Erden B F, Ulak G, Yildiran G, Gacar N
Kocaeli University, Faculty of Medicine, Department of Pharmacology, Turkey.
Pharmacol Res. 1997 Oct;36(4):265-7. doi: 10.1006/phrs.1997.0185.
The sleep-wakefulness continuity is sensitive to a wide range of agents with pharmacological activity. There is some strong evidence about the role of nitric oxide (NO) as an intercellular messenger in the central physiological mechanisms. The effects of 7-nitro indazole (7-NI 15, 30, 60 mg kg-1; intraperitoneal, i.p.), a selective inhibitor of neuronal nitric oxide synthase (NOS) and L-arginine (500, 1000 mg kg-1, i.p.), a NO precursor, on pentobarbital (35 mg kg-1, i.p.) sleep were examined in mice. Loss of the righting reflex was used to determine the start of sleep. Sleep latency and sleeping time were evaluated in each experiment. 7-Nitro indazole (7-NI 30 mg kg-1; i.p.), had no apparent effect on sleep latency but significantly increased sleeping time (P < 0.02) on pentobarbital sleep in mice. L-Arginine had no effect on both parameters. These findings suggest that NO might be an important modulator of sleep regulation and implicate that inhibition of release and/or synthesis of NO might lead to changes in the maintenance of sleep.
睡眠 - 觉醒连续性对多种具有药理活性的物质敏感。有一些有力证据表明一氧化氮(NO)作为细胞间信使在中枢生理机制中发挥作用。研究了7 - 硝基吲唑(7 - NI,15、30、60毫克/千克;腹腔注射,i.p.),一种神经元型一氧化氮合酶(NOS)的选择性抑制剂,以及L - 精氨酸(500、1000毫克/千克,i.p.),一种NO前体,对小鼠戊巴比妥(35毫克/千克,i.p.)诱导睡眠的影响。以翻正反射消失来确定睡眠开始。在每个实验中评估睡眠潜伏期和睡眠时间。7 - 硝基吲唑(7 - NI,30毫克/千克;i.p.)对小鼠戊巴比妥诱导睡眠的睡眠潜伏期无明显影响,但显著增加睡眠时间(P < 0.02)。L - 精氨酸对这两个参数均无影响。这些发现表明NO可能是睡眠调节的重要调节因子,并暗示抑制NO的释放和/或合成可能导致睡眠维持的改变。