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某些多巴胺受体激动剂对家鸡(原鸡)和大鼠中硝西泮诱导睡眠的影响。

Influence of some dopaminoceptor agents on nitrazepam-induced sleep in the domestic fowl (Gallus domesticus) and rats.

作者信息

Wambebe C

出版信息

Jpn J Pharmacol. 1986 Mar;40(3):357-65. doi: 10.1254/jjp.40.357.

Abstract

The influence of apomorphine, levodopa and haloperidol was studied on nitrazepam sleep using young chicks and rats. In addition, the influence of dopamine and ADTN was studied in young chicks. Nitrazepam dose-dependently (0.4-51.2 mg/kg, i.p.) induced behavioural sleep in chicks. However, higher doses of nitrazepam (12.8-51.2 mg/kg, i.p.) were required to induce behavioural sleep in rats. Dopamine (12.5-100 mg/kg, i.p.) and ADTN (2.5-80 mg/kg, i.p.) delayed the onset but prolonged nitrazepam sleep in chicks: these effects were statistically significant. Levodopa (12.5-100 mg/kg, s.c.) and apomorphine (0.2-0.8 mg/kg, s.c.) profoundly delayed the onset and shortened the duration of nitrazepam sleep in both chicks and rats. Noradrenaline (20-80 mg/kg, i.p.) shortened the onset and prolonged nitrazepam sleep in chicks. Pimozide (1-8 mg/kg, i.p.) potentiated nitrazepam sleep and antagonized the effects of dopamine, levodopa and ADTN on nitrazepam sleep in chicks. Similarly, haloperidol (0.5-1.0 mg/kg, i.p.) potentiated nitrazepam sleep and antagonized the effects of levodopa and apomorphine on nitrazepam sleep in rats. The EEG synchronization and decreased EMG induced by nitrazepam (1.6 mg/kg, i.p., and 12.8 mg/kg, i.p., for chicks and rats, respectively) were antagonized by levodopa (12.5 mg/kg, s.c.). The behavioural and electroencephalographical results suggest that enhancement of dopaminergic neurotransmission may be involved in the mechanisms of wakefulness in both chicks and rats.

摘要

使用幼雏和大鼠研究了阿扑吗啡、左旋多巴和氟哌啶醇对硝西泮睡眠的影响。此外,还研究了多巴胺和ADTN对幼雏的影响。硝西泮(腹腔注射,剂量为0.4 - 51.2 mg/kg)在幼雏中剂量依赖性地诱导行为性睡眠。然而,在大鼠中诱导行为性睡眠需要更高剂量的硝西泮(腹腔注射,12.8 - 51.2 mg/kg)。多巴胺(腹腔注射,12.5 - 100 mg/kg)和ADTN(腹腔注射,2.5 - 80 mg/kg)延迟了幼雏中硝西泮睡眠的起始,但延长了其睡眠时间:这些效应具有统计学意义。左旋多巴(皮下注射,12.5 - 100 mg/kg)和阿扑吗啡(皮下注射,0.2 - 0.8 mg/kg)在幼雏和大鼠中均显著延迟了硝西泮睡眠的起始并缩短了其持续时间。去甲肾上腺素(腹腔注射,20 - 80 mg/kg)缩短了幼雏中硝西泮睡眠的起始并延长了其睡眠时间。匹莫齐特(腹腔注射,1 - 8 mg/kg)增强了幼雏中硝西泮睡眠,并拮抗了多巴胺、左旋多巴和ADTN对硝西泮睡眠的影响。同样,氟哌啶醇(腹腔注射,0.5 - 1.0 mg/kg)增强了大鼠中硝西泮睡眠,并拮抗了左旋多巴和阿扑吗啡对硝西泮睡眠的影响。左旋多巴(皮下注射,12.5 mg/kg)拮抗了硝西泮(分别以腹腔注射1.6 mg/kg和12.8 mg/kg给予幼雏和大鼠)诱导的脑电图同步化以及肌电图降低。行为学和脑电图结果表明,多巴胺能神经传递的增强可能参与了幼雏和大鼠的觉醒机制。

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