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β-内啡肽对小鼠脑桥/延髓中G蛋白的激活是由μ受体和假定的ε受体的刺激介导的。

Activation of G-proteins in the mouse pons/medulla by beta-endorphin is mediated by the stimulation of mu- and putative epsilon-receptors.

作者信息

Mizoguchi H, Narita M, Nagase H, Tseng L F

机构信息

Department of Anesthesiology, Medical College of Wisconsin, Milwaukee 53226, USA.

出版信息

Life Sci. 2000 Oct 20;67(22):2733-43. doi: 10.1016/s0024-3205(00)00852-3.

Abstract

The activation of mu-, delta- and kappa1-opioid receptors by their respective agonists increases the binding of the non-hydrolyzable GTP analog guanosine-5'-(gamma-thio)-triphosphate (GTPgammaS) to G proteins. Beta-endorphin is an endogenous opioid peptide which binds nonselectively to mu-, delta- and putative epsilon-opioid receptors. The present experiment was designed to determine which opioid receptors are involved in the stimulation of [35S]GTPgammaS binding induced by beta-endorphin in the mouse pons/medulla. The mouse pons/medulla membranes were incubated in an assay buffer containing 50 pM [35S]GTPgammaS, 30 microM GDP and various concentrations of beta-endorphin. Beta-endorphin (0.1 nM-10 microM) increased [35S]GTPgammaS binding in a concentration-dependent manner, and 10 microM beta-endorphin produced a maximal stimulation of approximately 260% over baseline. This stimulation of [35S]GTPgammaS binding by beta-endorphin was partially attenuated by the mu-opioid receptor antagonist beta-funaltrexamine (beta-FNA), but not by the delta-opioid receptor antagonist naltrindole (NTI) or the kappa1-opioid receptor antagonist nor-binaltorphimine (nor-BNI). Beta-endorphin stimulated [35S]GTPgammaS binding by about 80% in the presence of 10 microM beta-FNA, 30 nM NTI and 100 nM nor-BNI. The same concentrations of these antagonists completely blocked the stimulation of [35S]GTPgammaS binding induced by 10 microM [D-Ala2,NHPhe4,Gly-ol]enkephalin, [D-Pen(2,5)]enkephalin and U50,488H, respectively. Moreover, the residual stimulation of [35S]GTPgammaS binding induced by beta-endorphin in the presence of the three opioid receptor antagonists was significantly attenuated by 100 nM of the putative epsilon-opioid receptor partial agonist beta-endorphin (1-27). These results indicate that the stimulation of [35S]GTPgammaS binding induced by beta-endorphin is mediated by the stimulation of both mu- and putative epsilon-opioid receptors in the mouse pons/medulla.

摘要

μ-、δ-和κ1-阿片受体被各自的激动剂激活后,会增加不可水解的GTP类似物鸟苷-5'-(γ-硫代)-三磷酸(GTPγS)与G蛋白的结合。β-内啡肽是一种内源性阿片肽,它能非选择性地与μ-、δ-和假定的ε-阿片受体结合。本实验旨在确定在小鼠脑桥/延髓中,β-内啡肽诱导的[35S]GTPγS结合的刺激涉及哪些阿片受体。将小鼠脑桥/延髓膜在含有50 pM [35S]GTPγS、30 μM GDP和不同浓度β-内啡肽的测定缓冲液中孵育。β-内啡肽(0.1 nM - 10 μM)以浓度依赖的方式增加[35S]GTPγS结合,10 μM β-内啡肽产生的最大刺激比基线增加约260%。β-内啡肽对[35S]GTPγS结合的这种刺激被μ-阿片受体拮抗剂β-芬太尼(β-FNA)部分减弱,但未被δ-阿片受体拮抗剂纳曲吲哚(NTI)或κ1-阿片受体拮抗剂去甲二氢吗啡酮(nor-BNI)减弱。在存在10 μM β-FNA、30 nM NTI和100 nM nor-BNI的情况下,β-内啡肽刺激[35S]GTPγS结合约80%。相同浓度的这些拮抗剂分别完全阻断了10 μM [D-Ala2,NHPhe4,Gly-ol]脑啡肽、[D-Pen(2,5)]脑啡肽和U50,488H诱导的[35S]GTPγS结合的刺激。此外,在三种阿片受体拮抗剂存在的情况下,β-内啡肽诱导的[35S]GTPγS结合的残余刺激被100 nM假定的ε-阿片受体部分激动剂β-内啡肽(1 - 27)显著减弱。这些结果表明,β-内啡肽诱导的[35S]GTPγS结合的刺激是由小鼠脑桥/延髓中μ-和假定的ε-阿片受体的刺激介导的。

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