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钙调蛋白抑制剂三氟拉嗪可减弱大鼠吗啡诱导的条件性位置偏爱行为的形成与表达。

Calmodulin inhibitor trifluoperazine attenuates the development and expression of morphine-induced conditioned place preference in rats.

作者信息

Ye Xiang-Feng, Lu Ying, Zhang Pan, Liang Jian-Hui

机构信息

Department of Neuropharmacology, National Institute on Drug Dependence, Peking University, 38 Xueyuan Road, Haidian District, Beijing 100083, PR China.

出版信息

Eur J Pharmacol. 2004 Feb 23;486(3):265-71. doi: 10.1016/j.ejphar.2004.01.002.

Abstract

The effect of trifluoperazine, a calmodulin inhibitor, on morphine-induced conditioned place preference was examined in rats. Morphine (5, 10 mg/kg, i.p.) produced significant place preference for the drug-associated place. Trifluoperazine significantly suppressed the development as well as the expression of morphine-induced place preference in a dose-dependent manner, but it neither produced place preference or aversion, nor affected locomotor activity. Injection of 0.5 and 1.0 mg/kg apomorphine, a dopamine receptor agonist, did not alter the inhibition by trifluoperazine of morphine-induced place preference. Verapamil, at the dose that failed to change the place preference induced by morphine, enhanced the inhibition by trifluoperazine of morphine-induced place preference. These findings provide the first demonstration that trifluoperazine attenuates morphine-induced conditioned place preference in rats. The action of trifluoperazine might be produced through its inhibition of calmodulin, but is probably not related to dopamine receptor blockade.

摘要

在大鼠中研究了钙调蛋白抑制剂三氟拉嗪对吗啡诱导的条件性位置偏爱效应。吗啡(5、10毫克/千克,腹腔注射)产生了对药物相关位置的显著位置偏爱。三氟拉嗪以剂量依赖性方式显著抑制吗啡诱导的位置偏爱的形成及表达,但它既不产生位置偏爱也不产生厌恶,也不影响运动活性。注射多巴胺受体激动剂阿扑吗啡(0.5和1.0毫克/千克)并未改变三氟拉嗪对吗啡诱导的位置偏爱的抑制作用。维拉帕米在未能改变吗啡诱导的位置偏爱的剂量下,增强了三氟拉嗪对吗啡诱导的位置偏爱的抑制作用。这些发现首次证明三氟拉嗪可减弱大鼠中吗啡诱导的条件性位置偏爱。三氟拉嗪的作用可能是通过其对钙调蛋白的抑制产生的,但可能与多巴胺受体阻断无关。

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