Floran B, Floran L, Sierra A, Aceves J
Departamento de Fisiología Biofísica y Neurociencias, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Mexico City, Mexico.
Neurosci Lett. 1997 Nov 14;237(1):1-4. doi: 10.1016/s0304-3940(97)00784-2.
Attempting to better understand the role of the dopaminergic innervation in the rat globus pallidus, we examined here whether or not endogenous dopamine modulates the release of [3H]GABA in superfused pallidal slices. The superfusion medium contained elevated (15 mM) potassium. The release of endogenous dopamine was induced by the dopamine releaser drug, methamphetamine. Methamphetamine (100 microM) inhibited by 46% the release of [3H]GABA. Methamphetamine inhibition was completely blocked by reserpinization of the rats. It was also completely blocked by the D2 dopamine receptor antagonist sulpiride (10 microM). Sulpiride alone caused a 105% increase in GABA release. The increase was not observed in slices from reserpinized rats. Quinpirole (10 microM), a D2 dopamine receptor agonist, inhibited (43%) [3H]GABA release. The results suggest that endogenous dopamine exerts an inhibitory effect on GABA release in the rat globus pallidus. The effect is mediated by D2 receptors presumably located on striatopallidal axon terminals.
为了更好地理解多巴胺能神经支配在大鼠苍白球中的作用,我们在此研究内源性多巴胺是否调节了灌注的苍白球切片中[3H]GABA的释放。灌注培养基中含有升高的(15 mM)钾。内源性多巴胺的释放由多巴胺释放药物甲基苯丙胺诱导。甲基苯丙胺(100 microM)抑制了[3H]GABA释放的46%。大鼠经利血平化后,甲基苯丙胺的抑制作用被完全阻断。它也被D2多巴胺受体拮抗剂舒必利(10 microM)完全阻断。单独使用舒必利可使GABA释放增加105%。在经利血平化的大鼠切片中未观察到这种增加。D2多巴胺受体激动剂喹吡罗(10 microM)抑制了(43%)[3H]GABA的释放。结果表明,内源性多巴胺对大鼠苍白球中GABA的释放具有抑制作用。该作用由可能位于纹状体苍白球轴突终末的D2受体介导。