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首页> 外文期刊>Animal Reproduction Science >Under-nutrition reduces spermatogenic efficiency and sperm velocity, and increases sperm DNA damage in sexually mature male sheep
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Under-nutrition reduces spermatogenic efficiency and sperm velocity, and increases sperm DNA damage in sexually mature male sheep

机译:营养不足会降低性成熟雄性绵羊的生精效率和精子速度,并增加精子DNA的损伤。

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We tested whether the quality of spermatozoa from mature male sheep would be affected during nutrition-induced changes in testicular mass. Merino rams were fed for 65 days with diets that increased, maintained or decreased body and testis mass (n = 8 per group). In semen collected on Days 56 and 63, underfed rams had less sperms per ejaculate than wellfed rams (P < 0.05) and a lower sperm velocity (computer-assisted semen analysis) than well-fed or maintenance-fed rams (P < 0.05). Sperm chromatin structure assay revealed more sperm DNA damage in underfed rams than in well-fed rams (P < 0.05). The amount of sperm DNA damage was inversely correlated with change in scrotal circumference (r= -0.6, P < 0.05), the percentages of progressive motile sperm (r= -0.8; P < 0.01) and motile sperm (r = -0.6, P < 0.05), and the numbers of sperms per gram of testis (r= -0.55, P < 0.05). In testicular tissue collected on Day 65, underfed rams had fewer sperm per gram of testis than rams in the other two groups (P < 0.001). We conclude that, in adult rams, underfeeding reduces spermatogenic efficiency and that this response is associated with a reduction in spermatozoal quality. (C) 2014 Elsevier B.V. All rights reserved.C1 [Guan, Yongjuan; Malecki, Irek A.; Hawken, Penelope A. R.; Martin, Graeme B.] Univ Western Australia, UWA Inst Agr M082, Crawley, WA 6009, Australia. [Guan, Yongjuan; Malecki, Irek A.; Hawken, Penelope A. R.; Martin, Graeme B.] Univ Western Australia, Sch Anim Biol M082, Crawley, WA 6009, Australia. [Malecki, Irek A.] Univ Stellenbosch, Dept Anim Sci, ZA-7600 Matieland, South Africa. [Linden, Matthew D.] Univ Western Australia, Ctr Microscopy Characterisat & Anal, Perth, WA 6009, Australia. [Martin, Graeme B.] Univ Oxford, Nuffield Dept Obstet & Gynaecol, Oxford OX3 9DU, England.RP Martin, GB (reprint author), Univ Western Australia, Sch Anim Biol M085, 35 Stirling Highway, Crawley, WA 6009, Australia.EM graeme.martin@uwa.edu.auRI Martin, Graeme/A-2618-2008OI Martin, Graeme/0000-0002-1905-7934FU UWA School of Animal Biology and Yongjuan Guan; University of Western AustraliaFX This project was funded by the UWA School of Animal Biology and Yongjuan Guan was financially supported by a Scholarship for International Research Fees from the University of Western Australia. The authors are very grateful to Dr John Milton (School of Animal Biology, University of Western Australia) for designing the nutrition treatments. For assistance in handling the animals, we thank Mr. Matt Wilmot (CSIRO, Perth, Western Australia), Dr. Cesar Rosales Nieto and Mr. Gary Cass (School of Animal Biology, University of Western Australia). We would like to thank Dr. Anne Jequier (Pivet Medical, Perth, Western Australia) for her guidance on techniques, and Mr. Sheng Zhang (Zhejiang University, China), Ms. Margaret Blackberry, Dr. Trina Jorre de St Jorre and Mr. Fahad Almohsen (School of Animal Biology, University of Western Australia) for help with the collection and preservation of tissue.NR 50
机译:我们测试了在营养诱导的睾丸质量变化过程中,成年雄性绵羊精子的质量是否会受到影响。美利奴羊公羊饲喂增加,维持或减少身体和睾丸质量的饲料65天(每组n = 8)。在第56天和第63天收集的精液中,精料不足的公羊每次射精的精子数量少于精良的公羊(P <0.05),精子的速度(计算机辅助精液分析)低于精料或维持性公羊的精子速度(P <0.05) 。精子染色质结构测定显示,饲喂不足的公羊比精饲的公羊有更多的精子DNA损伤(P <0.05)。精子DNA损伤的量与阴囊周长的变化呈负相关(r = -0.6,P <0.05),进行性活动精子的百分比(r = -0.8; P <0.01)和活动精子的百分比(r = -0.6, P <0.05),以及每克睾丸的精子数量(r = -0.55,P <0.05)。在第65天收集的睾丸组织中,每克睾丸供精不足的公羊比其他两组公羊的精子少(P <0.001)。我们得出的结论是,在成年公羊中,饲喂不足会降低生精效率,而且这种反应与精子质量下降有关。 (C)2014 Elsevier B.V.保留所有权利。C1[Guan,Yongjuan; Malecki,Irek A .;霍肯,佩内洛普A. R .; Martin,GraemeB。]西澳大利亚大学,UWA Inst Agr M082,Crawley,WA 6009,澳大利亚。 [关永娟; Malecki,Irek A .;霍肯,佩内洛普A. R .; Martin,Graeme B.] Univ Western Australia,Sch Anim Biol M082,Crawley,WA 6009,澳大利亚。 [Malecki,Irek A.] Univ Stellenbosch,动物科学部门,ZA-7600 Matieland,南非。 [Linden,Matthew D.]西澳大利亚大学,Ctr Microscopy Characterisat&Anal,澳大利亚珀斯,西澳大利亚州6009。 [Martin,Graeme B.] Univ Oxford,Nuffield Dept Obstet&Gynaecol,Oxford OX3 9DU,England.RP Martin,GB(转载作者),Univ Western Australia,Sch Anim Biol M085,35 Stirling Highway,Crawley,WA 6009,澳大利亚EM graeme.martin@uwa.edu.au RI Martin,Graeme / A-2618-2008OI Martin,Graeme / 0000-0002-1905-7934FU西澳大学动物生物学学院和关永娟;西澳大利亚大学FX该项目由西澳大学动物生物学学院资助,关永娟获得西澳大利亚大学国际研究费奖学金的资助。作者非常感谢John Milton博士(西澳大利亚大学动物生物学学院)设计营养治疗方法。对于处理动物方面的帮助,我们感谢Matt Wilmot先生(CSIRO,西澳大利亚州珀斯),Cesar Rosales Nieto博士和Gary Cass先生(西澳大利亚大学动物生物学学院)。我们要感谢Anne Jequier博士(西澳大利亚珀斯的Pivet Medical)对技术的指导,以及Zhang Zhang先生(中国浙江大学),Margaret Blackberry女士,Trina Jorre de St Jorre博士和Mr. 。Fahad Almohsen(西澳大利亚大学动物生物学学院)在组织收集和保存方面的帮助NR 50

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