Kuhn F J, Böke-Kuhn K, Danneberg P, Lehr E, Stockhaus K
Br J Clin Pharmacol. 1983;16 Suppl 2(Suppl 2):253S-260S. doi: 10.1111/j.1365-2125.1983.tb02297.x.
Brotizolam differs in pharmacological profile from other diazepines by virtue of its hypnogenic potency. It increases, whereas other diazepines reduce, sleep in the cat. With increasing doses, the latency to rapid eye movement sleep is lengthened and the proportion is reduced. Brotizolam has anxiolytic, anticonvulsant and muscle relaxant properties. The effective anxiolytic and muscle relaxant doses are somewhat lower than those of diazepam, and the effective anti-convulsant dose is ten times lower. Barbiturate synergism in mice is lower with brotizolam than with diazepam, while alcohol-induced coma is prolonged over the same dose range. Side-effects of brotizolam are similar to those of other diazepines, but the therapeutic range is more favourable. Physical dependence as tested in the monkey seems to be low.
溴替唑仑因其催眠效力在药理学特性上与其他苯二氮䓬类药物不同。它能增加猫的睡眠时间,而其他苯二氮䓬类药物则会减少。随着剂量增加,快速眼动睡眠的潜伏期延长且比例降低。溴替唑仑具有抗焦虑、抗惊厥和肌肉松弛特性。其有效的抗焦虑和肌肉松弛剂量略低于地西泮,而有效的抗惊厥剂量则低十倍。在小鼠中,溴替唑仑的巴比妥类协同作用低于地西泮,而在相同剂量范围内,酒精诱导的昏迷时间会延长。溴替唑仑的副作用与其他苯二氮䓬类药物相似,但治疗范围更有利。在猴子身上测试的身体依赖性似乎较低。