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大鼠促黄体生成素分泌调节中的阿片-肾上腺素能-类固醇联系

Opioid-adrenergic-steroid connection in regulation of luteinizing hormone secretion in the rat.

作者信息

Kalra S P, Kalra P S

出版信息

Neuroendocrinology. 1984 May;38(5):418-26. doi: 10.1159/000123928.

Abstract

In this article we have attempted first to summarize the current information on the effects of each of the three neuronal systems - gonadal steroid concentrating neurons, catecholamine and opioid producing neurons - on various aspects of luteinizing hormone releasing hormone (LHRH) secretion. The salient features of the new information are: (1) gonadal steroids are capable of raising LHRH levels in the median eminence nerve terminals without changing LH (LHRH) secretion; (2) a chain of temporally related neural events in the preoptic-tuberal pathway precede the preovulatory LH release; (3) catecholamines may provide a permissive environment for appropriate function of LHRH neurons, and (4) the inhibitory influence of endogenous opioid peptides on LH release may be mediated by adrenergic neurons in the preoptic-tuberal pathway. Based on this information we have constructed a conceptual model which attempts to integrate the inputs of these three systems during the episodic basal and cyclic release of LH in the rat.

摘要

在本文中,我们首先尝试总结关于三种神经元系统——性腺类固醇浓缩神经元、儿茶酚胺和产生阿片样物质的神经元——对促黄体生成激素释放激素(LHRH)分泌各方面影响的当前信息。新信息的显著特点是:(1)性腺类固醇能够在正中隆起神经末梢提高LHRH水平,而不改变促黄体生成素(LH)(LHRH)分泌;(2)视前 - 结节通路中一系列时间相关的神经事件先于排卵前LH释放;(3)儿茶酚胺可能为LHRH神经元的正常功能提供一个允许的环境,以及(4)内源性阿片样肽对LH释放的抑制作用可能由视前 - 结节通路中的肾上腺素能神经元介导。基于这些信息,我们构建了一个概念模型,该模型试图整合大鼠LH在间歇性基础和周期性释放过程中这三种系统的输入。

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