Raiteri M, Costa R, Marchi M
Istituto di Farmacologia e Farmacognosia, Università degli Studi di Genova, Italy.
Neurosci Lett. 1992 Sep 28;145(1):109-13. doi: 10.1016/0304-3940(92)90215-s.
The effects of the nootropic drug oxiracetam on the K(+)-evoked overflow of [3H]D-aspartic acid ([3H]D-ASP), [3H]acetylcholine ([3H]ACh), [3H] gamma-aminobutyric acid ([3H]GABA), [3H]noradrenaline ([3H]NA) and [3H]5-hydroxytryptamine ([3H]5-HT) have been studied in superfused rat hippocampal slices. The overflow of [3H]D-ASP was enhanced by low concentrations of oxiracetam (0.01-1 microM) but not by high concentrations (10-100 microM) which showed some tendency to inhibit it. Similarly, low concentrations of oxiracetam increased, although less effectively, the depolarization-evoked overflow of [3H]ACh, whereas higher concentrations were without effect. At the concentrations active on [3H]D-ASP and [3H]ACh overflow oxiracetam did not affect that of [3H]GABA, [3H]NA or [3H]5-HT. The oxiracetam effects present in slices could not be observed in hippocampal synaptosomes. Thus oxiracetam may selectively increase the release of glutamate and acetylcholine in hippocampus by a mechanism which appears not to be sited in the releasing nerve terminals.
已在体外灌流的大鼠海马切片中研究了促智药奥拉西坦对钾离子诱发的[3H]D-天冬氨酸([3H]D-ASP)、[3H]乙酰胆碱([3H]ACh)、[3H]γ-氨基丁酸([3H]GABA)、[3H]去甲肾上腺素([3H]NA)和[3H]5-羟色胺([3H]5-HT)释放的影响。低浓度(0.01 - 1微摩尔)的奥拉西坦可增强[3H]D-ASP的释放,但高浓度(10 - 100微摩尔)则无此作用,反而有一定的抑制倾向。同样,低浓度的奥拉西坦虽效果稍差,但也能增加去极化诱发的[3H]ACh释放,而高浓度则无作用。在对[3H]D-ASP和[3H]ACh释放有活性的浓度下,奥拉西坦不影响[3H]GABA、[3H]NA或[3H]5-HT的释放。在海马突触体中未观察到切片中存在的奥拉西坦效应。因此,奥拉西坦可能通过一种似乎并非位于释放神经末梢的机制,选择性地增加海马中谷氨酸和乙酰胆碱的释放。