters. Poult Sci. 91(1):47–54.
   PubMed Web of Science ®Google Scholar
• Preuss HG, Grojec PL, Lieberman S, Anderson RA. 1997. Effects of different chromium compounds on blood pressure and lipid peroxidation in spontaneously hypertensive rats. Cli Neph. 47(5):325–330.
   PubMed Web of Science ®Google Scholar
• Puvadolpirod S, Thaxton JP. 2000a. Model of physiological stress in chickens 1. Response parameters. Poult Sci. 79(3):363–369.
   PubMed Web of Science ®Google Scholar
• Puvadolpirod S, Thaxton JP. 2000b. Model of physiological stress in chickens 4. Digestion and metabolism. Poult Sci. 79(3):383–390.
   PubMed Web of Science ®Google Scholar
• Ramiah SK, Awad EA, Mookiah S, Idrus Z. 2019. Effects of zinc oxide nanoparticles on growth performance and concentrations of malondialdehyde, zinc in tissues, and corticosterone in broiler chickens under heat stress conditions. Poult Sci. 98(9):3828–3838.
   PubMed Web of Science ®Google Scholar
• Sahin N, Akdemir F, Tuzcu M, Hayirli A, Smith MO, Sahin K. 2010. Effects of supplemental chromium sources and levels on performance, lipid peroxidation and proinflammatory markers in heat-stressed quails. Anim Feed Sci Technol. 159(3–4):143–149.
   Web of Science ®Google Scholar
• Sahin K, Onderci M, Sahin N, Gulcu F, Yıldız N, Avcı M, Kucuk O. 2006. Responses of quail to dietary vitamin E and zinc picolinate at different environmental temperatures. Anim Feed Sci Technol. 129(1–2):39–48.
   Web of Science ®Google Scholar
• Sahin K, Sahin N, Kucuk O. 2003. Effects of chromium, and ascorbic acid supplementation on growth, carcass traits, serum metabolites, and antioxidant status of broiler chickens reared at a high ambient temperature (32 °C). Nutr Res. 23(2):225–238.
   Web of Science ®Google Scholar
• Sahin N, Sahin K, Onderci M, Gursu MF, Cikim G, Vijaya J, Kucuk O. 2005. Chromium picolinate, rather than biotin, alleviates performance and metabolic parameters in heat-stressed quail. Br Poult Sci. 46(4):457–463.
   PubMed Web of Science ®Google Scholar
• Saleh AA, Ragab MM, Ahmed EA, Abudabos AM, Ebeid TA. 2018. Effect of dietary zinc-methionine supplementation on growth performance, nutrient utilization, antioxidative properties and immune response in broiler chickens under high ambient temperature. J Appl Anim Res. 46(1):820–827.
   Web of Science ®Google Scholar
• Siegel HS. 1995. Gordon memorial lecture. Stress, strains and resistance. Br Poult Sci. 36(1):3–22.
   PubMed Web of Science ®Google Scholar
• Sirirat N, Lu JJ, Hung AT, Chen SY, Lien TF. 2012. Effects different levels of nanoparticles chromium picolinate supplementation on growth performance, mineral retention, and immune responses in broiler chickens. J Agric Sci. 4(12):48.
   Google Scholar
• Sultana N, Amin T, Afrose M, Aqter Rony S, Rafiq K. 2020. Effects of dexamethasone on the morphometry and biometry of immune organs of broiler chicken. Int J Morphol. 38(4):1032–1038.
   Web of Science ®Google Scholar
• Sunder GS, Panda AK, Gopinath NC, Rao SR, Raju MV, Reddy MR, Kumar CV. 2008. Effects of higher levels of zinc supplementation on performance, mineral availability, and immune competence in broiler chickens. J Appl Poult Res. 17(1):79–86.
   Web of Science ®Google Scholar
• Uyanik F, Atasever A, Özdamar S, Aydin F. 2002. Effects of dietary chromium chloride supplementation on performance, some serum parameters, and immune response in broilers. Biol Trace Elem Res. 90(1-3):99–115.
   PubMed Web of Science ®Google Scholar
• Virden WS, Dozier WA, III, Corzo A, Kidd MT. 2009. Physiological stress responses in broilers as affected by drinking water supplements or dietary corn particle size. J Appl Poult Res. 18(2):244–251.
   Web of Science ®Google Scholar
• Virden WS, Kidd MT. 2009. Physiological stress in broilers: ramifications on nutrient digestibility and responses. J Appl Poult Res. 18(2):338–347.
   Web of Science ®Google Scholar
• Virden WS, Thaxton JP, Corzo A, Dozier IIW, Kidd MT. 2007. Evaluation of models using corticosterone and adrenocorticotropin to induce conditions mimicking physiological stress in commercial broilers. Poult Sci. 86(12):2485–2491.
   PubMed Web of Science ®Google Scholar
• Wall JP, Cockrem JF. 2010. Effects of corticosterone treatment in laying Japanese quail. Br Poult Sci. 51(2):278–288.
   PubMed Web of Science ®Google Scholar
• Wang MQ, Wang C, Du YJ, Li H, Tao WJ, Ye SS, He YD, Chen SY. 2014. Effects of chromium-loaded chitosan nanoparticles on growth, carcass characteristics, pork quality, and lipid metabolism in finishing pigs. Livestock Sci. 161:123–129.
   Web of Science ®Google Scholar
• Zha LY, Zeng JW, Chu XW, Mao LM, Luo HJ. 2009a. Efficacy of trivalent chromium on growth performance, carcass characteristics and tissue chromium in heat‐stressed broiler chicks. J Sci Food Agric. 89(10):1782–1786.
   Web of Science ®Google Scholar
• Zha L, Zeng J, Sun S, Deng H, Luo H, Li W. 2009b. Chromium(III) nanoparticles affect hormone and immune responses in heat-stressed rats. Biol Trace Elem Res. 129(1–3):157–169.
   PubMed Web of Science ®Google Scholar