多巴胺转运体
多巴胺
再摄取
伏隔核
有条件地点偏好
自噬
药理学
兴奋剂
多巴胺能
刺激
多巴胺质膜转运蛋白
多巴胺摄取抑制剂
化学
血清素
运输机
神经科学
生物
生物化学
受体
细胞凋亡
基因
作者
Maged M. Harraz,Prasun Guha,In Guk Kang,Evan R. Semenza,Adarsha P. Malla,Young Jun Song,Luke Reilly,Isaac Treisman,Pedro Cortés,Mark A. Coggiano,Vijayabhaskar Veeravalli,Rana Rais,Gianluigi Tanda,Solomon H. Snyder
标识
DOI:10.1038/s41380-020-00978-y
摘要
Cocaine exerts its stimulant effect by inhibiting dopamine reuptake leading to increased dopamine signaling. This action is thought to reflect binding of cocaine to the dopamine transporter (DAT) to inhibit its function. However, cocaine is a relatively weak inhibitor of DAT, and many DAT inhibitors do not share the behavioral actions of cocaine. We previously showed that toxic levels of cocaine induce autophagic neuronal cell death. Here, we show that subnanomolar concentrations of cocaine elicit neural autophagy in vitro and in vivo. Autophagy inhibitors reduce the locomotor stimulant effect of cocaine in mice. Cocaine-induced autophagy degrades transporters for dopamine but not serotonin in the nucleus accumbens. Autophagy inhibition impairs cocaine conditioned place preference in mice. Our findings indicate that autophagic degradation of DAT modulates behavioral actions of cocaine.
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