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N-甲基-D-天冬氨酸(NMDA)受体阻断可减弱纹状体内多巴胺D1受体刺激所引发的运动。

NMDA receptor blockade attenuates locomotion elicited by intrastriatal dopamine D1-receptor stimulation.

作者信息

Kreipke Christian W, Walker Paul D

机构信息

Cellular and Clinical Neurobiology Program, Department of Psychiatry and Behavioral Neurosciences, Wayne State University School of Medicine, Detroit, Michigan 48201, USA.

出版信息

Synapse. 2004 Jul;53(1):28-35. doi: 10.1002/syn.20035.

Abstract

Previous behavioral studies suggest that the striatum mediates a hyperactive response to systemic NMDA receptor antagonism in combination with systemic D1 receptor stimulation. However, many experiments conducted at the cellular level suggest that inhibition of NMDA receptors should block D1 receptor-mediated locomotor activity. Therefore, we investigated the consequences of NMDA receptor blockade on the ability of striatal D1 receptors to elicit locomotor activity using systemic and intrastriatal injections of the NMDA antagonist MK-801 combined with intrastriatal injections of the D1 full agonist SKF 82958. Following drug treatment locomotor activity was measured via computerized activity monitors designed to quantify multiple parameters of rodent open-field behavior. Both systemic (0.1 mg/kg) and intrastriatal (1.0 microg) MK-801 pretreatments completely blocked locomotor and stereotypic activity elicited by 10 microg of SKF 82958 directly infused into the striatum. Further, increased activity triggered by intrastriatal SKF 82958 was attenuated by a posttreatment with intrastriatal infusion of 1 microg MK-801. These data suggest that D1-stimulated locomotor behaviors controlled by the striatum require functional NMDA channels.

摘要

先前的行为学研究表明,纹状体介导了对全身NMDA受体拮抗作用与全身D1受体刺激相结合的过度活跃反应。然而,许多在细胞水平进行的实验表明,抑制NMDA受体会阻断D1受体介导的运动活性。因此,我们使用NMDA拮抗剂MK-801的全身和纹状体内注射结合纹状体内注射D1完全激动剂SKF 82958,研究了NMDA受体阻断对纹状体D1受体引发运动活性能力的影响。药物处理后,通过设计用于量化啮齿动物旷场行为多个参数的计算机化活动监测器测量运动活性。全身(0.1mg/kg)和纹状体内(1.0μg)MK-801预处理均完全阻断了直接注入纹状体的10μg SKF 82958引发的运动和刻板行为。此外,纹状体内注射SKF 82958引发的活动增加被纹状体内注入1μg MK-801的后处理减弱。这些数据表明,纹状体控制的D1刺激的运动行为需要功能性NMDA通道。

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