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[镇痛药在神经元水平作用的可能机制假说]

[A hypothesis of the possible mechanism of the action of analgesic agents at the neuronal level].

作者信息

Artem'ev I Iu, Darinskiĭ Iu A, Sologub M I

出版信息

Eksp Klin Farmakol. 1992 Jan-Feb;55(1):16-8.

PMID:1363942
Abstract

The opiate analgetic promedol and non-opiate analgetics analgin, clonidine, baclofen, tolibut, vasopressin and calcitonin given in adequate doses block the inward electrosensitive sodium transmembrane ionic current of neurons. Like some drugs which do not exhibit any analgetic effect, promedol, analgin, clonidine, vasopressin and calcitonin also block the electrosensitive delayed potassium current. It is assumed that the blocking of the sodium ionic current may be one of the potential analgetic mechanisms at the neuronal level.

摘要

阿片类镇痛药普罗美多以及非阿片类镇痛药安乃近、可乐定、巴氯芬、托利布、血管加压素和降钙素在给予适当剂量时,可阻断神经元的内向电敏感钠跨膜离子电流。与一些不具有任何镇痛作用的药物一样,普罗美多、安乃近、可乐定、血管加压素和降钙素也能阻断电敏感延迟钾电流。据推测,钠电流的阻断可能是神经元水平潜在的镇痛机制之一。

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