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Kiss1神经元的昼夜节律调节:对排卵前促性腺激素释放激素/促黄体生成素激增时间的影响。

Circadian regulation of Kiss1 neurons: implications for timing the preovulatory gonadotropin-releasing hormone/luteinizing hormone surge.

作者信息

Robertson Jessica L, Clifton Donald K, de la Iglesia Horacio O, Steiner Robert A, Kauffman Alexander S

机构信息

Departments of Biology, University of Washington, Seattle, Washington 98195, USA.

出版信息

Endocrinology. 2009 Aug;150(8):3664-71. doi: 10.1210/en.2009-0247. Epub 2009 May 14.

Abstract

The preovulatory GnRH/LH surge depends on the presence of estradiol (E(2)) and is gated by a circadian oscillator in the suprachiasmatic nucleus (SCN) that causes the surge to occur within a specific temporal window. Although the mechanisms by which the clock times the LH surge are unclear, evidence suggests that the SCN is linked to GnRH neurons through a multisynaptic pathway that includes neurons in the anteroventral periventricular nucleus (AVPV). Recently, Kiss1 neurons in the AVPV have been implicated in the surge mechanism, suggesting that they may integrate circadian and E(2) signals to generate the LH surge. We tested whether Kiss1 neurons display circadian patterns of regulation in synchrony with the temporal pattern of LH secretion. Mice housed in 14 h light, 10 h dark were ovariectomized, given E(2) capsules (or nothing), and transferred into constant darkness. Two days later, the mice were killed at various times of day and their LH and Kiss1 levels assessed. In E(2)-treated females, LH levels were low except during late subjective day (indicative of an LH surge). Similarly, AVPV Kiss1 expression and c-fos coexpression in Kiss1 neurons showed circadian patterns that peaked coincident with LH. These temporal changes in Kiss1 neurons occurred under steady-state E(2) and constant environmental conditions, suggesting that Kiss1 neurons are regulated by circadian signals. In the absence of E(2), animals displayed no circadian pattern in LH secretion or Kiss1 expression. Collectively, these findings suggest that the LH surge is controlled by AVPV Kiss1 neurons whose activity is gated by SCN signals in an E(2)-dependent manner.

摘要

排卵前促性腺激素释放激素/促黄体生成素高峰依赖于雌二醇(E₂)的存在,并由视交叉上核(SCN)中的昼夜节律振荡器控制,该振荡器使高峰在特定的时间窗口内出现。尽管时钟调节促黄体生成素高峰的机制尚不清楚,但有证据表明,SCN通过包括室旁前腹核(AVPV)神经元在内的多突触途径与促性腺激素释放激素神经元相连。最近,AVPV中的Kiss1神经元与高峰机制有关,这表明它们可能整合昼夜节律和E₂信号以产生促黄体生成素高峰。我们测试了Kiss1神经元是否与促黄体生成素分泌的时间模式同步显示昼夜节律调节模式。将饲养在14小时光照、10小时黑暗环境中的小鼠进行卵巢切除,给予E₂胶囊(或不给予),然后转移到持续黑暗环境中。两天后,在一天中的不同时间处死小鼠,并评估它们的促黄体生成素和Kiss1水平。在接受E₂治疗的雌性小鼠中,促黄体生成素水平较低,除非在主观日后期(表明促黄体生成素高峰)。同样,AVPV中Kiss1的表达以及Kiss1神经元中c-fos的共表达显示出昼夜节律模式,其峰值与促黄体生成素一致。Kiss1神经元的这些时间变化发生在稳态E₂和恒定环境条件下,表明Kiss1神经元受昼夜节律信号调节。在没有E₂的情况下,动物的促黄体生成素分泌或Kiss1表达没有昼夜节律模式。总的来说,这些发现表明促黄体生成素高峰由AVPV Kiss1神经元控制,其活动以E₂依赖的方式由SCN信号控制。

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