Wisconsin National Primate Research Center, University of Wisconsin, Madison, WI 53715-1299, USA.
Adv Exp Med Biol. 2013;784:253-73. doi: 10.1007/978-1-4614-6199-9_12.
Since the discovery of the G-protein coupled receptor 54 (kisspeptin receptor) and its ligand, kisspeptin, our understanding of the neurobiological mechanisms that govern the pituitary-gonadal axis has evolved dramatically. In this chapter, we have reviewed progress regarding the relationship between kisspeptin and puberty, and have proposed a novel hypothesis for the role of kisspeptin signaling in the onset of this crucial developmental event. According to this hypothesis, although kisspeptin neurons in the arcuate nucleus (ARC) are critical for puberty, this is simply because these cells are an integral component of the hypothalamic GnRH pulse generating mechanism that drives intermittent release of the decapeptide, as an increase in GnRH is obligatory for the onset of puberty. In our model, ARC kisspeptin neurons play no "regulatory" role in controlling the timing of puberty. Rather, as a component of the neural network responsible for GnRH pulse generation, they subserve upstream regulatory mechanisms that are responsible for the timing of puberty.
自从发现 G 蛋白偶联受体 54(促性腺激素释放肽受体)及其配体促性腺激素释放肽以来,我们对调节垂体-性腺轴的神经生物学机制的理解发生了巨大的变化。在本章中,我们回顾了促性腺激素释放肽与青春期之间的关系,并提出了一个关于促性腺激素释放肽信号在这一关键发育事件发生中的作用的新假说。根据这一假说,尽管弓状核(ARC)中的促性腺激素释放肽神经元对青春期至关重要,但这仅仅是因为这些细胞是驱动十肽间歇性释放的下丘脑 GnRH 脉冲生成机制的一个组成部分,因为 GnRH 的增加是青春期开始的必要条件。在我们的模型中,ARC 促性腺激素释放肽神经元在控制青春期开始时间方面没有“调节”作用。相反,作为负责 GnRH 脉冲生成的神经网络的一部分,它们服务于负责青春期开始时间的上游调节机制。