氮氧化能系统参与苯二氮卓类药物对小鼠的催眠作用。

Polish journal of pharmacology Pub Date : 2004-11-01
Sylwia Talarek, Sylwia Fidecka
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引用次数: 0

摘要

研究了一氧化氮(NO)对地西泮、氯二氮环氧化物和氯硝西泮的小鼠催眠活性的影响。两种非选择性NO合成酶抑制剂:N(G)-硝基- l -精氨酸甲酯(L-NAME)、N(G)-硝基- l -精氨酸(L-NOARG)和选择性NO合成酶抑制剂7-硝基茚唑(7-NI)均可显著增加地西泮、氯二氮环氧化物和氯硝西泮诱导睡眠的持续时间。l -精氨酸是一氧化氮形成的底物,与苯二氮卓类药物共同施用抑制剂的效果没有改变。单独服用l -精氨酸对苯二氮卓类药物诱导的睡眠时间没有影响。鸟腈环化酶抑制剂亚甲基蓝能够延长苯二氮卓类药物诱导的睡眠时间。这些发现提示cGMP/NO系统可能参与了苯二氮卓类药物的催眠作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Involvement of nitricoxidergic system in the hypnotic effects of benzodiazepines in mice.

The influence of nitric oxide (NO) on hypnotic activity of diazepam, chlordiazepoxide and clonazepam was studied in mice. Administration of both non-selective NO synthase inhibitors: N(G)-nitro-L-arginine methyl ester (L-NAME), N(G)-nitro-L-arginine (L-NOARG) and selective NO synthase inhibitor 7-nitroindazole (7-NI) resulted in significant increase in the duration of diazepam-, chlordiazepoxide- and clonazepam-induced sleep. The effects of co-administration of the examined inhibitors with benzodiazepines were not changed by L-arginine, a substrate for NO formation. Administration of L-arginine alone had no effect on the duration of sleep induced by benzodiazepines. Methylene blue, the guanyl cyclase inhibitor, was able to increase the duration of benzodiazepine-induced sleep. These findings suggest that the cGMP/NO system may participate in hypnotic effects of benzodiazepines.

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