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抗阿片肽血清对大鼠地西泮诱导摄食的拮抗作用。

Antagonism of diazepam-induced feeding in rats by antisera to opioid peptides.

作者信息

González Y, Fernández-Tomé M P, Sánchez-Franco F, del Río J

出版信息

Life Sci. 1984 Sep 24;35(13):1423-9. doi: 10.1016/0024-3205(84)90401-6.

Abstract

Diazepam-induced feeding in rats is antagonized not only by the opiate antagonist naloxone but also intraventricular administration of specific antisera to the endogenous opioid peptides met-enkephalin or beta-endorphin. Pituitary beta-endorphin is probably not implicated in the diazepam effect since blockade with the glucocorticoid dexamethasone of the release of beta-endorphin from the anterior pituitary does not modify the diazepam-induced feeding, which is however prevented by TRH, a suggested physiological antagonist of some of the effects of opioid peptides. The possible central participation of both beta-endorphin and met-enkephalin in the ingestive behavior induced by diazepam gives further support to the postulated physiological role of endogenous opioids in appetite regulation.

摘要

地西泮诱导的大鼠进食不仅受到阿片拮抗剂纳洛酮的拮抗,还受到脑室内注射针对内源性阿片肽甲硫氨酸脑啡肽或β-内啡肽的特异性抗血清的拮抗。垂体β-内啡肽可能与地西泮的作用无关,因为用糖皮质激素地塞米松阻断β-内啡肽从前垂体的释放并不会改变地西泮诱导的进食,然而促甲状腺激素(TRH)可阻止这种进食,TRH是阿片肽某些作用的一种推测的生理拮抗剂。β-内啡肽和甲硫氨酸脑啡肽可能在中枢参与地西泮诱导的摄食行为,这进一步支持了内源性阿片类物质在食欲调节中假定的生理作用。

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