阿片肽在髓质背侧心脏调节机制中的选择性翻译后加工

W. Millington, M. D. Hirsch
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引用次数: 1

摘要

摘要:吗啡和其他阿片类药物的降压特性已经被记录了一个多世纪,但直到最近二十年,我们才开始了解这些有害作用的神经元机制。这些发现的历史已经广为传播;立体选择性阿片受体在20世纪70年代初首次被发现,随后不久,通过分离其内源性配体,阿片肽-内啡肽,氨基啡肽和亮氨酸啡肽,以及啡肽。这三个阿片肽家族均由孤束核(NTS)和其他脑心脏调节部位的神经元表达,为阿片药物的心血管副作用提供了解剖学基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Selective Post-Translational Processing of Opioid Peptides in Cardioregulatory Mechanisms of the Dorsal Medulla
Abstract : The hypotensive properties of morphine and other opiate drugs have been well documented for over a century, yet only in the past two decades have we begun to understand the neuronal mechanisms responsible for these ofttimes deleterious effects. The history of these discoveries has been widely disseminated; stereoselective opioid receptors were first identified in the early 1970s followed soon thereafter by isolation of their endogeneous ligands, the opioid peptides beta-endorphin, met-and leu-en-kephalin, and dynorphin. All three opioid peptide families are expressed by neurons in the nucleus tractus solitrarius (NTS) and other cardioregulatory brain sites, providing an anatomical basis for the cardiovascular side effects of opiate drugs.
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