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毒蕈碱型胆碱能参与吗啡和可乐定对小鼠镇痛作用的比较。

A comparison of muscarinic cholinergic involvement in the antinociceptive effects of morphine and clonidine in the mouse.

作者信息

Lipman J J, Spencer P S

出版信息

Eur J Pharmacol. 1980 Jun 27;64(4):249-58. doi: 10.1016/0014-2999(80)90232-0.

Abstract

The antinociceptive effects (AE) of morphine and clonidine were examined in the mouse tail immersion test (48 degrees C). The interactions of these two agents with cholinergic (muscarinic) and anticholinergic (antimuscarinic) drugs were examined with respect to antinociceptive effect. Physostigmine, administered peripherally and intracerebroventricularly (i.c.v.) increased the AE of both morphine and clonidine. Atropine sulphate (but not atropine methylnitrate) antagonized the AE of both morphine and clonidine in a dose-dependent manner. Oxotremorine (OTMN) produced an AE that was additive with that of morphine and clonidine without being synergistic. These findings are discussed in terms of possible cholinergic mechanisms involved in the AEs produced by morpine and clonidine.

摘要

在小鼠尾部浸入试验(48摄氏度)中检测了吗啡和可乐定的抗伤害感受作用(AE)。就抗伤害感受作用而言,研究了这两种药物与胆碱能(毒蕈碱型)和抗胆碱能(抗毒蕈碱型)药物的相互作用。外周和脑室内(i.c.v.)给予毒扁豆碱可增强吗啡和可乐定的AE。硫酸阿托品(而非硝酸甲基阿托品)以剂量依赖方式拮抗吗啡和可乐定的AE。氧化震颤素(OTMN)产生的AE与吗啡和可乐定的AE相加,但无协同作用。根据吗啡和可乐定产生的AE中可能涉及的胆碱能机制对这些发现进行了讨论。

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