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1 型大麻素受体通过损害碳酸氢盐对获能公猪精子的激活作用来降低其膜流动性。

Type-1 cannabinoid receptors reduce membrane fluidity of capacitated boar sperm by impairing their activation by bicarbonate.

机构信息

Department of Biomedical Comparative Sciences, University of Teramo, Teramo, Italy.

出版信息

PLoS One. 2011;6(8):e23038. doi: 10.1371/journal.pone.0023038. Epub 2011 Aug 4.

Abstract

BACKGROUND

Mammalian spermatozoa acquire their full fertilizing ability (so called capacitation) within the female genital tract, where they are progressively exposed to inverse gradients of inhibiting and stimulating molecules.

METHODOLOGY/PRINCIPAL FINDINGS: In the present research, the effect on this process of anandamide, an endocannabinoid that can either activate or inhibit cannabinoid receptors depending on its concentration, and bicarbonate, an oviductal activatory molecule, was assessed, in order to study the role exerted by the type 1 cannabinoid receptor (CB1R) in the process of lipid membrane remodeling crucial to complete capacitation. To this aim, boar sperm were incubated in vitro under capacitating conditions (stimulated by bicarbonate) in the presence or in the absence of methanandamide (Met-AEA), a non-hydrolysable analogue of anandamide. The CB1R involvement was studied by using the specific inhibitor (SR141716) or mimicking its activation by adding a permeable cAMP analogue (8Br-cAMP). By an immunocytochemistry approach it was shown that the Met-AEA inhibits the bicarbonate-dependent translocation of CB1R from the post-equatorial to equatorial region of sperm head. In addition it was found that Met-AEA is able to prevent the bicarbonate-induced increase in membrane disorder and the cholesterol extraction, both preliminary to capacitation, acting through a CB1R-cAMP mediated pathway, as indicated by MC540 and filipin staining, EPR spectroscopy and biochemical analysis on whole membranes (CB1R activity) and on membrane enriched fraction (C/P content and anisotropy).

CONCLUSIONS/SIGNIFICANCE: Altogether, these data demonstrate that the endocannabinoid system strongly inhibits the process of sperm capacitation, acting as membrane stabilizing agent, thus increasing the basic knowledge on capacitation-related signaling and potentially opening new perspectives in diagnostics and therapeutics of male infertility.

摘要

背景

哺乳动物精子在雌性生殖道内获得其完全受精能力(所谓的获能),在那里它们逐渐暴露于抑制和刺激分子的逆浓度梯度中。

方法/主要发现:在本研究中,评估了内源性大麻素(anandamide)和碳酸氢盐对这个过程的影响,内源性大麻素是一种根据其浓度可以激活或抑制大麻素受体的内源性大麻素,而碳酸氢盐是一种卵道激活分子,以研究 1 型大麻素受体 (CB1R) 在对完成获能至关重要的脂质膜重塑过程中所发挥的作用。为此,在存在或不存在甲氧基去甲胺(Met-AEA)的情况下,体外培养公猪精子在碳酸氢盐刺激下进行获能条件下孵育,Met-AEA 是内源性大麻素的非水解类似物。通过使用特异性抑制剂(SR141716)或通过添加可渗透的 cAMP 类似物(8Br-cAMP)模拟其激活来研究 CB1R 的参与。通过免疫细胞化学方法表明,Met-AEA 抑制 CB1R 从精子头部赤道区到赤道区的碳酸氢盐依赖性易位。此外,还发现 Met-AEA 能够阻止碳酸氢盐诱导的膜无序增加和胆固醇提取,这两者都是获能的前提,通过 CB1R-cAMP 介导的途径起作用,如 MC540 和 filipin 染色、EPR 光谱和整个膜(CB1R 活性)和膜富集部分(C/P 含量和各向异性)的生化分析所示。

结论/意义:总之,这些数据表明内源性大麻素系统强烈抑制精子获能过程,作为膜稳定剂,从而增加对与获能相关的信号转导的基本认识,并为男性不育症的诊断和治疗开辟新的前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b64/3150387/a9f4d866c3ef/pone.0023038.g001.jpg

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