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黑皮质素传递的阻断会抑制可卡因奖赏效应。

Blockade of melanocortin transmission inhibits cocaine reward.

作者信息

Hsu Richard, Taylor Jane R, Newton Samuel S, Alvaro John D, Haile Colin, Han G, Hruby Victor J, Nestler Eric J, Duman Ronald S

机构信息

Laboratory of Molecular Psychiatry, Center for Genes and Behaviour, Department of Psychiatry, Yale University School of Medicine, New Haven, CT 06508, USA.

出版信息

Eur J Neurosci. 2005 Apr;21(8):2233-42. doi: 10.1111/j.1460-9568.2005.04038.x.

Abstract

Melanocortins and the melanocortin-4 receptor (MC4-R) are enriched in the nucleus accumbens, a brain region that has been implicated in the rewarding action of cocaine and other drugs of abuse. In the present study we use a number of rat behavioral models to show that infusion of a melanocortin peptide antagonist into the nucleus accumbens blocks the reinforcing, incentive motivational, and locomotor sensitizing effects of cocaine. We also show that locomotor responses to repeated cocaine exposure are completely blocked in MC4-R null mutant mice and reduced in Agouti mice that overexpress an endogenous inhibitor of melanocortins in the brain. The results also demonstrate that cocaine administration increases the expression of MC4-R in the nucleus accumbens and striatum, and that MC4-R is co-localized with prodynorphin in medium spiny neurons in the nucleus accumbens. Together, these findings indicate that the behavioral actions of cocaine are dependent on activation of MC4-R, and suggest that upregulation of this receptor by drug exposure may contribute to sensitization of these behavioral responses. Modulation of cocaine reward is a novel action of the melanocortin-MC4-R system and could be targeted for the development of new medications for cocaine addiction.

摘要

促黑素细胞激素和促黑素细胞激素4受体(MC4-R)在伏隔核中含量丰富,伏隔核是一个与可卡因及其他滥用药物的奖赏作用有关的脑区。在本研究中,我们使用多种大鼠行为模型来表明,向伏隔核中注入促黑素细胞激素肽拮抗剂可阻断可卡因的强化、激励动机和运动致敏作用。我们还表明,在MC4-R基因敲除突变小鼠中,对重复暴露于可卡因的运动反应完全被阻断,而在大脑中过度表达内源性促黑素细胞激素抑制剂的刺豚鼠中,这种反应则有所减弱。结果还表明,给予可卡因会增加伏隔核和纹状体中MC4-R的表达,并且MC4-R与强啡肽原在伏隔核的中等多棘神经元中共定位。这些发现共同表明,可卡因的行为作用依赖于MC4-R的激活,并表明药物暴露导致该受体上调可能有助于这些行为反应的致敏。调节可卡因奖赏是促黑素细胞激素-MC4-R系统的一种新作用,可为开发治疗可卡因成瘾的新药提供靶点。

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