Mendelson W B
Department of Neurology, Cleveland Clinic Foundation, Ohio 44195.
Neuropsychopharmacology. 1994 May;10(3):151-5. doi: 10.1038/npp.1994.17.
In previous studies, the author has reported both in vitro and in vivo sleep studies in which there were complex interactions between benzodiazepine hypnotics and the dihydropyridine calcium channel blocker nifedipine. The author has also reported that microinjections of triazolam into the dorsal raphe nucleus of the rat result in enhancement of wakefulness. In the present study, nifedipine and triazolam were coadministered into this site. As previously was observed, triazolam produced a dose-dependent increase in sleep latency and a decrease in total sleep, primarily by reducing non-rapid-eye-movement sleep. Nifedipine had no effect on sleep when given by itself but prevented the alterations in sleep by triazolam. These various sleep effects were not associated with alterations in core temperature. These data are consistent with the view that aspect of the sleep-altering activity of triazolam involves interaction with voltage-dependent calcium channel activity.
在先前的研究中,作者报道了苯二氮䓬类催眠药与二氢吡啶类钙通道阻滞剂硝苯地平之间存在复杂相互作用的体外和体内睡眠研究。作者还报道,向大鼠中缝背核微量注射三唑仑会导致觉醒增强。在本研究中,硝苯地平和三唑仑同时注射到该部位。如先前观察到的,三唑仑主要通过减少非快速眼动睡眠,使睡眠潜伏期呈剂量依赖性增加,总睡眠时间减少。硝苯地平单独给药时对睡眠无影响,但可防止三唑仑引起的睡眠改变。这些不同的睡眠效应与核心体温的改变无关。这些数据与以下观点一致,即三唑仑改变睡眠活动的某些方面涉及与电压依赖性钙通道活性的相互作用。