آمار
| تعداد نشریات | 13 |
| تعداد شمارهها | 631 |
| تعداد مقالات | 6,584 |
| تعداد مشاهده مقاله | 8,926,481 |
| تعداد دریافت فایل اصل مقاله | 8,456,793 |
Evaluation of Antioxidant Enzymes Activity, Lipid Peroxidation and Sperm Quality in Broiler Breeder Roosters Fed Whey Protein and Sodium Selenite | ||
| Poultry Science Journal | ||
| دوره 10، شماره 1، آبان 2022، صفحه 129-138 اصل مقاله (690.37 K) | ||
| نوع مقاله: Original Paper | ||
| شناسه دیجیتال (DOI): 10.22069/psj.2022.20034.1790 | ||
| نویسندگان | ||
| Mohammad Amin Namazi Zadegan؛ Hassan Kermanshahi* ؛ Ali Javadmanesh | ||
| Department of Animal Science, Faculty of Agriculture, Ferdowsi University of Mashhad, Mashhad, Iran | ||
| چکیده | ||
| The objective of this study was to investigate the effect of whey protein concentrate (WPC) and selenium (Se) supplementation on sperm quality, antioxidant enzymes activity and lipid peroxidation in seminal plasma, liver and testis of roosters. Forty-five Ross-308 broiler breeder roosters aged 60 weeks were used for an eight-week period in a 3 × 3 factorial arrangement of dietary treatments. Three levels of WPC (0.0, 1.5 and 3.0% of diet) and selenium supplementation (0.0, 0.2 and 0.4 mg/kg of diet) with five replications were tested. Total and progressive sperm motility, sperm concentration, plasma membrane integrity, and sperm viability were significantly lower in birds treated with Se supplementation-free diet (P < 0.05). Also, abnormal sperms were significantly higher in Se supplementation-free diets when compared to the diets supplemented with 0.4 mg/kg Se (P < 0.05). The use of 1.5% of WPC resulted in significantly increased total and progressive sperm motility compared to the WPC-free diet (P < 0.05). Selenium at the level of 0.4 mg/kg along with 3.0% WPC were associated with significantly increased Glutathione peroxidase and superoxide dismutase activity in seminal plasma as compared to other levels (P < 0.05). The highest level of total antioxidant capacity (TAC) in seminal plasma was observed at the level of 0.2 mg Se (P < 0.05). Further, 3.0% WPC resulted in significantly increased TAC concentration in seminal plasma compared to the WPC-free diet (P < 0.05). Moreover, the Malondialdehyde (MDA) level of seminal plasma in selenium supplementation-free diets was significantly higher than those of other levels (P < 0.05). Glutathione peroxidase activity, TAC, and MDA levels in the testis and liver were not affected by the WPC and Se levels. It can be concluded that dietary inclusion of WPC and Se improved the semen quality, increased antioxidant enzymes activity and decreased lipid peroxidation in seminal plasma of broiler breeder roosters. | ||
| کلیدواژهها | ||
| Semen quality؛ Broiler breeder rooster؛ Whey protein؛ Selenium؛ Antioxidant enzymes activity | ||
| مراجع | ||
|
Afkhami M, Kermanshahi H & Majidzadeh Heravi R. 2020. Evaluation of whey protein sources on performance, liver antioxidants and immune responses of broiler chickens challenged with ethanol. Journal of Animal Physiology and Animal Nutrition, 104: 898-908. DOI: 10.1111/jpn.13327
Ahsan U, Kamran Z, Raza I, Ahmad S, Babar W, Riaz M & Iqbal Z. 2014. Role of selenium in male reproduction—A review. Animal Reproduction Science, 146: 55-62. DOI: 10.1016/j.anireprosci.2014.01.009
Akhlaghi A, Ahangari YJ, Navidshad B, Pirsaraei ZA, Zhandi M, Deldar H, Rezvani M, Dadpasand M, Hashemi S, & Poureslami R. 2014. Improvements in semen quality, sperm fatty acids, and reproductive performance in aged Cobb 500 breeder roosters fed diets containing dried ginger rhizomes (Zingiber officinale). Poultry Science, 93: 1236-1244. DOI: 10.3382/ps.2013-03617
Allmang C & Krol A. 2006. Selenoprotein synthesis: UGA does not end the story. Biochimie, 88: 1561-1571. DOI: 10.1016/j.biochi.2006.04.015
Ashour EA, Abd El-Hack ME, Alagawany M, Swelum AA, Osman AO, Saadeldin IM, Abdel-Hamid M & Hussein E-SO. 2019. Use of whey protein concentrates in broiler diets. The Journal of Applied Poultry Research, 28: 1078-1088. DOI: 10.3382/japr/pfz070
Birben E, Sahiner UM, Sackesen C, Erzurum S & Kalayci O. 2012. Oxidative stress and antioxidant defense. World Allergy Organization Journal, 5: 9-19. DOI: 10.1097/WOX.0b013e3182439613
Bounous G. 2000. Whey protein concentrate (WPC) and glutathione modulation in cancer treatment. Anticancer Research, 20: 4785-4792. PMID: 11205219.
