Morrow B A, Clark W A, Roth R H
Yale University School of Medicine, Department of Pharmacology and Psychiatry, New Haven, CT 06510.
Eur J Pharmacol. 1993 Jul 20;238(2-3):255-62. doi: 10.1016/0014-2999(93)90855-c.
Restraint of brief duration causes a metabolic activation of mesocortical and some mesolimbic dopaminergic systems with little effect on the nigrostriatal system. We have examined the ability of an antagonist of the allosteric glycine site of the N-methyl-D-aspartate receptor complex to block the stress-induced response in dopamine utilization. Thirty minutes of restraint stress elevated dopamine metabolism, as measured by the ratio between 3,4-dihydroxyphenylacetic acid (DOPAC) and dopamine, in both the medial prefrontal cortex and nucleus accumbens. An antagonist for the glycine/N-methyl-D-aspartate receptor complex, 1-hydroxy-3-aminopyrrolidone-2 ((+)-HA-966), given systemically or injected into the ventral tegmental area, prevents the stress-induced increase in dopamine metabolism in the prefrontal cortex without altering the response in the nucleus accumbens. Similarly, systemic administration of the non-competitive antagonist for the N-methyl-D-aspartate receptor, dizocilpine ((+)-MK-801), blocked the stress-induced rise in dopamine metabolism in the medial prefrontal cortex but not the nucleus accumbens. The negative enantiomer of HA-966 did not produce a selective antagonism of the stress-induced dopamine metabolism in the medial prefrontal cortex. These results support previous work which suggest the mesocortical and mesoaccumbens dopamine neurons respond to excitatory input through different glutamate receptor mechanisms. Additionally, the specific blockade of the stress-induced change in dopamine metabolism in the medial prefrontal cortex by a glycine antagonist implies a role for such an antagonist in treatment of disease states which may involve disruptions of N-methyl-D-aspartate receptor function.
短时间的束缚会引起中皮质和一些中脑边缘多巴胺能系统的代谢激活,而对黑质纹状体系统影响很小。我们研究了N-甲基-D-天冬氨酸受体复合物变构甘氨酸位点拮抗剂阻断应激诱导的多巴胺利用反应的能力。通过3,4-二羟基苯乙酸(DOPAC)与多巴胺的比率测量,30分钟的束缚应激使内侧前额叶皮质和伏隔核中的多巴胺代谢升高。甘氨酸/N-甲基-D-天冬氨酸受体复合物的拮抗剂1-羟基-3-氨基吡咯烷-2((+)-HA-966)全身给药或注射到腹侧被盖区,可防止应激诱导的前额叶皮质多巴胺代谢增加,而不会改变伏隔核中的反应。同样,N-甲基-D-天冬氨酸受体的非竞争性拮抗剂地佐环平((+)-MK-801)全身给药可阻断应激诱导的内侧前额叶皮质多巴胺代谢升高,但不能阻断伏隔核中的升高。HA-966的负对映体不会对内侧前额叶皮质应激诱导的多巴胺代谢产生选择性拮抗作用。这些结果支持了先前的研究工作,表明中皮质和中伏隔核多巴胺神经元通过不同的谷氨酸受体机制对兴奋性输入作出反应。此外,甘氨酸拮抗剂对内侧前额叶皮质应激诱导的多巴胺代谢变化的特异性阻断意味着这种拮抗剂在治疗可能涉及N-甲基-D-天冬氨酸受体功能破坏的疾病状态中具有作用。