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垂体细胞上存在阿片受体的证据。

Evidence for opiate receptors on pituicytes.

作者信息

Lightman S L, Ninkovic M, Hunt S P, Iversen L L

出版信息

Nature. 1983;305(5931):235-7. doi: 10.1038/305235a0.

Abstract

A hypothalamo-neurohypophyseal enkephalinergic pathway has been described and the pars nervosa of the rat pituitary contains enkephalin-like material which may coexist in vasopressin and oxytocin terminals. At the level of the pars nervosa itself, stereospecific opiate receptors with properties very similar to those of brain receptors have been described, and opiates have been shown to inhibit the release of both vasopressin and oxytocin. The location of the opiate receptors involved has been presumed to be pre-terminal on the neurosecretory fibres. Using an autoradiographic technique to visualize opiate receptors, however, we now report that destruction of the neurosecretory fibres following pituitary stalk section does not result in a significant change in the neural lobe opiate receptor population. This suggests that the opiate receptors within the neural lobe may be present on pituicytes rather than on neurosecretory fibres.

摘要

一条下丘脑 - 神经垂体脑啡肽能通路已被描述,大鼠垂体神经部含有脑啡肽样物质,其可能与血管加压素和催产素终末共存。在神经部本身的水平,已描述了具有与脑受体非常相似特性的立体特异性阿片受体,并且已证明阿片类物质可抑制血管加压素和催产素的释放。所涉及的阿片受体的位置被推测在神经分泌纤维的终末前。然而,使用放射自显影技术来可视化阿片受体,我们现在报告垂体柄切断后神经分泌纤维的破坏不会导致神经叶阿片受体数量的显著变化。这表明神经叶内的阿片受体可能存在于垂体细胞上而非神经分泌纤维上。

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