Bounous G & Gold P. 1991. The biological activity of undenatured dietary whey proteins: role of glutathione. Clininical and Investigative Medicine, 14: 296-309. PMID: 1782728.
Bounous G, Batist G GP, BouNoUsº G, Batist G & Gold P. 1989. Immunoenhancing property of dietary whey protein in mice: Role of glutathione. Clininical and Investigative Medicine, 12: 154-161. PMID: 2743633.
Bréque C, Surai P & Brillard JP. 2003. Roles of antioxidants on prolonged storage of avian spermatozoa in vivo and in vitro. Molecular Reproduction and Development: Incorporating Gamete Research, 66: 314-323. DOI: 10.1002/mrd.10347
Burrows W & Quinn J. 1937. The collection of spermatozoa from the domestic fowl and turkey. Poultry Science, 16: 19-24. DOI: 10.3382/ps.0160019
Cerolini S, Surai P, Maldjian A, Gliozzi T & Noble R. 1997. Lipid composition of semen in different fowl breeders. IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca, 141.
Cerolini S, Zaniboni L, Maldjian A & Gliozzi T. 2006. Effect of docosahexaenoic acid and α-tocopherol enrichment in chicken sperm on semen quality, sperm lipid composition and susceptibility to peroxidation. Theriogenology, 66: 877-886. DOI: 10.1016/ j.theriogenology. 2006.02.022
Chuaychu-Noo N, Thananurak P, Chankitisakul V & Vongpralub T. 2017. Supplementing rooster sperm with Cholesterol-Loaded-Cyclodextrin improves fertility after cryopreservation. Cryobiology, 74: 8-12. DOI: 10.1016/j.cryobiol.2016.12.012
De Wit J. 1998. Nutritional and functional characteristics of whey proteins in food products. Journal of Dairy Science, 81: 597-608. DOI: 10.3168/jds.S0022-0302(98)75613-9
Ebeid T. 2009. Organic selenium enhances the antioxidative status and quality of cockerel semen under high ambient temperature. British Poultry Science, 50: 641-647. DOI: 10.1080/00071660903303415
Edens F & Sefton A. 2009. Sel-Plex® improves spermatozoa morphology in broiler breeder males. International Journal of Poultry Science, 8: 853-861. DOI: 10.3923/ijps.2009.853.861
Fanucchi MV. 2004. Development of antioxidant and xenobiotic metabolizing enzyme systems. The Lung Development, Aging and the Environment. 177-185. DOI: 10.1016/B978-012324751-3/50046-2
Gallo R, Veronico M, Nacucchi O, Tafaro E, Barile P, Nicastro F & Zezza L. 2003. The effects of selenium, zinc and vitamin E supplementation on performance of broiler breeder males. Italian Journal of Animal Science, 2: 471-473. DOI: 10.4081/ijas.2003. 11676047
Hansen J & Deguchi Y. 1996. Selenium and fertility in animals and man–a review. Acta Veterinaria Scandinavica, 37: 19-30. DOI: 10.1186/BF03548116
Hayes A & Cribb PJ. 2008. Effect of whey protein isolate on strength, body composition and muscle hypertrophy during resistance training. Current Opinion in Clinical Nutrition & Metabolic Care, 11: 40-44. DOI: 10.1097/MCO.0b013e3282f2a57d
Jervis KM & Robaire B. 2002. Changes in gene expression during aging in the Brown Norway rat epididymis. Experimental Gerontology, 37: 897-906. DOI: 10.1016/S0531-5565(02)00024-4
