Collins R C, Mehta S
Brain Res. 1978 Nov 24;157(2):311-20. doi: 10.1016/0006-8993(78)90033-1.
The biochemical and behavioral effects of the anticonvulsant amino-oxyacetic acid (AOAA) have been studied in a model of focal penicillin seizures in rats. At 20 mg/Kg AOAA treatment results in a progressive 11 fold increase in GABA levels in cortex over three hours. There is a decrease in aspartate, ketoglutarate, alanine and glutamine, and an initial decrease followed by an increase in pyruvate and glutamate. These results reflect a functional inhibition of several B-6 dependent aminotransferase enzymes. When rats are pretreated 30 min before the onset of focal penicillin seizures there is a 60% reduction in the number of discharges and a 34% reduction in seizure duration. Pretreatment beyond 75 min results in progressively less anticonvulsant effect, such that seizures eventually become more severe than control. There is an increase in the number and duration of discharges, seizure spikes become complex, and tonic-clonic events develop. Penicillin seizures do not cause a change in levels of GABA, but result in a decrease in glutamate within the focus. AOAA pretreatment initially prevents this decrease in glutamate but later accentuates it. The biochemical effects of AOAA are complex, but biphasic anticonvulsant properties coincide in time with a change in the balance of excitatory and inhibitory amino acids in the seizure focus.
抗惊厥药氨基氧乙酸(AOAA)的生化和行为学效应已在大鼠局灶性青霉素惊厥模型中进行了研究。以20mg/Kg的剂量给予AOAA治疗,会使皮质中的γ-氨基丁酸(GABA)水平在三小时内逐渐升高11倍。天冬氨酸、酮戊二酸、丙氨酸和谷氨酰胺的含量有所下降,丙酮酸和谷氨酸含量则先下降后上升。这些结果反映了几种依赖维生素B6的转氨酶的功能受到抑制。当在局灶性青霉素惊厥发作前30分钟对大鼠进行预处理时,放电次数减少60%,惊厥持续时间缩短34%。预处理超过75分钟后,抗惊厥作用逐渐减弱,以至于惊厥最终比对照组更严重。放电次数和持续时间增加,惊厥棘波变得复杂,并出现强直阵挛性发作。青霉素惊厥不会导致GABA水平改变,但会使病灶内的谷氨酸含量降低。AOAA预处理最初可防止谷氨酸含量降低,但随后会使其加剧。AOAA的生化效应较为复杂,但其双相抗惊厥特性与惊厥病灶中兴奋性和抑制性氨基酸平衡的变化在时间上相吻合。