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氯氮平对乙醇动机特性的影响。

Clozapine's effects on ethanol's motivational properties.

作者信息

Thrasher M J, Freeman P A, Risinger F O

机构信息

Department of Behavioral Neuroscience, Portland Alcohol Research Center, Oregon Health Sciences University 97201-3098, USA.

出版信息

Alcohol Clin Exp Res. 1999 Aug;23(8):1377-85.

Abstract

BACKGROUND

Although dopamine D1 and D2 receptors have been implicated in ethanol's motivational effects, little is known about the contribution of dopamine D4 receptors. The present experiments examined the effects of clozapine, a dopamine D4 receptor antagonist, on ethanol's aversive, rewarding, stimulant, and reinforcing properties.

METHODS

For taste conditioning, adult male Swiss-Webster mice received five conditioning trials consisting of 1-hr access to 0.2 M NaCl. After NaCl access on trials 1-4, subjects received clozapine (0, 1, or 2 mg/kg) followed 30 min later by 0, 2, or 4 g/kg ethanol. For place conditioning, Swiss-Webster mice received six pairings of a tactile stimulus with ethanol (2 g/kg, intraperitoneally), clozapine (1 mg/kg, intraperitoneally) + ethanol, or clozapine alone. Locomotor activity in a 30-min test was determined in Swiss-Webster mice receiving 0, 0.5, or 1.0 mg/kg clozapine and 0, 1, or 2 g/kg ethanol. In a drinking study, separate groups of adult male C57BL/6J mice were allowed 30-min access to either 10% v/v ethanol mixed in 10% w/v sucrose or 10% sucrose without ethanol. During testing, both groups were given 0 or 1 mg/kg clozapine 30 min before fluid access.

RESULTS

Ethanol flavor pairings during taste conditioning reduced subsequent flavor intakes, indicating the development of conditioned taste aversion. Clozapine reduced the magnitude of 4 g/kg ethanol-conditioned aversion only on trial 4 at the 2 mg/kg dose. Conditioned place preference for the ethanol-paired stimulus was not altered by clozapine. Clozapine alone did not produce either conditioned preference or aversion. Ethanol-stimulated activity was reduced by clozapine treatment. However, clozapine alone did not alter locomotor activity levels. Clozapine reduced sucrose consumption but did not alter ethanol/sucrose intake.

CONCLUSIONS

These data suggest that clozapine influences a limited range of ethanol-motivated behaviors. Specifically, dopamine D4 receptors appear important for ethanol's stimulant effect and possibly ethanol aversion, but not ethanol reward and reinforcement.

摘要

背景

尽管多巴胺D1和D2受体与乙醇的动机效应有关,但关于多巴胺D4受体的作用知之甚少。本实验研究了多巴胺D4受体拮抗剂氯氮平对乙醇的厌恶、奖赏、兴奋和强化特性的影响。

方法

在味觉条件反射实验中,成年雄性瑞士-韦伯斯特小鼠接受五次条件反射试验,每次试验可接触0.2M NaCl 1小时。在第1-4次试验接触NaCl后,小鼠接受氯氮平(0、1或2mg/kg),30分钟后再接受0、2或4g/kg乙醇。在位置条件反射实验中,瑞士-韦伯斯特小鼠接受六次触觉刺激与乙醇(2g/kg,腹腔注射)、氯氮平(1mg/kg,腹腔注射)+乙醇或单独氯氮平的配对。在30分钟的测试中,测定接受0、0.5或1.0mg/kg氯氮平以及未接受或接受0、1或2g/kg乙醇的瑞士-韦伯斯特小鼠的运动活性。在一项饮水研究中,将成年雄性C57BL/6J小鼠分成不同组,分别给予30分钟时间接触10% v/v乙醇与10% w/v蔗糖混合液或不含乙醇的10%蔗糖溶液。在测试期间,两组小鼠在接触液体前30分钟均给予0或1mg/kg氯氮平。

结果

味觉条件反射期间的乙醇味道配对减少了随后的味道摄入量,表明形成了条件性味觉厌恶。氯氮平仅在第4次试验中以2mg/kg剂量降低了4g/kg乙醇引起的厌恶程度。氯氮平未改变对与乙醇配对刺激的条件性位置偏好。单独使用氯氮平既未产生条件性偏好也未产生厌恶。氯氮平治疗降低了乙醇刺激的活性。然而,单独使用氯氮平未改变运动活性水平。氯氮平减少了蔗糖消耗,但未改变乙醇/蔗糖摄入量。

结论

这些数据表明氯氮平影响有限范围的乙醇驱动行为。具体而言,多巴胺D4受体似乎对乙醇的兴奋作用以及可能的乙醇厌恶很重要,但对乙醇奖赏和强化不重要。

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