Meldrum B S, Horton R W
Psychopharmacology (Berl). 1979 Feb 28;60(3):277-80. doi: 10.1007/BF00426668.
Two new 1,5 benzodiazepines have been evaluated acutely as anticonvulsants in baboons, Papio papio, with photosensitive epilepsy. BAU 426 (8-Chlor-6-[2-chlorphenyl]-4H-s-triazolo-[4,3-a] [1,5-benzodiazepin-5-[6-H]on) and BAU 500 (analogue of BAU 426 with [2-trifluor methylphenyl] substituted for [2-chlorphenyl]), 0.1--5.0 mg/kg, were administered i.v. to baboons with and without priming with D,L allylglycine. BAU 426 or BAU 500, 0.1--0.2 mg/kg, produced partial or transient protection against photically induced myoclonus or epileptic responses. Complete protection, in the absence of signs of sedation or acute neurological toxicity, was seen 1--4 h after 0.5--2 mg/kg. EEG changes typical of benzodiazepines were seen for 1--3 h and clinical signs of sedation with some muscular hypotonia were evident for 1 h after either drug, 5 mg/kg. Clinical trials are required to determine if these compounds are superior to 1,4 benzodiazepines as anticonvulsants.
两种新型1,5 - 苯二氮䓬类药物已在患有光敏性癫痫的狒狒(豚尾狒狒)身上进行了急性抗惊厥评估。BAU 426(8 - 氯 - 6 - [2 - 氯苯基] - 4H - s - 三唑并[4,3 - a] [1,5 - 苯二氮䓬 - 5 - [6 - H]酮)和BAU 500(BAU 426的类似物,其中[2 - 氯苯基]被[2 - 三氟甲基苯基]取代),剂量为0.1 - 5.0毫克/千克,通过静脉注射给予有或没有用D,L - 烯丙基甘氨酸预处理的狒狒。BAU 426或BAU 500,剂量为0.1 - 0.2毫克/千克,对光诱导的肌阵挛或癫痫反应产生部分或短暂的保护作用。在给予0.5 - 2毫克/千克药物后1 - 4小时,可观察到完全保护作用,且无镇静或急性神经毒性迹象。给予5毫克/千克任何一种药物后,苯二氮䓬类典型的脑电图变化持续1 - 3小时,镇静的临床体征伴有一些肌肉张力减退在给药后1小时明显。需要进行临床试验以确定这些化合物作为抗惊厥药是否优于1,4 - 苯二氮䓬类药物。