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纹状体特定细胞类型中DeltaFosB的过表达增强了对可卡因的动机。

Striatal cell type-specific overexpression of DeltaFosB enhances incentive for cocaine.

作者信息

Colby Christina R, Whisler Kim, Steffen Cathy, Nestler Eric J, Self David W

机构信息

Division of Molecular Psychiatry, Yale University School of Medicine and Connecticut Mental Health Center, New Haven, Connecticut 06508, USA.

出版信息

J Neurosci. 2003 Mar 15;23(6):2488-93. doi: 10.1523/JNEUROSCI.23-06-02488.2003.

Abstract

The transcription factor DeltaFosB accumulates in substance P-dynorphin-containing striatal neurons with repeated cocaine use. Here, we show that inducible transgenic DeltaFosB overexpression in this same striatal cell type facilitates acquisition of cocaine self-administration at low-threshold doses, consistent with increased sensitivity to the pharmacological effects of the drug. Importantly, DeltaFosB also enhances the degree of effort mice will exert to maintain self-administration of higher doses on a progressive ratio schedule of reinforcement, whereas levels of cocaine intake are not altered on less demanding fixed-ratio schedules. Acquisition and extinction of behavior reinforced by food pellets is not altered in DeltaFosB-overexpressing mice, indicating that DeltaFosB does not alter the capacity to learn an instrumental response or cause response perseveration in the absence of reinforcement. These data suggest that accumulation of DeltaFosB contributes to drug addiction by increasing the incentive properties of cocaine, an effect that could increase the risk for relapse long after cocaine use ceases.

摘要

随着反复使用可卡因,转录因子DeltaFosB在含有P物质-强啡肽的纹状体神经元中积累。在此,我们表明,在同一纹状体细胞类型中诱导性转基因过表达DeltaFosB有助于在低阈值剂量下习得可卡因自我给药行为,这与对该药物药理作用的敏感性增加相一致。重要的是,DeltaFosB还增强了小鼠在渐进性比率强化程序中为维持更高剂量自我给药所付出的努力程度,而在要求较低的固定比率程序中,可卡因摄入量并未改变。在过表达DeltaFosB的小鼠中,由食物颗粒强化的行为的习得和消退并未改变,这表明DeltaFosB不会改变学习工具性反应的能力,也不会在没有强化的情况下导致反应持续。这些数据表明,DeltaFosB的积累通过增加可卡因的激励特性而导致药物成瘾,这种效应可能在可卡因使用停止很久之后增加复发风险。

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