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喹吡罗诱导的小鼠运动行为及纹状体D2/D3受体水平的昼夜节律

Diurnal rhythms in quinpirole-induced locomotor behaviors and striatal D2/D3 receptor levels in mice.

作者信息

Akhisaroglu Mustafa, Kurtuncu Murat, Manev Hari, Uz Tolga

机构信息

Psychiatric Institute, Department of Psychiatry, University of Illinois at Chicago, 1601 West Taylor Street, M/C 912, Chicago, Illinois 60612, USA.

出版信息

Pharmacol Biochem Behav. 2005 Mar;80(3):371-7. doi: 10.1016/j.pbb.2004.11.016. Epub 2005 Jan 28.

DOI:10.1016/j.pbb.2004.11.016
PMID:15740778
Abstract

Dopaminergic drugs, including the D2/D3 agonist quinpirole, produce lasting changes in the brain that lead to altered behavioral responses. The action of these drugs is dosing time-dependent; in fruit flies, behavioral response to quinpirole shows a marked circadian variability. Here we demonstrate diurnal rhythm-dependent variations both in quinpirole-induced locomotor behaviors and in striatal D2 and D3 protein levels in mice. We found opposing diurnal rhythms in striatal D2 and D3 protein levels, resulting in a high D2/D3 ratio during the day and a low D2/D3 ratio at night. Protracted quinpirole treatment differentially altered striatal D2/D3 rhythms depending on the time of injection (i.e., day or night). When quinpirole-induced locomotor activity was analyzed for 90 min, we found hypomotility after the first day or nighttime drug injection. By the seventh injection, daytime quinpirole treatment produced clear hyperactivity while nighttime quinpirole treatment continued to induce a significant initial hypoactivity followed by a hyperactivity period. Our data indicate that quinpirole-induced long-term alterations in the brain include dosing time-dependent changes in dopamine receptor rhythms. Therefore, we propose that diurnal mechanisms, which participate in drug-induced long-term changes in the dopamine system, are important for the development of dopaminergic behaviors.

摘要

多巴胺能药物,包括D2/D3激动剂喹吡罗,会在大脑中产生持久变化,进而导致行为反应改变。这些药物的作用具有给药时间依赖性;在果蝇中,对喹吡罗的行为反应表现出明显的昼夜节律变化。在此,我们证明了喹吡罗诱导的小鼠运动行为以及纹状体D2和D3蛋白水平存在昼夜节律依赖性变化。我们发现纹状体D2和D3蛋白水平呈现相反的昼夜节律,导致白天D2/D3比例高,夜间D2/D3比例低。长期喹吡罗治疗根据注射时间(即白天或晚上)对纹状体D2/D3节律产生不同影响。当对喹吡罗诱导的运动活动进行90分钟分析时,我们发现在第一天或夜间注射药物后出现运动迟缓。到第七次注射时,白天给予喹吡罗治疗会产生明显的多动,而夜间给予喹吡罗治疗则继续诱导显著的初始运动不足,随后是多动期。我们的数据表明,喹吡罗诱导的大脑长期变化包括多巴胺受体节律的给药时间依赖性变化。因此,我们提出参与多巴胺系统药物诱导长期变化的昼夜机制对多巴胺能行为的发展很重要。

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