Kubová H, Mares P
Faculty of Pharmacy, Charles University, Hradec Králové, Czechoslovakia.
Arch Int Pharmacodyn Ther. 1989 May-Jun;299:35-43.
The action of clonazepam (CZP) against after-discharges (ADs) induced by perforant path stimulation was studied in 11 rats with implanted electrodes. The animals passed 4 sessions: one control, one with the solvent injection, and two with the administration of CZP (either 0.1 or 1 mg/kg i.p.). The ADs were always induced 4 times with 20 min intervals, the injections took place 10 min before the second stimulation. The EEG pattern of ADs was not changed by either dose of CZP and the duration was transiently shortened by the high dose only. Incidence of recurrent ADs tended to decrease after the lower dose of CZP, the higher dose blocked them for at least 30 min. As concerns behavioral concomitants of ADs, wet dog shakes remained uninfluenced by CZP while orienting reaction was either fully blocked (by the high dose of CZP) or significantly suppressed (by the lower dose).
在11只植入电极的大鼠中研究了氯硝西泮(CZP)对穿孔通路刺激诱导的后放电(ADs)的作用。这些动物经历了4个阶段:一个对照阶段、一个注射溶剂的阶段以及两个给予CZP(腹腔注射,剂量为0.1或1mg/kg)的阶段。总是以20分钟的间隔诱导ADs 4次,在第二次刺激前10分钟进行注射。两种剂量的CZP均未改变ADs的脑电图模式,仅高剂量短暂缩短了其持续时间。低剂量的CZP使复发性ADs的发生率趋于降低,高剂量则至少阻断30分钟。关于ADs的行为伴随症状,“湿狗样抖动”不受CZP影响,而定向反应要么被高剂量的CZP完全阻断,要么被低剂量显著抑制。