Yamamoto K, Sawada T, Utsumi S, Naito Y, Koshida H
Neuropharmacology. 1982 May;21(5):413-21. doi: 10.1016/0028-3908(82)90024-7.
Behavioral and electrophysiological comparative analyses of the effects of 2-o-chlorobenzoyl-4-chloro-N-methyl-N alpha-glycylglycinanilide hydrate (45-0088-S) and diazepam on the CNS were performed with cats and monkeys. No essential difference between 45-0088-S and diazepam on the effects in the CNS was observed, although the "taming" effect in wild cats and the hypnotic effect in monkeys caused by 45-0088-S were stronger than those of diazepam. The sleep-wakefulness cycles in both cats and monkeys were modified by 45-0088-S. The activity of the reticular formation, hypothalamus and amygdala in cats was inhibited by 45-0088-S and by diazepam.
采用猫和猴子对2 -邻氯苯甲酰基 - 4 -氯 - N -甲基 - Nα -甘氨酰甘氨酰苯胺水合物(45 - 0088 - S)和地西泮对中枢神经系统的影响进行了行为学和电生理学比较分析。尽管45 - 0088 - S对野猫的“驯服”作用和对猴子的催眠作用比地西泮更强,但未观察到45 - 0088 - S和地西泮在中枢神经系统作用方面的本质差异。45 - 0088 - S改变了猫和猴子的睡眠 - 觉醒周期。45 - 0088 - S和地西泮均抑制了猫的网状结构、下丘脑和杏仁核的活动。