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在自行给药的大鼠戒断可卡因期间,其体内杏仁核促肾上腺皮质激素释放因子(CRF)的释放会增加。

In vivo CRF release in rat amygdala is increased during cocaine withdrawal in self-administering rats.

作者信息

Richter R M, Weiss F

机构信息

Department of Neuropharmacology, Scripps Research Institute, La Jolla, California 92037, USA.

出版信息

Synapse. 1999 Jun 15;32(4):254-61. doi: 10.1002/(SICI)1098-2396(19990615)32:4<254::AID-SYN2>3.0.CO;2-H.

Abstract

Previous studies have suggested a role for corticotropin-releasing factor (CRF) in the central nucleus of the amygdala (CeA) in the aversive and anxiogenic effects of withdrawal from opiates and ethanol. To test whether this role of CRF extends to cocaine withdrawal as well, the release of CRF in rat amygdala was monitored by intracranial microdialysis during a 12-hour session of intravenous cocaine self-administration and subsequent 12-hour cocaine withdrawal period. Cocaine self-administration tended to lower dialysate CRF concentrations to approximately 75% of CRF levels in controls. In contrast, subsequent cocaine withdrawal produced a profound increase in CRF release, which reached peak levels of approximately 400% of baseline between 11 and 12 hours post-cocaine. These results provide evidence that cocaine withdrawal activates CRF neurons in the amygdala, a site that has been implicated in emotional and anxiogenic effects of stress and drug withdrawal syndromes.

摘要

先前的研究表明,促肾上腺皮质激素释放因子(CRF)在杏仁核中央核(CeA)中对阿片类药物和乙醇戒断的厌恶及焦虑作用发挥着一定作用。为了检验CRF的这一作用是否也适用于可卡因戒断,在大鼠静脉注射可卡因自我给药12小时及随后12小时的可卡因戒断期内,通过颅内微透析监测大鼠杏仁核中CRF的释放。可卡因自我给药倾向于使透析液中CRF浓度降至对照组CRF水平的约75%。相比之下,随后的可卡因戒断导致CRF释放显著增加,在可卡因注射后11至12小时之间达到基线水平约400%的峰值。这些结果证明,可卡因戒断会激活杏仁核中的CRF神经元,该部位与应激的情绪及焦虑作用和药物戒断综合征有关。

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