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精浆成分可以在冷冻保存过程中保护鲤鱼精子。

Seminal plasma fractions can protect common carp (Cyprinus carpio) sperm during cryopreservation.

机构信息

University of South Bohemia in Ceske Budejovice, Faculty of Fisheries and Protection of Waters, South Bohemian Research Center of Aquaculture and Biodiversity of Hydrocenoses, Research Institute of Fish Culture and Hydrobiology, Zátiší 728/II, 389 25, Vodňany, Czech Republic.

Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, No. 189 Songling Road, Qingdao, 266101, China.

出版信息

Fish Physiol Biochem. 2020 Aug;46(4):1461-1468. doi: 10.1007/s10695-020-00805-9. Epub 2020 May 19.

Abstract

This study aimed to investigate the effect of fractionated seminal plasma on characteristics of common carp Cyprinus carpio cryopreserved sperm. Nanosep® centrifugal devices yielded four seminal plasma fractions with different total protein content ranging in molecular weight from less than 17 to almost 74 kDa. Each protein fraction was added to semen extender medium prior to freezing. Spermatozoon motility characteristics and DNA integrity were analyzed in supplemented and non-supplemented cryopreserved samples. The cryopreservation process strongly affected the swim-up sperm quality. Treatment with fractions 1, 2, 3, and 4 was associated with significantly higher spermatozoon motility rate and curvilinear velocity than seen in extender only, with highest values obtained with fraction 4 (78.21 ± 2.41% and 168.05 ± 4.46 μm/s, respectively). Significantly less DNA damage, expressed as percent tail DNA (12.23 ± 1.27) and olive tail moment (0.68 ± 0.12), was recorded in fraction 4. The findings indicated that addition of fractionated seminal plasma to cryopreservation medium can preserve the quality of common carp sperm. The protective effect of each fraction varied, suggesting the presence of distinct components exerting different effects on cryopreserved sperm function.

摘要

本研究旨在探讨分段精液对鲤鱼冷冻精子特性的影响。Nanosep®离心设备产生了四种不同总蛋白含量的精液成分,分子量范围从小于 17 到近 74 kDa。在冷冻前,将每个蛋白质成分添加到精液稀释液中。分析了补充和未补充冷冻样本中精子运动特性和 DNA 完整性。冷冻过程强烈影响了泳动精子的质量。与仅用稀释液处理相比,处理 1、2、3 和 4 组分与显著更高的精子运动率和曲线速度相关,其中 4 组分的效果最佳(78.21±2.41%和 168.05±4.46 μm/s)。在 4 组分中记录到的 DNA 损伤明显较少,表现为尾部 DNA 百分比(12.23±1.27)和橄榄尾矩(0.68±0.12)。研究结果表明,将分段精液添加到冷冻保存介质中可以保持鲤鱼精子的质量。每个部分的保护作用不同,表明存在不同的成分对冷冻精子功能产生不同的影响。

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