Rimmer E M, Milligan N M, Richens A
Department of Pharmacology, University of Wales College of Medicine, Heath Park, Cardiff, U.K.
Epilepsy Res. 1987 Nov-Dec;1(6):339-46. doi: 10.1016/0920-1211(87)90058-1.
The acute effect of oral administration of a single dose of vigabatrin, a new antiepileptic drug which acts by irreversible enzyme-activated inhibition of the brain enzyme, GABA-aminotransferase, on the photoconvulsive response in patients with photosensitive epilepsy, was compared with that of the established antiepileptic drug, sodium valproate. Both drugs significantly suppressed the photoconvulsive response in 3 out of 6 subjects. This result was interpreted as further evidence of vigabatrin's potential value in the future treatment of patients with epilepsy.
将单剂量的氨己烯酸(一种新型抗癫痫药物,通过不可逆地酶激活抑制脑内酶γ-氨基丁酸转氨酶发挥作用)口服给药,对光敏性癫痫患者光惊厥反应的急性影响,与已有的抗癫痫药物丙戊酸钠进行了比较。两种药物均使6名受试者中的3名的光惊厥反应得到显著抑制。这一结果被解释为氨己烯酸在未来癫痫患者治疗中潜在价值的进一步证据。