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首页> 外文期刊>Psychopharmacology >LSD but not lisuride disrupts prepulse inhibition in rats by activating the 5-HT2A receptor
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LSD but not lisuride disrupts prepulse inhibition in rats by activating the 5-HT2A receptor

机译:LSD而非5-丁烯二脲通过激活5-HT 2A 受体破坏大鼠的前搏抑制

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摘要

Rationale Compounds that activate the 5-HT2A receptor, such as lysergic acid diethylamide (LSD), act as hallucinogens in humans. One notable exception is the LSD congener lisuride, which does not have hallucinogenic effects in humans even though it is a potent 5-HT2A agonist. LSD and other hallucinogens have been shown to disrupt prepulse inhibition (PPI), an operational measure of sensorimotor gating, by activating 5-HT2A receptors in rats.
机译:原理激活5-HT 2A 受体的化合物,如麦角酰二乙胺(LSD),在人体中起致幻剂的作用。一个值得注意的例外是LSD同源物lisuride,尽管它是有效的5-HT 2A 激动剂,但对人体没有致幻作用。 LSD和其他致幻剂已被证明可以通过激活大鼠的5-HT 2A 受体来破坏前脉冲抑制(PPI),这是感觉运动门控的一种操作手段。

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