تعداد نشریات | 161 |
تعداد شمارهها | 6,532 |
تعداد مقالات | 70,504 |
تعداد مشاهده مقاله | 124,123,741 |
تعداد دریافت فایل اصل مقاله | 97,231,813 |
اثر تنش اکسیداتیو ناشی از سرب بر عملکرد، وضعیت آنتیاکسیدانی و پاسخهای رفتاری جوجه های گوشتی | ||
مجله تحقیقات دامپزشکی (Journal of Veterinary Research) | ||
مقاله 12، دوره 71، شماره 4، دی 1395، صفحه 453-461 اصل مقاله (815.94 K) | ||
شناسه دیجیتال (DOI): 10.22059/jvr.2016.60002 | ||
نویسندگان | ||
روح اله ابراهیمی* 1؛ طاهره محمدآبادی1؛ محسن ساری1؛ سمیه سالاری1؛ محمدجواد ضمیری2؛ محمد تقی بیگی نصیری1 | ||
1دانشکده علوم دامی و صنایع غذایی، دانشگاه کشاورزی و منابع طبیعی رامین خوزستان، ملاثانی، خوزستان، ایران | ||
2بخش علوم دامی، دانشکده کشاورزی دانشگاه شیراز، شیراز، فارس | ||
چکیده | ||
زمینه مطالعه: تا به امروز، نمونههای بیشماری از اختلالات بیوشیمیایی، فیزیولوژیک و رفتاری ناشی از رویارویی با سرب در حیوانات گزارش شده است. از سوی دیگر، مکانیسمی که طی آن سرب موجب کاهش عملکرد پرندگان میگردد، آشکار نشده است. از اینرو، جهت بررسی این فرضیه که سرب با القای تنش اکسیداتیو و تغییر در وضعیت آنتیاکسیدانی و رفتار، بر عملکرد پرنده اثر میگذارد، این آزمایش طراحی شد. هدف: این آزمایش برای بررسی اثر تنش اکسیداتیو القا شده توسط سرب بر عملکرد، وضعیت آنتیاکسیدانی و رفتار جوجههای گوشتی انجام شد. روش کار: 80 قطعه جوجه گوشتی به طور تصادفی به دو تیمار آزمایشی با 4 تکرار (هر تکرار شامل 10 قطعه جوجه گوشتی) اختصاص یافت. جیرههای آزمایشی شامل 1) جیره پایه بدون سرب (شاهد) و 2) جیره پایه حاوی mg200 سرب در کیلوگرم جیره. نتایج: نتایج آزمایش حاضر نشان میدهد، استفاده از سرب در کل دوره پرورش، افزایش وزن روزانه را نسبت به تیمار شاهد به طور معنیداری کاهش داد (01/0>p) و موجب افزایش معنیدار ضریب تبدیل خوراک جوجههای گوشتی شد (01/0>p). همچنین، پس از مصرف جیره آلوده با محرک تنشزا، مقدار مالوندیآلدهید و نسبت هتروفیل به لنفوسیت به طور معنیداری افزایش و فعالیت آنزیم سوپراکسیددسموتاز و گلوتاتیون پراکسیداز به طور معنیداری کاهش یافت (01/0≤p). افزون بر این، استفاده از mg200 سرب در جیره موجب افزایش معنیدار وضعیت نشسته و رفتار تهاجمی و کاهش معنیدار رفتار تغذیه پرندگان شد (01/0>p). نتیجهگیری نهایی: نتایج این آزمایش نشان میدهد تنش اکسیداتیو ناشی از سرب موجب افزایش ضریب تبدیل خوراک و کاهش عملکرد پرنده میشود. از اینرو، مکانیسم پایه پیشنهادی برای بروز چنین پدیدهای این است که رویارویی با سرب از طریق اختلال در وضعیت آنتیاکسیدانی و رفتار تغذیهای پرنده موجب کاهش عملکرد میشود. | ||
کلیدواژهها | ||
تنش اکسیداتیو؛ سرب؛ وضعیت آنتیاکسیدانی؛ رفتار؛ جوجه گوشتی | ||
عنوان مقاله [English] | ||
Effect of Pb-induced oxidative stress on performance, antioxidant status and behavioral responses in broiler chicken | ||
نویسندگان [English] | ||
Rohollah Ebrahimi1؛ Tahereh mohammad abadi1؛ Mohsen Sari1؛ Somayeh Salari1؛ Mohammad Javad Zamiri2؛ Mohammad Taghi Beygi Nasiri1 | ||
1Department of Animal Science, Faculty of Agriculture Science, Ramin Agriculture and Natural Resources University of Khuzestan, Khuzestan, Iran | ||
2Department of Animal Science, Shiraz University, Fars, Iran | ||
چکیده [English] | ||
