Department of Pharmaco-Biology, University of Calabria, Arcavacata di Rende, Cosenza, Italy.
Anat Rec (Hoboken). 2010 Feb;293(2):298-309. doi: 10.1002/ar.21042.
Recently, the endocannabinoid (EC) system and the presence of CB1 receptor (CB1-R), have been identified in human sperm. However, the effects of EC receptor ligands such as anandamide (N-arachidonoylethanolamine) and the role of EC system in male fertility is still largely unexplored. In the present study, we investigated the ultrastructural compartmentalization of CB1-R and analyzed the effects of its stimulation by using a stable analog of anandamide, 2-methylarachidonyl-2'-fluoro-ethylamide (MET-F-AEA). We focused particularly on sperm survival and acrosin activity. The study of human sperm anatomy by transmission electron microscopy with immunogold analysis revealed the location of the CB1-R prevalently in the sperm membranes of the head and interestingly on the mitochondria. The effect of different concentrations of MET-F-AEA from 100 nM to 1 microM evidenced a significant decrease of sperm survival. Interestingly, we analyzed this negative effect at molecular level, testing the EC action on different known sperm survival targets. MET-F-AEA-treatment decreased both pBCL2 and pAkt, two prosurvival proteins, and increased pPTEN expression which is the main regulator of the PI3K/Akt pathway. Moreover, a biphasic effect was observed with increasing MET-F-AEA concentrations on the acrosin activity. The blockage of the CB1-R by using its selective antagonist SR141716 (rimonabant) induced an opposite action on sperm survival supporting a role for this receptor in the biology of the male gamete.
最近,内源性大麻素(EC)系统和 CB1 受体(CB1-R)在人类精子中被发现。然而,EC 受体配体(如花生四烯酸乙醇胺)的作用以及 EC 系统在男性生育中的作用在很大程度上仍未得到探索。在本研究中,我们研究了 CB1-R 的超微结构区室化,并分析了使用花生四烯酸乙醇胺的稳定类似物 2-甲基花生四烯酰基-2'-氟乙基酰胺(MET-F-AEA)刺激其的作用。我们特别关注精子的存活率和顶体酶活性。通过透射电子显微镜和免疫金分析研究人类精子解剖结构,发现 CB1-R 主要位于头部的精子膜上,有趣的是,还位于线粒体上。不同浓度(从 100 nM 到 1 μM)的 MET-F-AEA 的作用表明精子存活率显著降低。有趣的是,我们在分子水平上分析了这种负面影响,测试了 EC 对不同已知的精子存活靶点的作用。MET-F-AEA 处理降低了两种促生存蛋白 pBCL2 和 pAkt 的表达,并增加了 PI3K/Akt 通路的主要调节剂 pPTEN 的表达。此外,随着 MET-F-AEA 浓度的增加,顶体酶活性呈双相变化。使用其选择性拮抗剂 SR141716(利莫那班)阻断 CB1-R 会对精子存活率产生相反的作用,支持该受体在男性配子生物学中的作用。