Shimizu H, Hirose A, Tatsuno T, Nakamura M, Katsube J
Research Laboratories, Sumitomo Pharmaceuticals Co., Ltd., Osaka, Japan.
Jpn J Pharmacol. 1987 Dec;45(4):493-500. doi: 10.1254/jjp.45.493.
Pharmacological properties of SM-3997 (3a alpha,4 beta,7 beta,7a alpha-hexahydro-2-(4-(4-(2-pyrimidinyl)-1- piperazinyl)-butyl)-4,7-methano-1H-isoindole-1,3(2H)-dione dihydrogen citrate) have been examined in rats and mice. SM-3997 showed a dose-related anticonflict activity in rats in a water lick conflict paradigm, and it had no effect on water consumption in a spontaneous water drinking test. The potency of SM-3997 appeared to be equal to that of buspirone and about one-half that of diazepam. No tolerance to the anticonflict activity of SM-3997 was observed following 5 and 10 consecutive days of treatment. Unlike diazepam, SM-3997 had no anticonvulsant effect and had very weak muscle relaxant and hypnotic effects. On the other hand, SM-3997 and buspirone exhibited dopamine antagonistic action, although the potency of SM-3997 was less than one fourth that of buspirone. These results show that SM-3997 is a new anxioselective anxiolytic agent which is weaker than buspirone in the dopaminergic neuron system.
已在大鼠和小鼠中对SM - 3997(3aα,4β,7β,7aα - 六氢 - 2 -(4 -(4 -(2 - 嘧啶基) - 1 - 哌嗪基) - 丁基) - 4,7 - 亚甲基 - 1H - 异吲哚 - 1,3(2H) - 二酮二氢柠檬酸盐)的药理特性进行了研究。在舔水冲突范式中,SM - 3997在大鼠中表现出剂量相关的抗冲突活性,并且在自发饮水试验中对水消耗没有影响。SM - 3997的效力似乎与丁螺环酮相当,约为地西泮的一半。连续治疗5天和10天后,未观察到对SM - 3997抗冲突活性的耐受性。与地西泮不同,SM - 3997没有抗惊厥作用,肌肉松弛和催眠作用非常弱。另一方面,SM - 3997和丁螺环酮表现出多巴胺拮抗作用,尽管SM - 3997的效力小于丁螺环酮的四分之一。这些结果表明,SM - 3997是一种新型的抗焦虑选择性抗焦虑药,在多巴胺能神经元系统中比丁螺环酮弱。