BACKGROUND: Lead (Pb) induced oxidative stress is known to suppress growth performance in broiler chickens. The current study was carried out in an attempt to describe the specific underlying mechanisms of such phenomenon. OBJECTIVES: The objective of this study was to investigate the effect of Pb-induced oxidative stress on performance, antioxidant status and behavioral responses of broiler chicken. METHODS: Eighty day-old broiler chicks were randomly assigned to 2 dietary treatment groups of 4 pen replicates, namely i) basal diet containing no lead supplement (control) and ii) basal diet containing 200 mg Pb/kg of diet. RESULTS: The results showed that addition of lead decreased body weight gain (p<0.01) and feed conversion ratio (p<0.01). Also, consumption of contaminated diet significantly increased MDA and H/L Ratio and significantly decreased SOD and GPx activity (p<0.01). Moreover, addition of 200 mg/kg diet significantly increased sitting pasture and aggression behavior and decreased feeding behavior (p<0.01). CONCLUSIONS: Our data conclude that Pb-induced oxidative stress adversely suppressed feed conversion ratio and growth performance. The proposed underlying mechanism for such phenomenon is Pb-induced oxidative stress by impaired antioxidant status and feeding behavior decreased the growth performance. | ||
کلیدواژهها [English] | ||
oxidative stress, lead, antioxidant status, Behavior, broiler | ||
مراجع | ||
Ahamed, M., Siddiqui, M.K.J. (2007) Low levels lead exposure and oxidative stress: Current opinions. Clinica Chimica Acta. 383: 57-64.
Bakalli, R.I., Pesti, G.M., Ragland, W.L. (1995) The magnitude of lead toxicity in broiler chickens. Vet Hum Toxicol. 37: 15-19.
Bayram, A., Özkan, S. (2010) Effects of a 16-hour light, 8-hour dark lighting schedule on behavioral traits and performance in male broiler chickens. J Appl Poult Res. 19: 263-273.
Bendich, A. (1993) Physiological role of antioxidants in the immune system. J Dairy Sci. 76: 2789-2794.
Buege, J., Aust, S. (1978) Microsomal lipid peroxidation. Meth Enzymol. 52: 302-306.
Burkholder, K., Thompson, M.K.L., Einstein, M.E., Applegate, T.J., Patterson, J.A. (2008) Influence of Stressors on Normal Intestinal Microbiota, Intestinal Morphology, and Susceptibility to Salmonella Enteritidis Colonization in Broilers. Poult Sci. 87: 1734-1741.
Cabib, S. (2007) The neurobiology of stereotypy II: The role of stress stereotypic. In: Stereotypic Animal Behavior: Fundamentals and Applications to Welfare. Mason, G., Rushen, J. (eds.). Wallingford, CAB International, UK. p. 227-255.
Canfield, R.L., Henderson, C.R.J., Cory-Slechta, D.A., Cox, C., Jusko, T.A., Lanphear, B.P. (2003) Intellectual impairment in children with blood lead concentrations below10 microgram per deciliter. N Engl J Med. 348: 1517-26.
Chang, W., Chen, J.,Wei, Q.Y., Chen, X.M. (2006) Effects of Brn-3a protein and RNA expression in rat brain following low-level lead exposure during development on spatial learning and memory. Toxicol Lett. 164: 63-70.
Chiodo, L.M., Jacobson, S.W., Jacobson, J.L. (2004) Neurodevelopmental effects ofpostnatal lead exposure at very low levels. Neurotoxicol Teratol. 26: 359-71.
Cory-Slechta, D.A., Virgolini, M.B., Thiruchelvam, M., Weston, D.D., Bauter, M.R. (2004) Maternal stress modulates effects of developmental lead exposure. Environ. Health Perspect. 112: 717-730.
Courtois, E., Marques, M., Barrientos, A. (2003) Lead-induced down-regulation of soluble guanylate cyclase in isolated rat aortic segments mediated by reactive oxygen species and cyclo-oxygenase-2. J Am Soc Nephrol. 14: 1464-70.
