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血小板激活因子对新鲜及冷冻保存的公猪精子活力、质膜完整性、获能过程和顶体反应的影响。

Effect of platelet-activating factor on motility, plasmalemma integrity, the process of capacitation and acrosome reaction of fresh and cryopreserved boar spermatozoa.

作者信息

Kordan W, Lecewicz M, Tobolski J

机构信息

Department of Animal Biochemistry and Biotechnology, University of Warmia and Mazury in Olsztyn, Oczapowskiego 5, 10-719 Olsztyn-Kortowo, Poland.

出版信息

Pol J Vet Sci. 2009;12(2):175-81.

Abstract

The aim of the present study was to establish the effects of platelet-activating factor (PAF) on selected movement parameters, plasmalemma integrity, capacitation process and acrosome reaction in cryopreserved boar spermatozoa. A positive effect of PAF addition to cryopreserved semen on sperm motility was demonstrated, particularly with the application of phospholipid concentration of 1 x 10(-6)M-1 x 10(-5)M. A moderate induction of plasmalemma damage of cryopreserved spermatozoa was observed when PAF was used at a low concentration (1 x 10(-8)M-1 x 10(-7)M). The rate at which PAF induced the process of capacitation was inversely proportional to its concentration in the sample (the highest for the concentration of 1 x 10(-8)M, and the lowest at 1 x 10(-5)M). In turn, the strongest induction of acrosome reaction of spermatozoa was observed in samples with the addition of PAF at a concentration of 1 x 10(-7)M. The results obtained suggest that the application of PAF supplement to post-thawed boar semen can be used as a laboratory test of the ability of spermatozoa to induce the acrosome reaction.

摘要

本研究的目的是确定血小板活化因子(PAF)对冷冻保存的公猪精子的选定运动参数、质膜完整性、获能过程和顶体反应的影响。已证明向冷冻保存的精液中添加PAF对精子活力有积极作用,尤其是在磷脂浓度为1×10⁻⁶M - 1×10⁻⁵M时。当以低浓度(1×10⁻⁸M - 1×10⁻⁷M)使用PAF时,观察到冷冻保存的精子质膜损伤有适度诱导。PAF诱导获能过程的速率与其在样品中的浓度成反比(浓度为1×10⁻⁸M时最高,1×10⁻⁵M时最低)。反过来,在添加浓度为1×10⁻⁷M的PAF的样品中观察到精子顶体反应的最强诱导。所得结果表明,向解冻后的公猪精液中添加PAF补充剂可作为精子诱导顶体反应能力的实验室测试。

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