Masuda Y, Karasawa T, Shiraishi Y, Hori M, Yoshida K, Shimizu M
Arzneimittelforschung. 1980;30(3):477-83.
The anticonvulsant and neurotoxic properties of 3-sulfamoylmethyl-1,2-benzisoxazole (AD-810) have been demonstrated. AD-810 suppressed electrically and chemically induced maximal seizures but did not prevent minimal seizures in experimental animals. In rats, rabbits and dogs, the anticonvulsant activity of AD-810 against maximal electroshock seizures was more potent than those of diphenylhydantoin and carbamazepine. In rats, AD-810 showed more rapid onset as well as longer duration of anticonvulsant activity than the above two drugs. The anticonvulsant effect of AD-810 was reduced but not abolished by reserpine. No tolerance developed to the anticonvulsant action of AD-810 by consecutive treatment. The compound showed much less neurotoxicity and lethal toxicity than the existing antiepileptic drugs for grand mal, and also showed the least hypnotic effect by itself or by combination with hexobarbital. Thus, AD-810 possesses a profile of anticonvulsant activity most similar to that of diphenylhydantoin or carbamazepine, providing a high protective index as well as other favorable properties.
3-氨磺酰甲基-1,2-苯并异恶唑(AD-810)的抗惊厥和神经毒性特性已得到证实。AD-810可抑制电刺激和化学诱导的最大惊厥,但不能预防实验动物的最小惊厥。在大鼠、兔子和狗中,AD-810对最大电休克惊厥的抗惊厥活性比苯妥英钠和卡马西平更强。在大鼠中,AD-810的抗惊厥活性起效更快,持续时间也比上述两种药物更长。利血平可降低AD-810的抗惊厥作用,但未完全消除。连续给药未使机体对AD-810的抗惊厥作用产生耐受性。与现有的大发作抗癫痫药物相比,该化合物的神经毒性和致死毒性要小得多,并且单独使用或与己巴比妥联合使用时催眠作用也最小。因此,AD-810具有与苯妥英钠或卡马西平最为相似的抗惊厥活性特征,具有较高的保护指数以及其他有利特性。