Dameron, B.L., Simpson, C.F., Harms, R.H. (1969) The effect of feeding various levels of lead on the performance of broilers. Poult Sci. 48: 1507-1509.
Dickey, E.R., Bregendahl, K., Stalder, K., Fitzgerald, R., Johnson, A.K. (2010) Effects of a premolt calcium and low-energy molt program on laying hen behavior and heterophil-to-lymphocyte ratios. Poult Sci. 89: 2317-2325.
Dong, H., Lin, H., Jiao, H.C., Song, Z.G., Zhao, J.P., Jiang, K.J. (2007) Altered development and protein metabolism inskeletal muscles of broiler chickens (Gallus gallus domesticus) by corticosterone. Comp Biochem Physiol. 147: 189-195.
Liang, D.X., Edelstein, D., Rossetti, L., Fantus, I.G., Goldberg, H. Ziyadeh, F., Wu, J., Brownlee, M. (2000) Hyperglycemia-induced mitochondrial superoxide overproduction activates the hexosamine pathway and induces plasminogen activator inhibitor-1 expression by increasing Sp1 glycosylation. Proc Natl Acad Sci. USA. 97: 12222-12226.
Edens, F.W., Garlich, J.D. (1983) Lead-induced egg production decrease in leghorn and Japanese quail hens. Poult Sci. 62: 1757-1763.
Ercal, N., Guerer-Orhan, H., Aykin-Burns, N. (2001) Toxic metals and oxidative stress part I: mechanisms involved in metal induced oxidative damage. Curr Top in med Chem. 1: 529-539.
Erdogan, Z., Erdogan, S., Celik, S., Unlu, A. (2005) Effects of ascorbic acid on cadmium-induced oxidative stress and performance of broilers. Biol Trace Elem Res. 104: 19-32.
Franco, R., Sanchez-Olea, R., Reyes-Reyes, E.M., Panayiotidis, M.I. (2009) Environmental toxicity, oxidative stress and apoptosis: Menage a Trois Mutat Res. 674: 3-22.
Garriga, C., Hunter, R.R., Amat, C., Planas, J.M., Mitchell, M.A., Moreto, M. (2006) Heat stress increases apical glucose transport in the chicken jejunum. Am J Physiol Regul Integr Comp Physiol. 290: 195-201.
Gilgun-Sherki, Y., Melamed, E., Offen, D. (2001) Oxidative stress induced-neurodegenerative diseases: the need for antioxidants that penetrate the blood brain barrier. Neuropharmacol. (Review) 40: 959-75.
Gochfeld, M., Burger, J. (1988) Effects of Lead on Growth and Feeding Behavior of Young Common Terns (Sterna hirundo). Arch Environ Contam Toxicol. 17: 513-517.
Golter, M., Michaelson, I.A. (1975) Growth, behavior, and brain catecholamines in lead-exposed neonatal rats: A Reappraisal Science. 187: 359-61.
Haider, S., Saleem, S., Tabassum, S., Khaliq, S., Shamim, S., Batool, Z., Parveen, T., Inam, Q., Haleem, D.J. (2013) Alteration in plasma corticosterone levels following long term oral administration of lead produces depression like symptoms in rats. Metab Brain Dis. 28: 85-92.
Hamilton, J.D., O’Flaherty, E.J. (1995) Influence of lead on mineralization during bone growth. Fundament. App Toxicol. 26: 265-271.
Hsu, PC., Guo, YL. (2002) Antioxidant nutrients and lead toxicity. Toxicol. 180: 33-44.
Hu, X.F., Guo, Y.M., Huang, B.Y., Bun, S., Zhang, L.B., Li, J.H., Liu, D., Long, F.Y., 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: 1967-1974.
Levine, S., Ursin, H. (1991) What is stress? In: Stress: Neurobiology and Neuroendocrinology. Brown, M.R., Koob, G.F., Rivier, C. (eds.). Marcel Dekker, Inc, New York. p. 3-21.
Liu, C.M., Ma, J.Q., Sun, Y.Z. (2012) Puerarin protects the rat liver against oxidative stress-mediated DNA damage and apoptosis induced by lead. Exp Toxicol Pathol. 64: 575- 582.
Maboeta, M.S.M., Reinecke, A.J.M., Reinecke, S.A. (1999) Effects of low levels of lead on growth and reproduction of the asian earthworm perionyx excavatus (Oligochaeta). Ecotox Environ Safe. 44: 236-240.
