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拮抗猫体内由麦角酸二乙酰胺(LSD)诱导的肢体轻弹行为的药物。

Drugs that antagonize limb flick behavior induced by D-lysergic acid diethylamide (LSD) in cats.

作者信息

Haigler H J, Spring D D

出版信息

Psychopharmacology (Berl). 1979 Jun 28;64(1):31-4. doi: 10.1007/BF00427341.

Abstract

In cats observed in their home cages limb flicks (LF) are a sensitive measure of the behavioral effects of LSD. LF induced by LSD (50 microgram/kg) were blocked by dextrorphan (0.6 mg/kg), dextromethorphan (0.6 mg/kg), and imipramine (5 mg/kg) at doses that did not produce ataxia or sleep. Levorphanol (0.6 mg/kg), a narcotic that is a congener of dextrorphan, did not block LF induced by LSD possibly because it produced an excitatory effect when given alone. Pentobarbital at low doses (2 and 4 mg/kg) increased the number of LF induced by LSD but at a high dose (8 mg/kg) decreased LF induced by LSD either by producing ataxia, so the cats tended to remain immobile, or by producing sleep. Chlorpromazine (CPZ) at three doses (2, 4, and 8 mg/kg) attenuated the effects of LSD on LF, but did not block LF as completely as the above three blocking drugs, and produced ataxia and sleep.

摘要

在关在笼中的猫身上观察到,肢体轻弹(LF)是衡量麦角酸二乙胺(LSD)行为效应的一个敏感指标。LSD(50微克/千克)诱发的LF可被右啡烷(0.6毫克/千克)、右美沙芬(0.6毫克/千克)和丙咪嗪(5毫克/千克)阻断,这些剂量不会产生共济失调或睡眠。左啡诺(0.6毫克/千克)是右啡烷的同类麻醉药,它不能阻断LSD诱发的LF,可能是因为它单独给药时会产生兴奋作用。低剂量(2和4毫克/千克)的戊巴比妥会增加LSD诱发的LF数量,但高剂量(8毫克/千克)时,戊巴比妥要么通过产生共济失调使猫倾向于保持不动,要么通过产生睡眠来减少LSD诱发的LF。三种剂量(2、4和8毫克/千克)的氯丙嗪(CPZ)会减弱LSD对LF的影响,但不像上述三种阻断药物那样能完全阻断LF,并且会产生共济失调和睡眠。

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