Ohmori T, Koyama T, Yamashita I
Department of Psychiatry and Neurology, Hokkaido University School of Medicine, Sapporo, Japan.
Life Sci. 1991;48(3):283-9. doi: 10.1016/0024-3205(91)90356-g.
Endogenous dopamine (DA) and norepinephrine (NE) in the superfusate from slices of rat medial prefrontal cortex were measured by high-performance liquid chromatography coupled to electrochemical detection (HPLC-ECD). Stimulation with high K+ or methamphetamine (MAP) evoked a dose-dependent elevation in the release of DA and NE, although spontaneous release of DA or NE was barely detectable. The K(+)-evoked release was Ca++ dependent, whereas the MAP-evoked release was not. The K(+)-evoked DA release was inhibited by the DA agonist apomorphine (1 microM or 10 microM) and enhanced by the D2 antagonist (-)-sulpiride (1 microM). The K(+)-evoked NE release was inhibited by the alpha-2 agonist clonidine (0.1 microM or 1 microM) and enhanced by the alpha-2 antagonist idazoxan (1 microM). These results confirm the existence of release modulatory D2 and alpha-2 receptors in the medial prefrontal cortex. The present study is the first description of a method which allows evaluation of the release of endogenous DA or NE in the cortex slices and is competent to examine the properties of the two catecholamines release and their regulation by presynaptic receptors.
采用高效液相色谱-电化学检测法(HPLC-ECD)测定大鼠内侧前额叶皮质切片灌流液中的内源性多巴胺(DA)和去甲肾上腺素(NE)。高钾或甲基苯丙胺(MAP)刺激可引起DA和NE释放呈剂量依赖性升高,尽管几乎检测不到DA或NE的自发释放。钾离子诱发的释放依赖于钙离子,而MAP诱发的释放则不依赖。钾离子诱发的DA释放受到DA激动剂阿扑吗啡(1微摩尔或10微摩尔)的抑制,并被D2拮抗剂(-)-舒必利(1微摩尔)增强。钾离子诱发的NE释放受到α2激动剂可乐定(0.1微摩尔或1微摩尔)的抑制,并被α2拮抗剂咪唑克生(1微摩尔)增强。这些结果证实了内侧前额叶皮质中存在释放调节性D2和α2受体。本研究首次描述了一种可评估皮质切片中内源性DA或NE释放,并能检测两种儿茶酚胺释放特性及其受突触前受体调节情况的方法。