John Aitken R, Clarkson JS & Fishel S. 1989. Generation of reactive oxygen species, lipid peroxidation, and human sperm function. Biology of Reproduction, 41: 183-197. DOI: 10.1095/biolreprod41.1.183
Kehr S, Malinouski M, Finney L, Vogt S, Labunskyy VM, Kasaikina MV, Carlson BA, Zhou Y, Hatfield DL & Gladyshev VN. 2009. X-ray fluorescence microscopy reveals the role of selenium in spermatogenesis. Journal of Molecular Biology, 389: 808-818. DOI: 10.1016/j.jmb.2009.04.024
Kelso K, Cerolini S, Noble R, Sparks NC & Speake B. 1996. Lipid and antioxidant changes in semen of broiler fowl from 25 to 60 weeks of age. Reproduction, 106: 201-206. DOI: 10.1530/jrf.0.1060201
Khalid A, Khudhair N, He H, Peng Z, Yaguang T & Guixue Z. 2016. Effects of dietary selenium supplementation on seminiferous tubules and SelW, GPx4, LHCGR, and ACE expression in chicken testis. Biological Trace Element Research, 173: 202-209. DOI: 10.1007/s12011-016-0646-y
Khalil-Khalili AA, Zhandi M, Zaghari M, Mehrabani-Yeganeh H, Yousefi AR & Tavakoli-Alamooti M. 2021. The effect of dietary organic selenium on reproductive performance of broiler breeder roosters under dexamethasone induced stress. Theriogenology, 161: 16-25. DOI: 10.1016/j.theriogenology. 2020.11.016
Kryukov GV, Castellano S, Novoselov SV, Lobanov AV, Zehtab O, Guigó R & Gladyshev VN. 2003. Characterization of mammalian selenoproteomes. Science, 300: 1439-1443. DOI: 10.1126/science.1083516
Lamirande ED & Gagnon C. 1993. A positive role for the superoxide anion in triggering hyperactivation and capacitation of human spermatozoa. International Journal of Andrology, 16: 21-25. DOI: 10.1111/j.1365-2605.1993.tb01148.x
Lands L, Grey V & Smountas A. 1999. Effect of supplementation with a cysteine donor on muscular performance. Journal of Applied Physiology, 87: 1381-1385. DOI: 10.1152/jappl.1999.87.4.1381
Micke P, Beeh K, Schlaak J & Buhl R. 2001. Oral supplementation with whey proteins increases plasma glutathione levels of HIV‐infected patients. European Journal of Clinical Investigation, 31: 171-178. DOI: 10.1046/j.1365-2362.2001.00781.x
Miller NJ, Rice-Evans C, Davies MJ, Gopinathan V & Milner A. 1993. A novel method for measuring antioxidant capacity and its application to monitoring the antioxidant status in premature neonates. Clinical Science, 84: 407-412. DOI: 10.1042/cs0840407
Paglia DE & Valentine WN. 1967. Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. The Journal of Laboratory and Clinical Medicine, 70: 158-169. DOI: 10.5555/uri:pii:0022214367900765
Paoletti F, Aldinucci D, Mocali A & Caparrini A. 1986. A sensitive spectrophotometric method for the determination of superoxide dismutase activity in tissue extracts. Analytical Biochemistry, 154: 536-541. DOI: 10.1016/0003-2697(86)90026-6
Partyka A, Łukaszewicz E & Niżański W. 2012. Lipid peroxidation and antioxidant enzymes activity in avian semen. Animal Reproduction Science, 134: 184-190. DOI: 10.1016/j.anireprosci.2012.07.007
Rastad A, Samiea A & Daneshvar F. 2008. Investigation of bactocell and whey powder on the performance and properties of the broiler carcass. Natural Resource and Agriculture Science and Technology, 43.
