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Interactions between kisspeptin and neurokinin B in the control of GnRH secretion in the female rat

机译:Kisspeptin与神经激肽B之间的相互作用对雌性大鼠GnRH分泌的控制

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摘要

Neurokinin B (NKB) and its cognate receptor neurokinin 3 (NK3R) play a critical role in reproduction. NKB and NK3R are coexpressed with dynorphin (Dyn) and kisspeptin (Kiss1) genes in neurons of the arcuate nucleus (Arc). However, the mechanisms of action of NKB as a cotransmitter with kisspeptin and dynorphin remain poorly understood. We explored the role of NKB in the control of LH secretion in the female rat as follows. 1) We examined the effect of an NKB agonist (senktide, 600 pmol, administered into the lateral cerebral ventricle) on luteinizing hormone (LH) secretion. In the presence of physiological levels of estradiol (E2), senktide induced a profound increase in serum levels of LH and a 10-fold increase in the number of Kiss1 neurons expressing c-fos in the Arc (P < 0.01 for both). 2) We mapped the distribution of NKB and NK3R mRNAs in the central forebrain and found that both are widely expressed, with intense expression in several hypothalamic nuclei that control reproduction, including the Arc. 3) We studied the effect of E2 on the expression of NKB and NK3R mRNAs in the Arc and found that E2 inhibits the expression of both genes (P < 0.01) and that the expression of NKB and NK3R reaches its nadir on the afternoon of proestrus (when circulating levels of E2 are high). These observations suggest that NKB/NK3R signaling in Kiss1/NKB/Dyn-producing neurons in the Arc has a pivotal role in the control of gonadotropin-releasing hormone (GnRH)/LH secretion and its regulation by E2-dependent negative feedback in the rat.
机译:神经激肽B(NKB)及其同源受体神经激肽3(NK3R)在繁殖中起关键作用。 NKB和NK3R与强啡肽(Dyn)和Kisspeptin(Kiss1)基因在弓状核(Arc)的神经元中共表达。然而,关于NKB与kisepteptin和强啡肽的共递质的作用机理仍然知之甚少。我们探索了NKB在控制雌性大鼠LH分泌中的作用,如下所述。 1)我们检查了NKB激动剂(senktide,600 pmol,施用于大脑侧脑室)对促黄体激素(LH)分泌的影响。在生理水平的雌二醇(E2)存在下,senktide诱导血清中LH的水平显着增加,并且在Arc中表达c-fos的Kiss1神经元数量增加10倍(两者均P <0.01)。 2)我们绘制了NKB和NK3R mRNA在中央前脑中的分布图,发现二者均广泛表达,并在控制下丘脑的几个下丘脑核中强烈表达,包括Arc。 3)我们研究了E2对Arc中NKB和NK3R mRNA表达的影响,发现E2抑制了这两个基因的表达(P <0.01),而 NKB NK3R 在发情期下午(E2的循环水平很高时)达到最低点。这些观察结果表明弧中Kiss1 / NKB / Dyn产生神经元中的NKB / NK3R信号传导在控制促性腺激素释放激素(GnRH)/ LH分泌及其通过E2依赖性负反馈对大鼠的调节中起关键作用。

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