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5-(邻氯苯基)-1-甲基-7-硝基-1,3-二氢-2H-1,4-苯并二氮杂卓-2-酮(ID-390)与硝西泮相比对猫睡眠-觉醒周期的影响(作者译)

[Effects of 5-(o-chlorophenyl)-1-methyl-7-nitro-1, 3-dihydro-2HO1, 4-benzodiazepin-2-one (ID-390) as compared to nitrazepam on the sleep-wakefulness cycle in cats (author's transl)].

作者信息

Tsuchiya T, Fukushima H

出版信息

Nihon Yakurigaku Zasshi. 1977 May;73(4):437-47. doi: 10.1254/fpj.73.437.

Abstract

ID-690 was given at doses over 0.3 mg/kg, and increase in state of arousal and decrease in state of slow wave sleep were observed. Nitrazepam at doses over 1.0 mg/kg revealed similar effects. These agents increased incidences of paradoxical sleep at a low dose of 0.03 mg/kg. When ID-690 was given at doses over 0.3 mg/kg, the number and duration of incidences of paradoxical sleep decreased. Nitrazepam at doses over 0.1 mg/kg had a similar depressive effect on paradoxical sleep. These results suggest that these benzodiazepines have, dose-dependently, both facilitative and depressive actions on paradoxical sleep, and that the dose of these agents which affects arousal is not always the same as that which affects paradoxical sleep.

摘要

ID - 690以超过0.3毫克/千克的剂量给药时,观察到觉醒状态增加和慢波睡眠状态减少。硝西泮以超过1.0毫克/千克的剂量给药时显示出类似的效果。这些药物在0.03毫克/千克的低剂量时增加了异相睡眠的发生率。当ID - 690以超过0.3毫克/千克的剂量给药时,异相睡眠的发作次数和持续时间减少。硝西泮以超过0.1毫克/千克的剂量给药时对异相睡眠有类似的抑制作用。这些结果表明,这些苯二氮䓬类药物对异相睡眠具有剂量依赖性的促进和抑制作用,并且这些药物影响觉醒的剂量并不总是与影响异相睡眠的剂量相同。

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