Mahesar, S.A., Sherazi, S.T.H., Niaz, A., Bhanger, M.I., Abdul Rauf, S. (2010) Simultaneous assessment of zinc, cadmium, lead and copper in poultry feeds by differential pulse anodic stripping voltammetry. Food Chem Toxicol. 48: 2357-2360.
Mateo, R., Nelson Beyer, W., Spann, J., Hoffman, D., Ramis, A. (2003) Relationship Between Oxidative Stress, Pathology, and Behavioral Signs of Lead Poisoning in Mallards. J Toxicol Environ Health. Part A. 66: 1371-1389.
Michaelson, M., Sauerhoff, W. (1974) An improved model of lead-induced brain dysfunction in the suckling rat. Toxicol Appl Pharmacol. 28: 88-96.
National Research Council. (1994) Nutrient Requirements of Poultry. (9th ed.) Natl Acad. Washington, DC, USA.
Newairy, A.A., Abdou, H.M. (2009) Protective role of flax lignans against lead acetate induced oxidative damage and hyperlipidemia in rats. Food Chem Toxicol. 47: 813-818.
Paglia, D.E., Valentine, W.N. (1967) Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. J Lab Clinic Med. 70: 158-169.
Robin, M.A., Prabu, S.K., Raza, H., Anandatheerathavarada, H.K., Avadhani, N.G. (2003) Phosphorylation enhances mitochondrial targeting of GSTA4-4 through increased affinity for binding to cytoplasmic Hsp70. J Biol Chem. 278: 18960-18970.
Sargent, J.R., McEvoy, L.A., Bell, J.G. (1997) Requirements, presentation and sources of polyunsaturated fatty acids in marine fish larval feeds. Aquaculture. 155: 117-127.
Seven, I., Taylan, A., Pınar, T. (2012) The effects of propolis and vitamin C supplemented feed on performance, nutrient utilization and carcass characteristics in broilers exposed to lead. Livest Sci. 148: 10-15.
Shafiq-ur-Rehman. (1991) Effects of lead on the behavioral complex stereotypes and regional dopamine levels in rats. Arch Environ Contam Toxicol. 20: 527-530.
Shields, S.J., Garner, J.P., Mench, J.A. (2005) Effect of Sand and Wood-Shavings Bedding on the Behavior of Broiler Chickens. Poult Sci. 84: 1816-1824.
Sun S.W, Yu, H.Q., Zhang, H., Zheng, Y.L., Wang J.J., Luo, L. (2007) Quercetin attenuates spontaneous behavior and spatial memory impairment in d-galactose-treated mice by increasing brain antioxidant capacity. Nutr Res. 27: 169-175.
Warren, M.J., Cooper, J.B., Wood, S.P., Shoolingin-Jordan, P.M. (1998) Lead poisoning, haem synthesis and 5-aminolaevulinic acid dehydratase. Trends Biochem Sci. 23: 217-221.
Woolliams, J.A., Wiener, G., Anderson, P.H., Mcmurray, C.H. (1983) Variation in the activities of glutathione-peroxidase and superoxide-dismutase and in the concentration of copper in the blood in various breed crosses of sheep. Res Vet Sci. 34: 253-256.
Xiang, J.J., Zhai, Y.F., Tang, Y., Wang, H., Liu, B., Guo, C.W. (2010) A competitive indirect enzyme-linked immunoassay for lead ion measurement using MABS against the lead-DTPA complex. Environ Poult. 158: 1376-1380.
Xu, J., Lian, L., Wu, C., Wang, X., Fu, W., Xu, L. (2008) Lead induces oxidative stress, DNA damage and alteration of p53, Bax and Bcl-2 expressions in mice. Food Chem Toxicol. 46: 1488-1494.
Zalups, R.K., Koropatnick, J. (2010) Cellular and Molecular Biology of Metals. CRC Press. Taylor and Francis Group. 6000 Broken Sound Parkway NW, Suite 300 Boca Raton, FL, 33487-2742.
Zulkifli, M.T., Norma, C., Chong, C.H., Loh, T.C. (2000) Heterophil to lymphocyte ratio and tonic immobility reactions to preslaughter handling in broiler chickens treated with ascorbic acid. Poult Sci. 79: 402-406 | ||
آمار تعداد مشاهده مقاله: 1,154 تعداد دریافت فایل اصل مقاله: 1,192 |