Department of Aquatic Science, Faculty of Science, Burapha University, Bangsaen, Chonburi 20131, Thailand.
Anim Reprod Sci. 2010 Dec;122(3-4):236-43. doi: 10.1016/j.anireprosci.2010.08.017. Epub 2010 Aug 26.
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.
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。