Sanocka D & Kurpisz M. 2004. Reactive oxygen species and sperm cells. Reproductive Biology and Endocrinology, 2: 1-7. DOI: 10.1186/1477-7827-2-12
Santiago-Moreno J, Castaño C, Coloma M, Gómez-Brunet A, Toledano-Díaz A, López-Sebastián A & Campo J. 2009. Use of the hypo-osmotic swelling test and aniline blue staining to improve the evaluation of seasonal sperm variation in native Spanish free-range poultry. Poultry Science, 88: 2661-2669. DOI: 10.3382/ps.2008-00542
Smith JT & Mayer DT. 1955. Evaluation of sperm concentration by the hemacytometer method: Comparison of four counting fluids. Fertility and Sterility, 6: 271-275. DOI: 10.1016/S0015-0282(16)31987-2
Sun Y, Oberley LW & Li Y. 1988. A simple method for clinical assay of superoxide dismutase. Clinical Chemistry, 34: 497-500. DOI: 10.1093/clinchem/34.3.497
Surai P, Fujihara N, Speake B, Brillard J, Wishart G & Sparks N. 2001. Polyunsaturated fatty acids, lipid peroxidation and antioxidant protection in avian semen-Review. Asian-Australasian Journal of Animal Sciences, 14: 1024-1050. DOI: 10.5713/ajas.2001.1024
Surai P, Kostjuk I, Wishart G, Macpherson A, Speake B, Noble R, Ionov I & Kutz E. 1998. Effect of vitamin E and selenium supplementation of cockerel diets on glutathione peroxidase activity and lipid peroxidation susceptibility in sperm, testes, and liver. Biological Trace Element Research, 64: 119-132. DOI: 10.1007/BF02783329
Surai PF. 2000. Organic selenium: benefits to animals and humans, a biochemist's view, Biotechnology in the Feed industry. Proc. Alltech's 16th Annual Symposium, Nottingham University Press, Pages, 205-260.
Surai PF. 2002. Natural antioxidants in avian nutrition and reproduction. Nottingham University Press Nottingham. Pages, 511-545.
Tabet F & Touyz RM. 2007. Reactive oxygen species, oxidative stress, and vascular biology in hypertension, Comprehensive Hypertension. Pages, 337-347.
Ursini F, Heim S, Kiess M, Maiorino M, Roveri A, Wissing J & Flohé L. 1999. Dual function of the selenoprotein PHGPx during sperm maturation. Science, 285: 1393-1396. DOI: 10.1126/science.285.5432.1393
Weir CP & Robaire B. 2007. Spermatozoa have decreased antioxidant enzymatic capacity and increased reactive oxygen species production during aging in the Brown Norway rat. Journal of Andrology, 28: 229-240. DOI: 10.2164/jandrol.106.001362
Wu S, Oldfield J, Whanger P & Weswig P. 1973. Effect of selenium, vitamin E, and antioxidants on testicular function in rats. Biology of Reproduction, 8: 625-629. DOI: 10.1093/biolreprod/8.5.625
Yagi K. 1976. A simple fluorometric assay for lipoperoxide in blood plasma. Biochemical Medicine, 15: 212-216. DOI: 10.1016/0006-2944(76)90049-1 | ||
|
آمار تعداد مشاهده مقاله: 676 تعداد دریافت فایل اصل مقاله: 427 |
||
سامانه مدیریت نشریات علمی. طراحی و پیاده سازی از سیناوب