Laboratorio di Biologia Cellulare, CNR, Rome.
Neurochem Res. 1976 Aug;1(4):409-16. doi: 10.1007/BF00966232.
The effects of the ionophore A23187 and of ouabain on the release of [(3)H]GABA and [(3)H]norepinephrine were studied in superfused rat brain synaptosomes. Each of the two drugs moderately stimulated the spontaneous release of [(3)H]GABA, but greatly potentiated the release of [(3)H]GABA induced by unlabeled GABA. In contrast, the ionophore and norepinephrine showed an additive, but not a "supraadditive," releasing effect on synaptosomal [(3)H]norepinephrine. Ouabain modestly and transiently potentiated the norepinephrine-induced [(3)H]norepinephrine release, which, however, was inhibited by the drug after a few minutes. It is suggested that in the new intrasynaptosomal ionic conditions determined by the two drugs, the stoichiometry of the basal homoexchange of GABA is changed in a direction favoring net outward transport.
在体外灌流的大鼠脑突触小体中研究了离子载体 A23187 和哇巴因对 [(3)H]GABA 和 [(3)H]去甲肾上腺素释放的影响。两种药物都适度刺激 [(3)H]GABA 的自发释放,但大大增强了未标记 GABA 诱导的 [(3)H]GABA 释放。相比之下,离子载体和去甲肾上腺素对突触小体 [(3)H]去甲肾上腺素释放表现出相加而非“超相加”的释放效应。哇巴因适度且短暂地增强了去甲肾上腺素诱导的 [(3)H]去甲肾上腺素释放,但几分钟后药物会抑制这种释放。因此,在这两种药物确定的新的突触内离子条件下,GABA 基本同型交换的化学计量比朝着有利于净外向转运的方向发生变化。