Tarazi F I, Zhang K, Baldessarini R J
Mailman Research Center, McLean Division of Massachusetts General Hospital, 115 Mill Street, Belmont, MA 02478, USA.
Brain Res. 2000 Oct 20;881(1):69-72. doi: 10.1016/s0006-8993(00)02812-2.
Changes in ionotropic glutamate NMDA, AMPA and KA receptor binding in rat caudate-putamen were examined by quantitative in vitro receptor autoradiography 5 weeks after lesioning nigrostriatal dopaminergic projections. In this animal model of Parkinson's disease, density of binding in caudate-putamen increased at KA, but not NMDA or AMPA receptors. The findings indicate that nigrostriatal dopamine denervation can selectively enhance KA receptor levels in rat basal ganglia, suggest that KA receptors contribute to the pathophysiology of Parkinson's disease, and may suggest innovative treatments.
在损毁黑质纹状体多巴胺能投射5周后,通过定量体外受体放射自显影术检测大鼠尾状核-壳核中离子型谷氨酸NMDA、AMPA和KA受体结合的变化。在这个帕金森病动物模型中,尾状核-壳核中KA受体的结合密度增加,但NMDA或AMPA受体的结合密度未增加。这些发现表明,黑质纹状体多巴胺去神经支配可选择性增强大鼠基底神经节中KA受体水平,提示KA受体参与帕金森病的病理生理过程,并可能为创新治疗提供思路。