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添加剂、抗冻剂和冷冻保存方法对鲤鱼(Cyprinus carpio)精子的影响。

The effect of extenders, cryoprotectants and cryopreservation methods on common carp (Cyprinus carpio) sperm.

机构信息

Department of Aquatic Science, Faculty of Science, Burapha University, Bangsaen, Chonburi 20131, Thailand.

出版信息

Anim Reprod Sci. 2010 Dec;122(3-4):236-43. doi: 10.1016/j.anireprosci.2010.08.017. Epub 2010 Aug 26.

Abstract

The objective of this study was to determine the effects of various extenders, cryoprotectants and cryopreservation methods on post-thaw sperm motility and duration of sperm motility in common carp (Cyprinus carpio). We focused on freezing of common carp sperm utilizing a practical and inexpensive protocol for aquaculture. Sperm were diluted 1:1 in one of six extenders (common carp sperm extenders; CCSE 1-CCSE 6) containing three types of cryoprotectants (dimethyl sulfoxide; DMSO, methanol; MET and propylene glycol; PG) at a final concentration of 10%, and frozen at a rate of 10°C/min from an initial temperature 25 to -40°C before storage in liquid nitrogen. The results demonstrated that sperm diluted with CCSE 2 and DMSO had the best post-thaw motility (94.5 ± 3.3%), similar to that of the control (98.6 ± 0.7%; P>0.05). Duration of sperm motility from a treatment with CCSE 2 and DMSO (97 ± 20.8s) was not significantly different (P>0.05) from that of the control (73.3 ± 12.9s). A second experiment studied the effects of various cryopreservation methods on post-thaw sperm motility and duration of sperm motility, based on using CCSE 2 and DMSO in all treatments. Sperm were frozen using different cryopreservation methods: direct immersion into liquid nitrogen, controlled-rate programmable freezer, or exposure to liquid nitrogen vapor at different heights and time. Sperm frozen at a height of 2 cm above liquid nirogen surface for 10 min gave the highest post-thaw sperm motility (91.7 ± 7.8%) and longest duration of post-thaw sperm motility (105.7 ± 23.1s). Sperm frozen 2 cm above liquid nitrogen surface for 10 min produced the highest fertilization and hatching rate of about 73.6 ± 6.5% and 62.8 ± 5.9%, respectively, not significant different (P>0.05) from those of fresh sperm (75.6 ± 7.5% and 66.5 ± 4.8%, respectively). This study reports superior performance of the combination of CCSE 2 and DMSO for freezing common carp sperm that resulted in high fertilization capacity.

摘要

本研究旨在确定不同的 extender、cryoprotectants 和 cryopreservation 方法对鲤鱼(Cyprinus carpio)精子解冻后活力和活力持续时间的影响。我们专注于利用一种实用且廉价的水产养殖方案来冷冻鲤鱼精子。精子在六种 extender(CCSE1-CCSE6)之一中以 1:1 的比例稀释,每种 extender 均含有三种 cryoprotectants(dimethyl sulfoxide;DMSO、methanol;MET 和 propylene glycol;PG),终浓度为 10%,从初始温度 25°C 以 10°C/min 的速率降温至-40°C,然后在液氮中储存。结果表明,用 CCSE2 和 DMSO 稀释的精子解冻后活力最佳(94.5 ± 3.3%),与对照组(98.6 ± 0.7%;P>0.05)相似。用 CCSE2 和 DMSO 处理的精子活力持续时间(97 ± 20.8s)与对照组(73.3 ± 12.9s)无显著差异(P>0.05)。第二项实验基于所有处理均使用 CCSE2 和 DMSO,研究了不同 cryopreservation 方法对解冻后精子活力和活力持续时间的影响。精子采用不同的 cryopreservation 方法冷冻:直接浸入液氮中、可编程控速冷冻机或在不同高度和时间下暴露于液氮蒸气中。将精子在距液氮表面 2cm 处冷冻 10min,可获得最高的解冻后精子活力(91.7 ± 7.8%)和最长的解冻后精子活力持续时间(105.7 ± 23.1s)。将精子在距液氮表面 2cm 处冷冻 10min,可获得最高的受精率和孵化率,分别约为 73.6 ± 6.5%和 62.8 ± 5.9%,与新鲜精子(分别为 75.6 ± 7.5%和 66.5 ± 4.8%)无显著差异(P>0.05)。本研究报告了 CCSE2 和 DMSO 联合用于冷冻鲤鱼精子的优异性能,可获得高受精能力。

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