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内源性阿片肽:小鼠脑中其受体亲和力的比较评估

Endogenous opioid peptides: comparative evaluation of their receptor affinities in the mouse brain.

作者信息

Garzón J, Sánchez-Blázquez P, Höllt V, Lee N M, Loh H H

出版信息

Life Sci. 1983;33 Suppl 1:291-4. doi: 10.1016/0024-3205(83)90500-3.

Abstract

The affinities of certain endogenous opioid peptides and related sequences for mu, delta and k opiate receptors have been determined in membrane preparations from mouse brain. It was found that the KIs for the delta receptor changed very little when the sequence of the enkephalins was enlarged; on the contrary, the mu and especially the k activity were highly dependent not only on the specificity of the sequence but also on the length of the peptide. Most of the peptides have similar affinities for more than one receptor type. The enkephalins are the most selective for the delta receptor. beta-Endorphin, BAM-12P, BAM-22P, peptide E and dynorphin A display the best potency at the mu site. Dynorphin A (1-8), dynorphin A and dynorphin B are the most selective for the k site.

摘要

已在小鼠脑的膜制剂中测定了某些内源性阿片肽及其相关序列对μ、δ和κ阿片受体的亲和力。结果发现,当脑啡肽序列延长时,δ受体的抑制常数(KI)变化很小;相反,μ受体活性,尤其是κ受体活性不仅高度依赖于序列的特异性,还依赖于肽的长度。大多数肽对不止一种受体类型具有相似的亲和力。脑啡肽对δ受体的选择性最高。β-内啡肽、BAM-12P、BAM-22P、肽E和强啡肽A在μ受体位点表现出最佳效力。强啡肽A(1-8)、强啡肽A和强啡肽B对κ受体位点的选择性最高。

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