Balcar V J, Mandel P
Experientia. 1976;32(7):904-5. doi: 10.1007/BF02003758.
Several branched fatty acids including an antiepileptic agent nDPA were tested as potential inhibitors of high affinity uptake of GABA by brain slices and synaptosomes. Only three compounds (2-butyl-3-propylhexanoic acid, 5-propyloctanoic acid, 2-propylpenten-2-oic acid) were found to be relatively weak inhibitors of the uptake system. There was no correlation between anticonvulsant properties of the branched fatty acids and their potencies as inhibitors of high affinity uptake of GABA.
包括抗癫痫药物nDPA在内的几种支链脂肪酸作为脑片和突触体对GABA高亲和力摄取的潜在抑制剂进行了测试。仅发现三种化合物(2-丁基-3-丙基己酸、5-丙基辛酸、2-丙基戊-2-烯酸)是摄取系统相对较弱的抑制剂。支链脂肪酸的抗惊厥特性与其作为GABA高亲和力摄取抑制剂的效力之间没有相关性。