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猪新鲜精子以及添加和未添加α-生育酚冷冻保存的精子在获能条件下的蛋白质酪氨酸磷酸化

Protein tyrosine phosphorylation under capacitating conditions in porcine fresh spermatozoa and sperm cryopreserved with and without alpha tocopherol.

作者信息

Satorre M M, Breininger E, Beconi M T, Beorlegui N B

机构信息

Area of Biochemistry, School of Veterinary Sciences, University of Buenos Aires, Buenos Aires, Argentina.

出版信息

Andrologia. 2009 Jun;41(3):184-92. doi: 10.1111/j.1439-0272.2009.00915.x.

Abstract

The aim of this study was to evaluate the capacitation behaviour of fresh and alpha-tocopherol frozen spermatozoa. Spermatozoa frozen with or without alpha-tocopherol and fresh semen were incubated under capacitating conditions. Aliquots were collected at 0, 15, 30, 45, 60, 90, 120 and 180 min of incubation time. Parameters of semen quality were evaluated by optical microscopy and capacitation was determined by the epifluorescence chlortetracycline technique. Protein tyrosine phosphorylation was examined by Western immunoblotting. Motility, viability and intact spermatozoa were higher (P < 0.05) in fresh semen compared with frozen samples. These parameters significantly decreased, in every treatment, throughout the incubation time. Fresh semen showed a progressive increase in capacitated spermatozoa, reaching 25 +/- 3% at 180 min. Cryopreserved semen had a fast increase at the beginning of incubation time (28 +/- 5% at 45 min and 28 +/- 3% at 30 min for samples with or without alpha-tocopherol, respectively). The amount of an MW 32 kDa tyrosine-phosphorilated protein, associated with capacitation, increased throughout incubation for fresh semen and spermatozoa cryopreserved with alpha-tocopherol. The supplementation with alpha-tocopherol preserved sperm plasma membrane, reflected not only in the acrosome integrity but also in a greater efficiency of energy production.

摘要

本研究的目的是评估新鲜精子和经α-生育酚冷冻保存的精子的获能行为。将添加或未添加α-生育酚冷冻保存的精子以及新鲜精液在获能条件下进行孵育。在孵育时间为0、15、30、45、60、90、120和180分钟时收集等分试样。通过光学显微镜评估精液质量参数,并采用落射荧光金霉素技术测定精子获能情况。通过蛋白质免疫印迹法检测蛋白质酪氨酸磷酸化。与冷冻样本相比,新鲜精液中的精子活力、存活率和完整率更高(P<0.05)。在每种处理中,随着孵育时间的延长,这些参数均显著下降。新鲜精液中获能精子数量呈逐渐增加趋势,在180分钟时达到25±3%。冷冻保存的精液在孵育开始时快速增加(添加或未添加α-生育酚的样本在45分钟时分别为28±5%和30分钟时为28±3%)。对于新鲜精液和添加α-生育酚冷冻保存的精子,与获能相关的分子量为32 kDa的酪氨酸磷酸化蛋白的量在整个孵育过程中均增加。添加α-生育酚可保护精子质膜,这不仅体现在顶体完整性上,还体现在能量产生效率更高。

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