McNamara Robert K, Logue Aaron, Stanford Kevin, Xu Ming, Zhang Jianhua, Richtand Neil M
Department of Psychiatry, University of Cincinnati College of Medicine, Cincinnati, Ohio 45267, USA.
Synapse. 2006 Oct;60(5):399-405. doi: 10.1002/syn.20315.
Accumulating evidence suggests that dopamine D3 receptor (D3R) stimulation is inhibitory to spontaneous and psychostimulant-induced locomotion through opposition of concurrent D1R and D2R-mediated signaling. To evaluate this model, we used homozygous D3R mutant mice and wild-type controls to investigate the role of the D3R in locomotor activity and stereotypy stimulated by acute amphetamine (AMPH) (0.2, 2.5, 5.0, 10.0 mg/kg). At the lowest dose tested (0.2 mg/kg), neither D3R mutant mice nor wild-type mice exhibited measurable change in locomotor activity or stereotypy relative to their respective saline-treated controls. D3R mutant mice exhibited a significantly greater increase in locomotor activity, but not stereotypy, relative to wild-type mice in response to treatment with AMPH 2.5 mg/kg. AMPH-induced locomotor activity and stereotypy were similar in both wild-type and D3R mutant mice at both the 5.0 and 10 mg/kg AMPH doses. These findings provide further support for an inhibitory role for the D3R in AMPH-induced locomotor activity, and demonstrate a more limited role for the D3R in modulating AMPH-induced stereotypy.
越来越多的证据表明,多巴胺D3受体(D3R)的刺激通过对抗同时存在的D1R和D2R介导的信号传导,对自发运动和精神兴奋剂诱导的运动具有抑制作用。为了评估该模型,我们使用纯合D3R突变小鼠和野生型对照来研究D3R在急性苯丙胺(AMPH)(0.2、2.5、5.0、10.0 mg/kg)刺激的运动活动和刻板行为中的作用。在测试的最低剂量(0.2 mg/kg)下,与各自的生理盐水处理对照组相比,D3R突变小鼠和野生型小鼠在运动活动或刻板行为方面均未表现出可测量的变化。相对于野生型小鼠,D3R突变小鼠在接受2.5 mg/kg AMPH治疗后,运动活动显著增加,但刻板行为未增加。在5.0和10 mg/kg AMPH剂量下,野生型和D3R突变小鼠的AMPH诱导的运动活动和刻板行为相似。这些发现进一步支持了D3R在AMPH诱导的运动活动中的抑制作用,并证明了D3R在调节AMPH诱导的刻板行为中的作用更为有限。