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阿片类药物与生殖。

Opioids and reproduction.

机构信息

Department of Gynecological Endocrinology and Reproductive Medicine, Medical University of Innsbruck, Innsbruck, Austria.

Department of Gynecological Endocrinology and Reproductive Medicine, Medical University of Innsbruck, Innsbruck, Austria.

出版信息

Vitam Horm. 2019;111:247-279. doi: 10.1016/bs.vh.2019.07.001. Epub 2019 Jul 26.

Abstract

More than 40years ago, the endogenous opioids were first described. Their role as important neuromodulators of pain and their influence on a variety of neuroendocrine control systems within the central nervous system has been recognized. More recently, endogenous opioids and their receptor have been identified in a variety of reproductive and non-reproductive tissues outside the central nervous system. What role the opioid system plays in these peripheral tissues and organs is not completely understood and thus the subjects of current research. In the central nervous system, endogenous opioids inhibit pulsatile Gonadotropin Releasing Hormone (GnRH) release, affecting the release of gonadotropins from the pituitary, and thus mediating stress response within the central nervous-pituitary-gonadal axes in both women and men-Peripherally, endogenous opioids have been demonstrated to be present-among other organs-in the pancreas and in the ovary, where they are produced by granulosa cells and may influence oocyte maturation. In men, endogenous opioids play a role in sperm production within the testis. Opioid antagonists such as naltrexone have been used to restore cyclicity in women through improvement in insulin resistance, GnRH-pulsatility and hyperandrogenemia stemming from specific pathophysiological conditions such as hypothalamic amenorrhea, polycystic ovarian syndrome, hyperinsulinemia, ovarian hyperstimulation syndrome. Opioid antagonists have also been used to treat male sexual disorders and male infertility. In summary, endogenous opioids exert a variety of actions within the reproductive system which are reviewed in this chapter.

摘要

40 多年前,首次描述了内源性阿片类物质。它们作为疼痛的重要神经调质的作用及其对中枢神经系统内各种神经内分泌控制系统的影响已得到认可。最近,在外周神经系统之外的各种生殖和非生殖组织中也鉴定出了内源性阿片类物质及其受体。阿片类系统在这些外周组织和器官中发挥什么作用尚不完全清楚,因此成为当前研究的主题。在内分泌系统中,内源性阿片类物质抑制促性腺激素释放激素(GnRH)的脉冲式释放,影响垂体促性腺激素的释放,从而调节女性和男性中枢神经系统-垂体-性腺轴中的应激反应。在外周,内源性阿片类物质已被证明存在于胰腺和卵巢等器官中,在这些器官中,它们由颗粒细胞产生,并可能影响卵母细胞的成熟。在男性中,内源性阿片类物质在睾丸中参与精子的产生。阿片类拮抗剂,如纳曲酮,已被用于通过改善特定病理生理条件(如下丘脑闭经、多囊卵巢综合征、高胰岛素血症、卵巢过度刺激综合征)引起的胰岛素抵抗、GnRH 脉冲性和高雄激素血症,来恢复女性的周期性。阿片类拮抗剂也被用于治疗男性性功能障碍和男性不育。总之,内源性阿片类物质在生殖系统中发挥着多种作用,本章对此进行了综述。

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