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致幻剂与血清素5-羟色胺受体介导的信号通路

Hallucinogens and Serotonin 5-HT Receptor-Mediated Signaling Pathways.

作者信息

López-Giménez Juan F, González-Maeso Javier

机构信息

Instituto de Biomedicina y Biotecnología de Cantabria IBBTEC-CSIC, 39011, Santander, Cantabria, Spain.

Department of Physiology and Biophysics, School of Medicine, Virginia Commonwealth University, Richmond, VA, 23298, USA.

出版信息

Curr Top Behav Neurosci. 2018;36:45-73. doi: 10.1007/7854_2017_478.

Abstract

The neuropsychological effects of naturally occurring psychoactive chemicals have been recognized for millennia. Hallucinogens, which include naturally occurring chemicals such as mescaline and psilocybin, as well as synthetic compounds, such as lysergic acid diethylamide (LSD), induce profound alterations of human consciousness, emotion, and cognition. The discovery of the hallucinogenic effects of LSD and the observations that LSD and the endogenous ligand serotonin share chemical and pharmacological profiles led to the suggestion that biogenic amines like serotonin were involved in the psychosis of mental disorders such as schizophrenia. Although they bind other G protein-coupled receptor (GPCR) subtypes, studies indicate that several effects of hallucinogens involve agonist activity at the serotonin 5-HT receptor. In this chapter, we review recent advances in understanding hallucinogen drug action through characterization of structure, neuroanatomical location, and function of the 5-HT receptor.

摘要

天然存在的精神活性化学物质的神经心理学效应已被认识了数千年。致幻剂包括天然存在的化学物质如三甲氧苯乙胺和裸盖菇素,以及合成化合物如麦角酸二乙酰胺(LSD),可引起人类意识、情感和认知的深刻改变。LSD致幻作用的发现以及LSD与内源性配体血清素具有相同化学和药理学特征的观察结果,提示血清素等生物胺与精神分裂症等精神障碍的精神病有关。尽管它们与其他G蛋白偶联受体(GPCR)亚型结合,但研究表明致幻剂的几种效应涉及血清素5-HT受体的激动剂活性。在本章中,我们通过对5-HT受体的结构、神经解剖位置和功能的表征,综述了在理解致幻剂药物作用方面的最新进展。

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