Geuzaine Annabelle, Tirelli Ezio
Université de Liège, Belgium.
Université de Liège, Belgium.
Behav Brain Res. 2014 Apr 1;262:57-67. doi: 10.1016/j.bbr.2014.01.002. Epub 2014 Jan 13.
Previous literature suggests that physical exercise allowed by an unlimited access to a running wheel for several weeks can mitigate chronic neurobehavioral responsiveness to several addictive drugs in rodents. Here, the potential preventive effects of unlimited wheel-running on the initiation of psychomotor sensitization and the acquisition and extinction of conditioned place preference (CPP) induced by 10 mg/kg cocaine in C56BL/6J mice were assessed in two independent experiments. To this end, half of the mice were singly housed with a running wheel at 28 days of age for 10 weeks prior to psychopharmacological tests, during which housing conditions did not change, and the other half of mice were housed without running wheel. In Experiment 1, prior to initiating sensitization, psychomotor activity on the two first drug-free once-daily sessions was not affected by wheel-running. This was also found for the acute psychomotor-activating effect of cocaine on the first sensitization session. Psychomotor sensitization readily developed over the 9 following once-daily sessions in mice housed without wheel, whereas it was inhibited in mice housed with a wheel. However, that difference did not transfer to post-sensitization conditioned activity. In contrast with the sensitization results, mice housed with a wheel still expressed a clear-cut CPP which did not extinguish differently from that of the other group, a result in disaccord with previous studies reporting either an attenuating or an increasing effect of wheel-running on cocaine-induced conditioned reward. The available results together indicate that interactions between wheel-running and cocaine effects are far from being satisfactorily characterized.
先前的文献表明,让啮齿动物在数周内无限制地使用跑步轮进行体育锻炼,可以减轻其对几种成瘾药物的慢性神经行为反应。在此,在两项独立实验中评估了无限制跑步对C57BL/6J小鼠中由10mg/kg可卡因诱导的精神运动敏化的起始以及条件性位置偏爱(CPP)的获得和消退的潜在预防作用。为此,在进行精神药理学测试前,一半小鼠在28日龄时单独饲养并配备跑步轮,持续10周,在此期间饲养条件不变,另一半小鼠则饲养在没有跑步轮的环境中。在实验1中,在开始敏化之前,最初两次无药物的每日一次实验中的精神运动活动不受跑步轮的影响。在第一次敏化实验中,可卡因的急性精神运动激活作用也有同样的结果。在没有跑步轮饲养的小鼠中,精神运动敏化在随后的9次每日一次实验中很容易发展,而在有跑步轮饲养的小鼠中则受到抑制。然而,这种差异并未转移到敏化后的条件性活动中。与敏化结果相反,有跑步轮饲养的小鼠仍然表现出明显的CPP,其消退情况与另一组没有差异,这一结果与先前报道跑步轮对可卡因诱导的条件性奖赏有减弱或增强作用的研究不一致。现有结果共同表明,跑步轮与可卡因作用之间的相互作用远未得到令人满意的表征。