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

Akhisaroglu M., KÜRTÜNCÜ M., Manev H., Uz T.

PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, vol.80, no.3, pp.371-377, 2005 (SCI-Expanded) identifier

  • Publication Type: Article / Article
  • Volume: 80 Issue: 3
  • Publication Date: 2005
  • Doi Number: 10.1016/j.pbb.2004.11.016
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.371-377
  • Keywords: behavioral sensitization, tolerance, striatum, dopamine receptor rhythm, circadian, inbred mice, COCAINE SENSITIZATION, DOPAMINE-RECEPTOR, CIRCADIAN-RHYTHMS, MELATONIN RECEPTORS, NUCLEUS-ACCUMBENS, DEFICIENT MICE, RAT, TOLERANCE, D2, MODULATION
  • Istanbul University Affiliated: No


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. (c) 2004 Elsevier Inc. All rights reserved.