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低剂量阿扑吗啡诱导大鼠睡眠。

Sleep induced by low doses of apomorphine in rats.

作者信息

Mereu G P, Scarnati E, Paglietti E, Quarantotti B P, Chessa P, Di Chiara G, Gessa G L

出版信息

Electroencephalogr Clin Neurophysiol. 1979 Feb;46(2):214-9. doi: 10.1016/0013-4694(79)90071-3.

Abstract

The effect of apomorphine on the EEG of freely moving rats was studied. Apomorphine at the dose of 1 mg/kg caused stereotypy and a marked reduction of total sleep. On the contrary, acute subcutaneous administration of apomorphine at the dose of 100 microgram/kg, or less, markedly increased the amount of total sleep (corresponding mostly to synchronized sleep). Moreover, the infusion of apomorphine (80 microgram/kg/h) for 4 h doubled the duration of slow and REM sleep. The hypnotic effect of apomorphine was prevented by neuroleptics, such as pimozide, benzperidol and L-sulpiride, at doses which, per se, did not modify the EEG of the animals. These results suggest the existence in the CNS of DA receptors mediating sleep.

摘要

研究了阿扑吗啡对自由活动大鼠脑电图的影响。1毫克/千克剂量的阿扑吗啡会引起刻板行为并使总睡眠时间显著减少。相反,急性皮下注射100微克/千克或更低剂量的阿扑吗啡会显著增加总睡眠时间(主要对应同步睡眠)。此外,以80微克/千克/小时的剂量输注阿扑吗啡4小时,可使慢波睡眠和快速眼动睡眠的持续时间加倍。抗精神病药物如匹莫齐特、苯哌利多和L-舒必利可在不改变动物脑电图的剂量下阻止阿扑吗啡的催眠作用。这些结果表明中枢神经系统中存在介导睡眠的多巴胺受体。

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