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三甲氧苯乙胺:对听觉惊吓的兴奋作用被5-羟色胺2拮抗剂阻断。

Mescaline: excitatory effects on acoustic startle are blocked by serotonin2 antagonists.

作者信息

Davis M

机构信息

Department of Psychiatry, Yale University, New Haven, CT 06508.

出版信息

Psychopharmacology (Berl). 1987;93(3):286-91. doi: 10.1007/BF00187244.

Abstract

The ability of serotonin2 (5-HT2) antagonists to block the excitatory effects of mescaline on the acoustic startle reflex were analyzed. Mescaline (20 mg/kg) caused a consistent increase in the amplitude of the acoustic startle reflex. This effect was blocked in a dose-related fashion by the 5-HT2 antagonist ritanserin (ED50 dose = 0.25 mg/kg IP). In contrast, even a high dose of ritanserin (2.0 mg/kg) did not block the excitatory effects of amphetamine on startle. Other 5-HT2 antagonists (ketanserin, cinanserin, LY 53857) also blocked mescaline's effect, whereas the 5-HT1 antagonist pindolol (5 mg/kg) did not. These results support the hypothesis that the behavioral effects of hallucinogens are mediated by agonist actions at 5-HT2 receptors.

摘要

分析了5-羟色胺2(5-HT2)拮抗剂阻断三甲氧苯乙胺对听觉惊吓反射兴奋作用的能力。三甲氧苯乙胺(20毫克/千克)可使听觉惊吓反射的幅度持续增加。5-HT2拮抗剂利坦色林以剂量相关方式阻断了这一效应(半数有效剂量=0.25毫克/千克腹腔注射)。相比之下,即使是高剂量的利坦色林(2.0毫克/千克)也不能阻断苯丙胺对惊吓反射的兴奋作用。其他5-HT2拮抗剂(酮色林、西那色林、LY 53857)也能阻断三甲氧苯乙胺的作用,而5-HT1拮抗剂吲哚洛尔(5毫克/千克)则不能。这些结果支持这样一种假说,即致幻剂的行为效应是由5-HT2受体的激动剂作用介导的。

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