Basolateral amygdala CB1 receptors gate HPA axis activation and context-cocaine memory strength during reconsolidation

被引:11
|
作者
Higginbotham, Jessica A. [1 ]
Jones, Nicole M. [1 ]
Wang, Rong [1 ]
Christian, Robert J. [1 ]
Ritchie, Jobe L. [1 ]
McLaughlin, Ryan J. [1 ,2 ,3 ]
Fuchs, Rita A. [1 ,2 ,3 ]
机构
[1] Washington State Univ, Coll Vet Med, Dept Integrat Physiol & Neurosci, Pullman, WA 99164 USA
[2] Washington State Univ, Alcohol & Drug Abuse Res Program, Pullman, WA 99164 USA
[3] Washington State Univ, Translat Addict Res Collaborat, Pullman, WA 99164 USA
关键词
CORTICOTROPIN-RELEASING HORMONE; EMOTIONAL AROUSAL; ENDOCANNABINOID SYSTEM; CANNABINOID RECEPTORS; DORSAL HIPPOCAMPUS; PREFRONTAL CORTEX; SEEKING; STRESS; CORTICOSTERONE; INVOLVEMENT;
D O I
10.1038/s41386-020-00919-x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Re-exposure to a cocaine-associated context triggers craving and relapse through the retrieval of salient context-drug memories. Upon retrieval, context-drug memories become labile and temporarily sensitive to modification before they are reconsolidated into long-term memory stores. The effects of systemic cannabinoid type 1 receptor (CB1R) antagonism indicate that CB1R signaling is necessary for cocaine-memory reconsolidation and associated glutamatergic plasticity in the basolateral amygdala (BLA); however, the contribution of BLA CB1R signaling to cocaine-memory reconsolidation is unknown. Here, we assessed whether intra-BLA CB1R manipulations immediately after cocaine-memory retrieval alter cocaine-memory strength indexed by subsequent drug context-induced cocaine-seeking behavior in an instrumental rodent model of drug relapse. Administration of the CB1R antagonist, AM251 (0.3 mu g/hemisphere) into the BLA increased subsequent drug context-induced cocaine-seeking behavior in a memory retrieval-dependent and anatomically selective manner. Conversely, the CB1R agonist, WIN55,212-2 (0.5 or 5 mu g/hemisphere) failed to alter this behavior. In follow-up experiments, cocaine-memory retrieval elicited robust hypothalamic-pituitary-adrenal axis activation, as indicated by a rise in serum corticosterone concentrations. Intra-BLA AM251 administration during memory reconsolidation selectively increased this cocaine-memory retrieval-induced corticosterone response. Intra-BLA corticosterone administration (3 or 10 ng/hemisphere) during memory reconsolidation did not augment subsequent cocaine-seeking behavior, suggesting that CB1R-dependent effects of corticosterone on memory strength, if any, are mediated outside of the BLA. Together, these findings suggest that CB1R signaling in the BLA gates cocaine-memory strength, possibly by diminishing the impact of cue-induced arousal on the integrity of the reconsolidating memory trace or on the efficacy of the memory reconsolidation process.
引用
收藏
页码:1554 / 1564
页数:11
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