Singh N A, Bush L G, Gibb J W, Hanson G R
Department of Pharmacology and Toxicology, University of Utah, Salt Lake City 84112.
Eur J Pharmacol. 1990 Oct 23;187(3):337-44. doi: 10.1016/0014-2999(90)90361-9.
A role for N-methyl-D-aspartate (NMDA)-type glutamate receptors in mediating the dopaminergic regulation of neurotensin (NT) systems was observed in extrapyramidal and limbic structures. Blockade of the NMDA receptor with the non-competitive antagonist, MK801, prevented increases in striatal and nigral levels of NT following both single and multiple administrations of methamphetamine. Significant attenuation of the methamphetamine-induced changes in the striatal NT system were observed with MK801 doses as low as 0.01 mg/kg per dose. In contrast, administration of NMDA caused significant increases in both striatal and nigral NT. The NMDA-induced increase in striatal NT content, like that caused by methamphetamine, was blocked by MK801. The NT system associated with the nucleus accumbens responded in a similar manner in that MK801 (0.1 mg/kg per dose) totally blocked the methamphetamine-induced increases and NMDA administration elevated the NT levels in this structure. Since the methamphetamine-related changes in NT content have been previously shown to be due to increased activity at dopamine D1 receptors, these results strongly suggest that NMDA receptors play an important role in mediating the dopamine D1 regulation of neurotensin systems. Interestingly, the presence of MK801 had no impact on sulpiride-mediated changes in striatal NT levels, suggesting that the NMDA receptor is not linked with the dopamine D2 receptor regulation of NT pathways.
在外锥体系和边缘系统中观察到N-甲基-D-天冬氨酸(NMDA)型谷氨酸受体在介导多巴胺能对神经降压素(NT)系统的调节中发挥作用。用非竞争性拮抗剂MK801阻断NMDA受体,可防止单次和多次给予甲基苯丙胺后纹状体和黑质中NT水平的升高。低至0.01mg/kg每剂量的MK801剂量就能显著减弱甲基苯丙胺诱导的纹状体NT系统变化。相比之下,给予NMDA会导致纹状体和黑质中的NT显著增加。NMDA诱导的纹状体NT含量增加,与甲基苯丙胺引起的增加一样,被MK801阻断。与伏隔核相关的NT系统也有类似反应,即MK801(0.1mg/kg每剂量)完全阻断了甲基苯丙胺诱导的增加,而给予NMDA则提高了该结构中的NT水平。由于先前已证明与甲基苯丙胺相关的NT含量变化是由于多巴胺D1受体活性增加所致,这些结果强烈表明NMDA受体在介导多巴胺D1对神经降压素系统的调节中起重要作用。有趣的是,MK801的存在对舒必利介导的纹状体NT水平变化没有影响,这表明NMDA受体与NT途径的多巴胺D2受体调节无关。