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γ型内啡肽对大鼠α-促黑素细胞激素释放的影响。

The effect of gamma-type endorphins on alpha-MSH release in the rat.

作者信息

de Rotte A A, van Wimersma Greidanus T B, van de Buuse M, Andringa-Bakker E A, de Wied D

出版信息

Life Sci. 1985 Jul 22;37(3):263-71. doi: 10.1016/0024-3205(85)90652-6.

Abstract

Neuroleptic drugs increase the level of alpha-melanotropin (alpha-MSH) in the blood of the rat. We have investigated whether neuroleptic-like peptides, the gamma-type endorphins, also affect alpha-MSH release. A structure-activity study revealed that (des-enkephalin)-gamma-endorphin (DE gamma E, beta-LPH-(66-77), beta-endorphin-(6-17)) is able to increase plasma alpha-MSH levels after intracerebroventricular injection, while the longer gamma-type endorphins, i.e. gamma E (beta-LPH-(61-77)), beta-endorphin-(1-17)), and DT gamma E (beta-LPH-(62-77), beta-endorphin-(2-17)) were without effect in the dosage used. A dose-response study revealed a more or less bell-shaped relationship for the effect of DE gamma E on plasma alpha-MSH levels. The effect of DE gamma E could not be counteracted by apomorphine or naloxone. The observations indicate that DE gamma E increases plasma alpha-MSH levels in a way distinct from that of haloperidol and the opiate peptide beta-endorphin. On the other hand, a time-course of plasma alpha-MSH levels after DE gamma E administration resembled the one which has been seen after haloperidol injection. From experiments performed on pituitary neurointermediate lobes incubated in vitro, it seems not likely that DE gamma E acts directly on the dopamine receptors of the pituitary in affecting alpha-MSH release. In conclusion, it appears that DE gamma E affects alpha-MSH levels in plasma in a way distinct from that of the neuroleptic drug haloperidol and of the opiate-peptide beta-endorphin.

摘要

抗精神病药物会提高大鼠血液中α-促黑素(α-MSH)的水平。我们研究了类抗精神病肽——γ型内啡肽是否也会影响α-MSH的释放。一项构效关系研究表明,(去甲脑啡肽)-γ-内啡肽(DEγE,β-促脂解素-(66 - 77),β-内啡肽-(6 - 17))在脑室内注射后能够提高血浆α-MSH水平,而较长的γ型内啡肽,即γE(β-促脂解素-(61 - 77))、β-内啡肽-(1 - 17))以及DTγE(β-促脂解素-(62 - 77),β-内啡肽-(2 - 17))在所使用的剂量下没有效果。一项剂量反应研究表明,DEγE对血浆α-MSH水平的影响呈现出或多或少的钟形关系。DEγE的作用不能被阿扑吗啡或纳洛酮抵消。这些观察结果表明,DEγE以一种不同于氟哌啶醇和阿片肽β-内啡肽的方式提高血浆α-MSH水平。另一方面,DEγE给药后血浆α-MSH水平的时间进程类似于氟哌啶醇注射后所观察到的情况。从对体外培养的垂体神经中间叶进行的实验来看,DEγE似乎不太可能通过直接作用于垂体的多巴胺受体来影响α-MSH的释放。总之,DEγE似乎以一种不同于抗精神病药物氟哌啶醇和阿片肽β-内啡肽的方式影响血浆中的α-MSH水平。

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