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Spermatozoa and seminal plasma fatty acids as predictors of cryopreservation success

机译:精子和精浆中的脂肪酸可作为冷冻保存成功的指标

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摘要

There is a lack of information about the importance of fatty acid composition of the human sperm membranes and seminal plasma in the cryopreservation procedure. Our aims were to study the possible relationships between the fatty acid composition of human spermatozoa or seminal fluid before freezing, and the sperm quality, measured in terms of viability and motility, before and after freezingthawing. A further objective of this study was to determine whether the antioxidant capacity (TAC) of the seminal plasma is related to fatty acid (FA) composition and to success of the cryopreservation process. Polyunsaturated fatty acids (PUFA), 3 PUFAs and docosahexaenoic acid (DHA) in spermatozoa were significantly positively correlated with sperm viability and motility parameters before and after freezing. An inverse relationship was found for monounsaturated (MUFA), ratio 6/3, ratio saturated saturated fatty acids/PUFA (SFA/PUFA) with the seminal parameters. Seminal plasma fatty acid composition was not related to viability. However, motility parameters before and after freezing were related to stearic acid (C18:0) and DHA. TAC in seminal plasma was directly related to PUFA, w3 and DHA. On the other hand, SFA, C22:0, C24:0 and MUFA in seminal plasma were inversely related to the antioxidant capacity. TAC was directly correlated with motion parameters after thawing, We described a significant correlation between the fatty acid composition of the human spermatozoa or seminal plasma and the sperm parameters of the samples after thawing. PUFA, W3 and specially DHA are directly correlated with sperm motility and viability after freezing/thawing, and MUFA was inversely correlated. This means that in the future the fatty acid composition could be used as a predictor of the capacity of cryopreservation. On the other hand, we could design further procedures to modify the lipid composition or/and antioxidant capacity of ejaculate to make it more resistant to the cryopreservation process.
机译:缺乏关于冷冻保存过程中人精子膜和精浆脂肪酸组成的重要性的信息。我们的目标是研究冷冻前和冷冻后人类精子或精液的脂肪酸组成与精子质量之间的可能关系,精子质量以活力和运动性衡量。这项研究的另一个目的是确定精浆的抗氧化能力(TAC)是否与脂肪酸(FA)的组成以及冷冻保存过程的成功有关。冷冻前后精子中的多不饱和脂肪酸(PUFA),3种PUFA和二十二碳六烯酸(DHA)与精子的活力和活力参数显着正相关。发现单不饱和度(MUFA),比率6/3,饱和饱和脂肪酸/ PUFA(SFA / PUFA)的比率与主要参数成反比关系。精浆血浆脂肪酸组成与生存能力无关。然而,冷冻前后的运动参数与硬脂酸(C18:0)和DHA有关。精浆中的TAC与PUFA,w3和DHA直接相关。另一方面,精浆中的SFA,C22:0,C24:0和MUFA与抗氧化能力成反比。 TAC与融化后的运动参数直接相关。我们描述了人类精子或精浆的脂肪酸组成与融化后样品的精子参数之间的显着相关性。 PUFA,W3和特别是DHA与冷冻/解冻后的精子活力和生存力直接相关,而MUFA与之相反。这意味着将来脂肪酸组合物可以用作冷冻保存能力的预测指标。另一方面,我们可以设计进一步的程序来改变射精的脂质组成或/和抗氧化剂的能力,使其对冷冻保存过程更具抵抗力。

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