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亲吻素:一种多功能肽系统,在生殖、癌症和心血管系统中发挥作用。

Kisspeptins: a multifunctional peptide system with a role in reproduction, cancer and the cardiovascular system.

作者信息

Votsi E, Roussos D, Katsikis I, Karkanaki A, Kita M, Panidis D

机构信息

Division of Endocrinology and Human Reproduction, 2nd Department of Obstetrics and Gynecology, Aristotle University of Thessaloniki, Greece.

出版信息

Hippokratia. 2008;12(4):205-10.

Abstract

The pairing of the kisspeptins (KP) with the KISS1 (GPR54) receptor has received growing attention since the description of the receptor as a molecular switch for puberty. The role of KP and its receptor, GPR54, in puberty is the most exciting finding made in the field of reproductive biology since the discovery of Gonadotropin Releasing Hormone (GnRH) in 1970s. A significant body of evidence across several species now suggests that KISS1 (GPR54) activation is a critical point in the commencement of puberty, although further investigation is required to characterize the interaction between KP and GnRH cascade. Given such pivotal roles of kisspeptins and GPR54 as gatekeepers of reproductive function, and the proven ability of sex steroids to physiologically regulate this system, it is plausible that environmental compounds with ability to interfere oestrogen and/or androgen signaling (agonists or antagonists) may target the hypothalamic kiss-1/GPR54 system, thereby inducing functional alterations of the hypothalamic-pituitary-gonadal axis. Synthetic agonists targeting KISS1 (GPR54) may represent novel therapeutic agents for the treatment of hypogonadotrophic hypogonadism in some affected individuals. The diverse multifunctional nature of the KP is beginning to unravel. The unexpected role of these peptides in puberty has raised a number of important questions that remain to be answered.

摘要

自将KISS1(GPR54)受体描述为青春期的分子开关以来, kisspeptins(KP)与该受体的配对受到了越来越多的关注。自20世纪70年代发现促性腺激素释放激素(GnRH)以来, KP及其受体GPR54在青春期中的作用是生殖生物学领域最令人兴奋的发现。现在,多个物种的大量证据表明,KISS1(GPR54)的激活是青春期开始的关键点,尽管还需要进一步研究来描述KP与GnRH级联之间的相互作用。鉴于kisspeptins和GPR54作为生殖功能守门人的关键作用,以及性类固醇在生理上调节该系统的已证实能力,具有干扰雌激素和/或雄激素信号传导能力(激动剂或拮抗剂)的环境化合物可能靶向下丘脑Kiss-1/GPR54系统,从而诱导下丘脑-垂体-性腺轴的功能改变。靶向KISS1(GPR54)的合成激动剂可能代表了治疗某些受影响个体的性腺功能减退性性腺功能减退的新型治疗药物。KP多样的多功能性质正开始被揭示。这些肽在青春期中出人意料的作用引发了许多有待回答的重要问题。

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本文引用的文献

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