Anchordoguy T, Crowe J H, Griffin F J, Clark W H
Department of Zoology, University of California, Davis 95616.
Cryobiology. 1988 Jun;25(3):238-43. doi: 10.1016/0011-2240(88)90031-4.
Sperm from a marine shrimp, Sicyonia ingentis, were frozen to -196 degrees C using a variety of cooling rates and cryoprotectants. A cooling rate of 1 degree C/min resulted in minimal cell breakage. Sperm samples were frozen in solutions of known membrane stabilizers--trehalose, sucrose, proline, and glycerol. These compounds were somewhat effective but a dramatic increase in sperm viability was seen when DMSO was present in the freezing medium. Sperm viability was assessed using the in vitro acrosome reaction technique of Griffin et al. (1987). The highest sperm survival (56%) was obtained with samples frozen at 1 degrees C/min in a 5% (v/v) DMSO solution. No decrease in viability was seen in sperm samples stored in liquid nitrogen (-196 degrees C) for 1 month.
使用多种降温速率和冷冻保护剂,将海洋虾类——巨型赤虾(Sicyonia ingentis)的精子冷冻至-196摄氏度。1摄氏度/分钟的降温速率导致细胞破裂最少。精子样本被冷冻于已知的膜稳定剂——海藻糖、蔗糖、脯氨酸和甘油的溶液中。这些化合物有一定效果,但当冷冻培养基中存在二甲基亚砜(DMSO)时,精子活力显著提高。使用格里芬等人(1987年)的体外顶体反应技术评估精子活力。在5%(v/v)DMSO溶液中以1摄氏度/分钟的速度冷冻的样本获得了最高的精子存活率(56%)。储存在液氮(-196摄氏度)中的精子样本在1个月内活力未见下降。