Sigma-1受体
西格玛受体
受体
致幻剂
药理学
兴奋剂
内生
化学
阿片受体
变构调节剂
生物
生物化学
作者
Dominique Fontanilla,Molly Johannessen,Abdol R. Hajipour,Nicholas V. Cozzi,Meyer B. Jackson,Arnold E. Ruoho
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2009-02-13
卷期号:323 (5916): 934-937
被引量:455
标识
DOI:10.1126/science.1166127
摘要
The sigma-1 receptor is widely distributed in the central nervous system and periphery. Originally mischaracterized as an opioid receptor, the sigma-1 receptor binds a vast number of synthetic compounds but does not bind opioid peptides; it is currently considered an orphan receptor. The sigma-1 receptor pharmacophore includes an alkylamine core, also found in the endogenous compound N,N -dimethyltryptamine (DMT). DMT acts as a hallucinogen, but its receptor target has been unclear. DMT bound to sigma-1 receptors and inhibited voltage-gated sodium ion (Na + ) channels in both native cardiac myocytes and heterologous cells that express sigma-1 receptors. DMT induced hypermobility in wild-type mice but not in sigma-1 receptor knockout mice. These biochemical, physiological, and behavioral experiments indicate that DMT is an endogenous agonist for the sigma-1 receptor.
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