Lewis Sheena E, Maccarrone Mauro
School of Medicine, Centre for Public Health, Queen's University Belfast, Institute of Clinical Science, Grosvenor Road, Belfast BT12 6BJ, UK.
Pharmacol Res. 2009 Aug;60(2):126-31. doi: 10.1016/j.phrs.2009.02.009. Epub 2009 Mar 4.
In this review, we shall summarize the current knowledge on the endocannabinoid system (ECS), and on its involvement in the multifaceted process of male reproduction. In particular, we shall discuss the role of ECS in sperm biology and Sertoli cell proliferation and death, showing how endocannabinoids may regulate spermatogenesis and reproductive potential.
The available evidence highlights the existence of a distinctive network, including endocannabinoids and sex hormones, that warrants a successful pregnancy in mammals. In particular, it appears that the endocannabinoid-degrading enzyme FAAH (fatty acid amide hydrolase) has a central role in this array of signals, because it controls several steps of sperm biology, from motility to capacitation and acrosome reaction. Since the regulation of FAAH activity and expression by autocrine and paracrine factors may occur through genomic or non-genomic mechanisms mediated by type-1 cannabinoid receptor (CB1R) signaling, we also raise concerns about the use of CB1R agonists (like marijuana) or antagonists (like the anti-obesity drug Acomplia in subjects of reproductive age.
Based on the present data, we point out that FAAH might be a novel and potentially important target for the development of next generation therapeutics against infertility. In particular, a reduced reproductive potential seems to be paralleled by defective FAAH, suggesting that therapeutics able to enhance, rather than inhibit, enzyme activity might be useful fertility enhancers.
在本综述中,我们将总结关于内源性大麻素系统(ECS)及其在男性生殖多方面过程中所起作用的现有知识。特别是,我们将讨论ECS在精子生物学以及支持细胞增殖和死亡中的作用,展示内源性大麻素如何调节精子发生和生殖潜能。
现有证据突出了一个独特网络的存在,该网络包括内源性大麻素和性激素,对哺乳动物成功受孕至关重要。特别是,内源性大麻素降解酶FAAH(脂肪酸酰胺水解酶)似乎在这一系列信号中起着核心作用,因为它控制着精子生物学的几个步骤,从运动能力到获能和顶体反应。由于自分泌和旁分泌因子对FAAH活性和表达的调节可能通过由1型大麻素受体(CB1R)信号介导的基因组或非基因组机制发生,我们也对在育龄期受试者中使用CB1R激动剂(如大麻)或拮抗剂(如抗肥胖药物Acomplia)表示担忧。
基于目前的数据,我们指出FAAH可能是开发下一代抗不育疗法的一个新的且潜在重要的靶点。特别是,生殖潜能降低似乎与FAAH缺陷并行,这表明能够增强而非抑制酶活性的疗法可能是有用的生育增强剂。