Feenstra M G, van der Weij W, Botterblom M H
Netherlands Institute for Brain Research, Graduate School of Neurosciences Amsterdam.
Neurosci Lett. 1995 Dec 8;201(2):175-8. doi: 10.1016/0304-3940(95)12164-1.
Using microdialysis, the glutamate agonist N-methyl-D-aspartate (NMDA) was perfused for 20 min through the medial prefrontal cortex of freely moving rats, and its effects on extracellular concentrations of dopamine (DA) were determined. NMDA (1 mM) increased DA to 170-1500%, depending on the intensity and duration of the clonic forelimb jerks and convulsions that were induced. NMDA (0.1 mM), however, decreased DA to 61%. Metabolites of DA were decreased after both concentrations of NMDA. The effects of both 0.1 mM and 1 mM NMDA were blocked by 0.5 mM of the competitive NMDA-antagonist D-AP-5. The NMDA-induced decrease in release and metabolism possibly results from an indirect action via an inhibitory local interneuron or polysynaptic circuit.
采用微透析技术,将谷氨酸激动剂N-甲基-D-天冬氨酸(NMDA)灌注自由活动大鼠的内侧前额叶皮质20分钟,并测定其对细胞外多巴胺(DA)浓度的影响。NMDA(1 mM)可使DA增加至170% - 1500%,具体增幅取决于所诱发的阵挛性前肢抽搐和惊厥的强度及持续时间。然而,NMDA(0.1 mM)可使DA降低至61%。两种浓度的NMDA均可使DA的代谢产物减少。0.5 mM竞争性NMDA拮抗剂D-AP-5可阻断0.1 mM和1 mM NMDA的作用。NMDA诱导的释放和代谢减少可能是通过抑制性局部中间神经元或多突触回路产生的间接作用所致。