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Cryopreservation of sperm in marine fish

机译:海水鱼类精子的冷冻保存

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Since the first work of Blaxter in 1953, fish sperm cryopreservation has been attempted on about 30 marine species. The present paper reviews the techniques used and the results published in these species. Particular attention is paid to the handling procedure of sperm before freezing, the problems of semen ageing and semen contamination with urine. The quality of frozen-thawed semen was evaluated using previously standardized biotests, such as a two-step motility activation technique adapted for the different species and fertilization assays using a discriminating insemination technique. Most extenders used in marine fish are saline or sugar solutions. From the investigated cryoprotectants, dimethyl sulphoxide (DMSO) generally leads to the best results. Cooling rates range from 8 deg C to 99 deg C min~-1; the thawing rate is generally high, Compared with freshwater species, a high percentage of spermatozoa survives cryopreservation. Therefore, and because of the simplicity of the techniques, thecryopreservation of marine fish sperm is suited for application in aquaculture.
机译:自1953年进行Blaxter的首次研究以来,已经尝试对约30种海洋物种进行鱼精子冷冻保存。本文概述了使用的技术以及在这些物种中发表的结果。要特别注意冷冻前精子的处理程序,精液老化和精液被尿液污染的问题。使用先前标准化的生物测试(例如适用于不同物种的两步动力激活技术和使用区分授精技术的受精测定)评估冷冻解冻精液的质量。海鱼中使用的大多数增量剂是盐溶液或糖溶液。从研究的防冻剂来看,二甲亚砜(DMSO)通常可带来最佳效果。冷却速率范围从8摄氏度到99摄氏度min〜-1;融化率通常很高。与淡水物种相比,冷冻保存的精子比例高。因此,并且由于技术的简单性,海水鱼精子的低温保存适合用于水产养殖。

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