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戊巴比妥诱导的小鼠多动:阿片类机制作用可忽略不计

Pentobarbital-induced hyperactivity in mice: negligible role of opioid mechanisms.

作者信息

Vetulani J, Pavone F, Battaglia M, Sansone M

机构信息

Istituto di Psicobiologia e Psicofarmacologia, CNR, Roma, Italy.

出版信息

Pharmacol Biochem Behav. 1989 Aug;33(4):927-9. doi: 10.1016/0091-3057(89)90496-6.

Abstract

Subhypnotic doses (10 and 20 mg/kg) of pentobarbital significantly elevated locomotor activity measured for 30 min in CD-1 mice. The hyperactivity was also observed in mice recovering from pentobarbital-induced (50 mg/kg) sleep (measurements starting 15 min after recovery of righting reflex). Naloxone in doses up to 4 mg/kg did not affect significantly the pentobarbital-induced hyperactivity in any experiment; a dose of 8 mg/kg only partially attenuated the hyperactivity induced by a dose of 20 mg/kg of pentobarbital, but did not affect significantly either the stimulatory effect of a low subhypnotic dose (10 mg/kg) or the posthypnotic hyperactivity. This suggests a negligible involvement of opioid mechanisms in the hyperactivity induced by pentobarbital.

摘要

戊巴比妥的亚催眠剂量(10和20毫克/千克)显著提高了CD - 1小鼠30分钟内的运动活性。在从戊巴比妥诱导(50毫克/千克)睡眠中恢复的小鼠中也观察到了多动(在翻正反射恢复后15分钟开始测量)。在任何实验中,高达4毫克/千克剂量的纳洛酮对戊巴比妥诱导的多动均无显著影响;8毫克/千克的剂量仅部分减弱了20毫克/千克戊巴比妥诱导的多动,但对低亚催眠剂量(10毫克/千克)的刺激作用或催眠后多动均无显著影响。这表明阿片类机制在戊巴比妥诱导的多动中参与程度可忽略不计。

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