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[内啡肽对阿片受体的比较活性]

[Comparative activity of endorphins on the opiate receptors].

作者信息

Vallée E, Chambon J P, Delahayes J

出版信息

C R Acad Hebd Seances Acad Sci D. 1977 Jul 18;285(3):257-60.

PMID:198160
Abstract

Displacement of naloxone from membranes of Rat brain by alpha, beta and gamma-endorphins with and without Na+ in the incubating medium has been studied. beta-endorphin shows a higher affinity for the opiate receptors and a stronger agonist property than morphine. alpha and gamma-endorphins have a much lower affinity than morphine and a marked antagonist characteristic. This study suggests the possibility of naturally occurring antagonists of the opiate receptors.

摘要

研究了在有无钠离子存在的孵育介质中,α、β和γ-内啡肽对大鼠脑细胞膜上纳洛酮的置换作用。β-内啡肽对阿片受体的亲和力高于吗啡,激动特性也强于吗啡。α和γ-内啡肽的亲和力远低于吗啡,且具有明显的拮抗特性。该研究提示了阿片受体天然拮抗剂存在的可能性。

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