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γ-内啡肽和Nα-乙酰-γ-内啡肽通过阿片类和非阿片类机制干扰伏隔核中不同的多巴胺能系统。

gamma-Endorphin and N alpha-acetyl-gamma-endorphin interfere with distinct dopaminergic systems in the nucleus accumbens via opioid and non-opioid mechanisms.

作者信息

van Ree J M, Gaffori O, Kiraly I

出版信息

Life Sci. 1984 Apr 2;34(14):1317-24. doi: 10.1016/0024-3205(84)90002-x.

Abstract

Low doses (10 ng) of the dopamine agonist apomorphine induced hypolocomotion when injected into the nucleus accumbens of rats. This behavioral response was antagonized by local treatment with either the opioid peptide gamma-endorphin (gamma E) or the non-opioid peptide N alpha-acetyl-gamma-endorphin (Ac gamma E) in a dose of 100 pg. High doses of apomorphine (10 micrograms) r amphetamine (2 micrograms) injected into the nucleus accumbens resulted in hyperlocomotion. This response was blocked by pretreatment with gamma E but not with Ac gamma E. This effect of gamma E could be prevented by local treatment with naloxone. Neither peptides interfered with the apomorphine-induced stereotyped sniffing when the substances were injected into the nucleus caudatus. It is concluded that gamma E and Ac gamma E differentially interact with distinct dopaminergic systems in the nucleus accumbens of the rat brain via an opioid and a non-opioid mechanism, suggesting that the peptide fragments originating from pro-opiomelanocortin may be specifically implicated in the control of dopaminergic activity in this brain area.

摘要

低剂量(10纳克)的多巴胺激动剂阿扑吗啡注射到大鼠伏隔核中会诱发运动减少。这种行为反应可被局部注射100皮克的阿片肽γ-内啡肽(γE)或非阿片肽Nα-乙酰-γ-内啡肽(AcγE)所拮抗。高剂量的阿扑吗啡(10微克)或苯丙胺(2微克)注射到伏隔核中会导致运动增多。这种反应可被γE预处理阻断,但不能被AcγE阻断。γE的这种作用可被局部注射纳洛酮预防。当将这些物质注射到尾状核中时,两种肽均不干扰阿扑吗啡诱导的刻板嗅探。结论是,γE和AcγE通过阿片类和非阿片类机制与大鼠脑伏隔核中不同的多巴胺能系统发生不同的相互作用,这表明源自阿片-促黑素原皮质素的肽片段可能特别参与该脑区多巴胺能活性的控制。

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