Schechter P J, Tranier Y, Jung M J, Böhlen P
Eur J Pharmacol. 1977 Oct 15;45(4):319-28. doi: 10.1016/0014-2999(77)90270-9.
gamma-Acetylenic GABA and gamma-vinyl GABA, two catalytic irreversible inhibitors of GABA-transaminase, produce marked and sustained elevations in mouse brain GABA concentrations and protect DBA/2 mice against audiogenically induced seizures in a similar dose and time-dependent manner. The acetylenic analog also inhibits GAD activity while the vinyl compound has minimal activity against this enzyme. The increase in brain GABA concentrations induced by these compounds correlates well with attenuation of audiogenic seizure intensity (r = 0.991 and 0.962 for gamma-acetylenic and gamma-vinyl GABA respectively) and with degree of seizure protection (r = 0.974 and 0.834). Seizure intensity is reduced by 50% when brain GABA is increased to 265% and 264% of control values by the two inhibitors and seizure incidence is halved at 322% and 324%. Thus, audiogenic seizure protection in genetically susceptible mice is apparently a function of whole brain GABA concentrations.
γ-乙炔基 GABA 和 γ-乙烯基 GABA 是 GABA 转氨酶的两种催化不可逆抑制剂,它们能使小鼠脑内 GABA 浓度显著且持续升高,并以相似的剂量和时间依赖性方式保护 DBA/2 小鼠免受听源性惊厥。炔基类似物还抑制谷氨酸脱羧酶(GAD)活性,而乙烯基化合物对该酶的活性极小。这些化合物诱导的脑内 GABA 浓度升高与听源性惊厥强度的减弱密切相关(γ-乙炔基 GABA 和 γ-乙烯基 GABA 的相关系数分别为 0.991 和 0.962),也与惊厥保护程度相关(相关系数分别为 0.974 和 0.834)。当脑内 GABA 被这两种抑制剂分别升高至对照值的 265%和 264%时,惊厥强度降低 50%;当脑内 GABA 升高至对照值的 322%和 324%时,惊厥发生率减半。因此,在基因易感性小鼠中,听源性惊厥保护显然是全脑 GABA 浓度的函数。