Kim J H, Vezina P
Department of Psychiatry, University of Chicago, Illinois, USA.
J Pharmacol Exp Ther. 1998 Jan;284(1):317-22.
This study examined the role played by metabotropic glutamate receptors in the nucleus accumbens in dopamine agonist-induced locomotion. Rats received microinjections into this nucleus of the selective metabotropic glutamate receptor antagonist, (RS)-alpha-methyl-4-carboxyphenylglycine, alone or with amphetamine and their locomotor activity was subsequently measured for 2 hr. None of the doses of (RS)-alpha-methyl-4-carboxyphenylglycine tested (0.025, 0.25, 2.5, or 25 nmol/0.5 microliter/side) when administered alone produced effects on locomotion that differed significantly from those observed after saline. However, when co-injected with amphetamine (6.8 nmol [2.5 micrograms]/side) into the nucleus accumbens, a moderately high dose of (RS)-alpha-methyl-4-carboxyphenylglycine (25 nmol/side) completely blocked, whereas a lower dose (0.25 nmol/side) potentiated the locomotor effects of amphetamine. (RS)-alpha-Methyl-4-carboxyphenylglycine (25 nmol/side) also blocked the locomotor-activating effects of apomorphine (32.9 nmol [10 micrograms]/side), when co-injected with this direct dopamine receptor agonist into the nucleus accumbens. These results suggest that metabotropic glutamate receptors in the nucleus accumbens contribute to amphetamine-induced locomotion and that this contribution may be mediated, at least in part, by metabotropic glutamate receptors expressed by intrinsic nucleus accumbens cells located postsynaptic to dopamine neuron terminals.
本研究考察了伏隔核中代谢型谷氨酸受体在多巴胺激动剂诱导的运动中所起的作用。大鼠被微注射选择性代谢型谷氨酸受体拮抗剂(RS)-α-甲基-4-羧基苯甘氨酸至该核,单独注射或与苯丙胺一起注射,随后测量它们2小时的运动活性。单独注射时,所测试的(RS)-α-甲基-4-羧基苯甘氨酸的任何剂量(0.025、0.25、2.5或25 nmol/0.5微升/侧)对运动产生的影响与注射生理盐水后观察到的影响相比均无显著差异。然而,当与苯丙胺(6.8 nmol[2.5微克]/侧)共同注射到伏隔核时,中等高剂量的(RS)-α-甲基-4-羧基苯甘氨酸(25 nmol/侧)完全阻断了苯丙胺的运动效应,而较低剂量(0.25 nmol/侧)则增强了苯丙胺的运动效应。当与直接多巴胺受体激动剂阿扑吗啡(32.9 nmol[10微克]/侧)共同注射到伏隔核时,(RS)-α-甲基-4-羧基苯甘氨酸(25 nmol/侧)也阻断了阿扑吗啡的运动激活效应。这些结果表明,伏隔核中的代谢型谷氨酸受体促成了苯丙胺诱导的运动,并且这种促成作用可能至少部分地由位于多巴胺神经元终末突触后、伏隔核固有细胞所表达的代谢型谷氨酸受体介导。