Discriminative Inhibitory Control of Cocaine Seeking Involves the Prelimbic Prefrontal Cortex

被引:51
作者
Mihindou, Claudia
Guillem, Karine
Navailles, Sylvia
Vouillac, Caroline
Ahmed, Serge H. [1 ]
机构
[1] Univ Bordeaux Segalen, Inst Malad Neurodegenerat, CNRS, UMR 5293, F-33076 Bordeaux, France
关键词
Behavioral inhibition; cognitive control; craving; prefrontal cortex; relapse; self-regulation; BASOLATERAL AMYGDALA; INDUCED REINSTATEMENT; CONDITIONED INHIBITION; VOLUNTARY SUPPRESSION; COGNITIVE REGULATION; RESPONSE-INHIBITION; RELAPSE PREVENTION; INFRALIMBIC CORTEX; EMOTION REGULATION; TASK-PERFORMANCE;
D O I
10.1016/j.biopsych.2012.08.011
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Recent neuroimaging studies have shown that people with cocaine addiction retain some degree of control over drug craving that correlates with neural activity in the lateral prefrontal cortex (PFC). Here, we report similar findings in a rat model of inhibitory control of cocaine seeking. Methods: Rats actively responding for cocaine were trained to stop responding when presented with a discriminative stimulus that signaled lack of reinforcement. Rats were then tested for inhibitory control of cocaine seeking in novel behavioral contexts and in circumstances when cocaine seeking is particularly intense (e.g., following drug priming). The role of neuronal activity in different subregions of the PFC was assessed using local pharmacologic inactivation and c-Fos immunohistochemistry. Results: Rats progressively acquired the ability to stop cocaine seeking, even during drug intoxication and after a long history of cocaine self-administration. Inhibitory control of cocaine seeking was flexible, sufficiently strong to block cocaine-primed reinstatement, and selectively depended on increased neuronal activity within the prelimbic PFC, which is considered the rodent functional homolog of the human lateral PFC. Conclusions: Parallel evidence in both animal models and humans indicate that recruitment of prefrontal inhibitory control of drug seeking is still functional after prolonged cocaine use. Preclinical investigation of the mechanisms underlying this capacity may contribute to designing new behavioral and/or pharmacologic strategies to promote its use for the prevention of relapse in addiction.
引用
收藏
页码:271 / 279
页数:9
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