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哺乳期大鼠弓状核 kisspeptin/神经激肽 B 神经元投射的特征及其调节。

Characterisation of arcuate nucleus kisspeptin/neurokinin B neuronal projections and regulation during lactation in the rat.

机构信息

Division of Neuroscience, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, Oregon 97006, USA.

出版信息

J Neuroendocrinol. 2011 Jan;23(1):52-64. doi: 10.1111/j.1365-2826.2010.02076.x.

Abstract

Lactation results in negative energy balance in the rat leading to decreased gonadotrophin-releasing hormone (GnRH) release and anoestrus. Inhibited GnRH release may be a result of decreased stimulatory tone from neuropeptides critical for GnRH neuronal activity, such as kisspeptin (Kiss1) and neurokinin B (NKB). The present study aimed to identify neuronal projections from the colocalised population of Kiss1/NKB cells in the arcuate nucleus (ARH) using double-label immunohistochemistry to determine where this population may directly regulate GnRH neuronal activity. Additionally, the present study further examined lactation-induced changes in the Kiss1 system that could play a role in decreased GnRH release. The colocalised ARH Kiss1/NKB fibres projected primarily to the internal zone of the median eminence (ME) where they were in close proximity to GnRH fibres; however, few Kiss1/NKB fibres from the ARH were seen at the level of GnRH neurones in the preoptic area (POA). Arcuate Kiss1/NKB peptide levels were decreased during lactation consistent with previous mRNA data. Surprisingly, anteroventral periventricular (AVPV) Kiss1 peptide levels were increased, whereas Kiss1 mRNA levels were decreased during lactation, suggesting active inhibition of peptide release. These findings indicate ARH Kiss1/NKB and AVPV Kiss1 appear to be inhibited during lactation, which may contribute to decreased GnRH release and subsequent reproductive dysfunction. Furthermore, the absence of a strong ARH Kiss1/NKB projection to the POA suggests regulation of GnRH by this population occurs primarily at the ME level via local projections.

摘要

哺乳期大鼠会出现负能平衡,导致促性腺激素释放激素(GnRH)释放减少和乏情。GnRH 释放受抑制可能是关键的 GnRH 神经元活动神经肽刺激减少的结果,如 kisspeptin(Kiss1)和神经激肽 B(NKB)。本研究旨在使用双重免疫组织化学鉴定弓状核(ARH)中 Kiss1/NKB 细胞的共定位群体的神经元投射,以确定该群体如何直接调节 GnRH 神经元活动。此外,本研究还进一步研究了哺乳期 Kiss1 系统的变化,这些变化可能在 GnRH 释放减少中起作用。共定位的 ARH Kiss1/NKB 纤维主要投射到正中隆起的内区(ME),在那里它们与 GnRH 纤维非常接近;然而,在视前区(POA)的 GnRH 神经元水平上,很少看到 ARH 的 Kiss1/NKB 纤维。哺乳期 ARH Kiss1/NKB 肽水平下降,与先前的 mRNA 数据一致。令人惊讶的是,前脑室下 Periventricular(AVPV) Kiss1 肽水平升高,而 Kiss1 mRNA 水平在哺乳期下降,表明肽释放受到积极抑制。这些发现表明,ARH Kiss1/NKB 和 AVPV Kiss1 在哺乳期似乎受到抑制,这可能导致 GnRH 释放减少和随后的生殖功能障碍。此外,ARH Kiss1/NKB 对 POA 的投射不强表明,该群体对 GnRH 的调节主要发生在 ME 水平,通过局部投射。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/780f/3118985/ab2c41641a55/nihms297343f1.jpg

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