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首页> 外文期刊>Molecular and Cellular Endocrinology >Neurobiological mechanisms underlying kisspeptin activation of gonadotropin-releasing hormone (GnRH) neurons at puberty.
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Neurobiological mechanisms underlying kisspeptin activation of gonadotropin-releasing hormone (GnRH) neurons at puberty.

机译:青春期促性腺激素释放激素(GnRH)神经元亲吻肽激活的神经生物学机制。

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摘要

Studies undertaken in many species indicate that kisspeptin-Gpr54 signaling is essential for the activation of gonadotropin-releasing hormone (GnRH) neurons to bring about puberty. Investigations in transgenic mouse models, in particular, have highlighted the importance of kisspeptin signaling at the level of the GnRH neuron itself in this process. This review aims to highlight current understanding of the neurobiological mechanisms underlying the kisspeptin activation of postnatal GnRH neurons. The three key features of the kisspeptin-Gpr54-GnRH neuron axis leading up to puberty are (i) the expression of adult-like levels of Gpr54 mRNA in GnRH neurons well in advance of puberty, (ii) a modest increase in the electrical response of GnRH neurons to Gpr54 activation across postnatal development and (iii), the "sudden" appearance of kisspeptin fibers surrounding GnRH neuron cell bodies/proximal dendrites just prior to puberty onset. These kisspeptin fibers are likely to originate from the kisspeptin population located in the rostral periventricular region of the third ventricle (RP3V). Together, available data suggest that the key step in the kisspeptin control of puberty lies in the control of kisspeptin synthesis within RP3V kisspeptin neurons that innervate GnRH neurons. This has recently been shown to be dependent upon circulating estradiol concentrations. As such, we propose that RP3V kisspeptin neurons represent a critical estradiol-dependent amplification mechanism brought into play relatively late in pubertal development to activate GnRH neurons and complete the process of puberty onset. Subsequently, in the adult female, this same circuitry is used to activate GnRH neurons to generate the cyclical preovulatory GnRH/LH surge.
机译:在许多物种中进行的研究表明,kisepteptin-Gpr54信号传导对于促性腺激素释放激素(GnRH)神经元的激活带来青春期至关重要。特别是在转基因小鼠模型中的研究突出了在此过程中在GnRH神经元自身水平上亲吻肽信号传导的重要性。这篇综述旨在突出当前对产后GnRH神经元亲吻肽激活的神经生物学机制的了解。 Kisspeptin-Gpr54-GnRH神经元轴导致青春期的三个关键特征是:(i)青春期之前GnRH神经元中成人样Gpr54 mRNA的表达水平;(ii)电反应适度增加GnRH神经元在整个出生后发育过程中对Gpr54活化的影响;(iii)刚好在青春期发作之前,围绕GnRH神经元细胞体/近端树突的吻肽纤维的“突然”出现。这些kisepteptin纤维很可能源自位于第三脑室(RP3V)的脑室周围区域的kisseptin种群。总之,现有数据表明,青春期Kisspeptin控制的关键步骤在于神经支配GnRH神经元的RP3V Kisspeptin神经元内Kisspeptin合成的控制。最近显示这取决于循环雌二醇浓度。因此,我们建议RP3V Kisspeptin神经元代表一个关键的雌二醇依赖性扩增机制,该机制在青春期发育的较晚才发挥作用,以激活GnRH神经元并完成青春期发作的过程。随后,在成年女性中,使用相同的电路激活GnRH神经元,以产生周期性排卵前GnRH / LH激增。

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