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CB1基因敲除小鼠对奖励的敏感性降低。

Reduced sensitivity to reward in CB1 knockout mice.

作者信息

Sanchis-Segura Carles, Cline Brandon H, Marsicano Giovanni, Lutz Beat, Spanagel Rainer

机构信息

Department of Psychopharmacology, Central Institute for Mental Health, CIMH, University of Heidelberg, 68159 Mannheim, Germany.

出版信息

Psychopharmacology (Berl). 2004 Nov;176(2):223-32. doi: 10.1007/s00213-004-1877-8. Epub 2004 Apr 9.

DOI:10.1007/s00213-004-1877-8
PMID:15083252
Abstract

RATIONALE

Previous studies have demonstrated that the activation and blockade of the cannabinoid type 1 receptor (CB1) leads to an enhancement and decrease of the consumption of food and other orally ingested reinforcers, respectively.

OBJECTIVE

To gain further knowledge about the role of CB1 in sucrose/saccharin reinforcing efficacy and intake, we tested CB1 knockout (CB1-KO) and littermate wild-type (WT) control mice in several self-administration experimental protocols.

METHODS

Operant (fixed or progressive ratio schedule) and non-operant conditioning procedures were used. In addition, a choice analysis based on the "matching law" as well as a microstructural analysis of the intra-session pattern of self-administration was performed.

RESULTS

CB1-KO mice consume less sucrose under operant conditions or when using a two-bottle free choice procedure. Moreover, as revealed by additional behavioural analysis, CB1-KO mice exhibit a decreased sensitivity to the rewarding properties of sucrose. In agreement with this finding, the differences between WT and CB1-KO mice faded away when the palatability of sucrose was devaluated by adding quinine, but not when a non-caloric sweetener, saccharin, was available.

CONCLUSIONS

These results demonstrate a modulatory role of CB1 in the determination of the rewarding properties of sucrose and probably, as suggested by previous studies, other reinforcers.

摘要

原理

先前的研究表明,1型大麻素受体(CB1)的激活和阻断分别导致食物及其他经口摄入的强化物的消耗量增加和减少。

目的

为了进一步了解CB1在蔗糖/糖精强化效力和摄入量中的作用,我们在几种自我给药实验方案中对CB1基因敲除(CB1-KO)小鼠和同窝野生型(WT)对照小鼠进行了测试。

方法

采用操作性(固定或累进比率程序)和非操作性条件反射程序。此外,基于“匹配法则”进行了选择分析,并对自我给药的会话内模式进行了微观结构分析。

结果

在操作性条件下或使用双瓶自由选择程序时,CB1-KO小鼠消耗的蔗糖较少。此外,额外的行为分析表明,CB1-KO小鼠对蔗糖奖励特性的敏感性降低。与此发现一致的是,当通过添加奎宁降低蔗糖的适口性时,WT小鼠和CB1-KO小鼠之间的差异消失,但当提供无热量甜味剂糖精时,差异并未消失。

结论

这些结果证明了CB1在确定蔗糖奖励特性方面具有调节作用,并且可能如先前研究所暗示的,对其他强化物也有调节作用。

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