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滥用药物和压力会引发多巴胺神经元中一种常见的突触适应性变化。

Drugs of abuse and stress trigger a common synaptic adaptation in dopamine neurons.

作者信息

Saal Daniel, Dong Yan, Bonci Antonello, Malenka Robert C

机构信息

Nancy Pritzker Laboratory, Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Palo Alto, CA 94304, USA.

出版信息

Neuron. 2003 Feb 20;37(4):577-82. doi: 10.1016/s0896-6273(03)00021-7.

Abstract

Drug seeking and drug self-administration in both animals and humans can be triggered by drugs of abuse themselves or by stressful events. Here, we demonstrate that in vivo administration of drugs of abuse with different molecular mechanisms of action as well as acute stress both increase strength at excitatory synapses on midbrain dopamine neurons. Psychoactive drugs with minimal abuse potential do not cause this change. The synaptic effects of stress, but not of cocaine, are blocked by the glucocorticoid receptor antagonist RU486. These results suggest that plasticity at excitatory synapses on dopamine neurons may be a key neural adaptation contributing to addiction and its interactions with stress and thus may be an attractive therapeutic target for reducing the risk of addiction.

摘要

在动物和人类中,觅药行为和药物自我给药可由滥用药物本身或应激事件引发。在此,我们证明,给予具有不同作用分子机制的滥用药物以及急性应激,均可增强中脑多巴胺能神经元兴奋性突触的强度。滥用可能性极小的精神活性药物不会引起这种变化。应激而非可卡因的突触效应可被糖皮质激素受体拮抗剂RU486阻断。这些结果表明,多巴胺能神经元兴奋性突触的可塑性可能是导致成瘾及其与应激相互作用的关键神经适应性变化,因此可能是降低成瘾风险的一个有吸引力的治疗靶点。

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