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α-氟哌噻吨增加大鼠慢波:多巴胺受体阻断的作用

alpha-Flupenthixol increases slow-wave in rats: effect of dopamine receptor blockade.

作者信息

Fornal C, Wojcik W J, Radulovacki M

出版信息

Neuropharmacology. 1982 Apr;21(4):323-5. doi: 10.1016/0028-3908(82)90095-8.

Abstract

alpha-Flupenthixol (0.2 mg/kg, i.p.), a dopamine receptor blocker, significantly increased slow-wave sleep and decreased wakefulness in rats when administered either at the onset of a 12-hr light period or a 12-hr dark period. The same dose of the drug strongly antagonized the dopamine-mediated stereotype produced by an injection of apomorphine (1 mg/kg, i.p.) for at least 9-hr, indicating that dopamine receptors were blocked throughout most of the recording session. The results suggest a relationship between the blockade of dopamine receptors and the increase of slow-wave sleep time.

摘要

α-氟哌噻吨(0.2毫克/千克,腹腔注射)是一种多巴胺受体阻滞剂,在12小时光照期或12小时黑暗期开始时给药,可显著增加大鼠的慢波睡眠并减少觉醒。相同剂量的该药物能强烈拮抗由注射阿扑吗啡(1毫克/千克,腹腔注射)产生的多巴胺介导的刻板行为,持续至少9小时,这表明在大部分记录过程中多巴胺受体都被阻断。结果提示多巴胺受体阻断与慢波睡眠时间增加之间存在关联。

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