Rauhut Anthony S, Warnick Justina A
Psychology Department, Dickinson College, Carlisle, PA 17013, United States; Neuroscience Program, Dickinson College, Carlisle, PA 17013, United States.
Neuroscience Program, Dickinson College, Carlisle, PA 17013, United States.
Neuroscience. 2020 Aug 21;442:114-123. doi: 10.1016/j.neuroscience.2020.07.001. Epub 2020 Jul 9.
The timing of voluntary exercise relative to drug conditioning is important to its "neuroprotective" effects, though it is unclear whether the voluntary exercise needs to occur temporally contiguous with drug conditioning, or occur during an early, developmental period, but non-contiguous with drug conditioning, for its "neuroprotective" effects. To distinguish between these two ideas, the timing of voluntary exercise relative to drug conditioning on the development and extinction of conditioned hyperactivity, and induction of sensitization was manipulated in the present experiment. Specifically, half of the exercise mice were permitted access to home-cage running wheels for 6 continuous weeks (Exercise-Exercise) whereas the other half of the exercise mice were permitted access to home-cage running wheels only for the first 3 weeks and then had the wheels removed (Exercise-Sedentary). Likewise, half of the sedentary mice had no home-cage running wheels for 6 continuous weeks (Sedentary-Sedentary) whereas the other half of the sedentary mice were permitted access to the home-cage running wheels for the last 3 weeks prior to the acquisition phase (Sedentary-Exercise). Mice received vehicle or methamphetamine (Meth; 1.0 mg/kg; acquisition), followed by saline-alone sessions (extinction) and finally challenged with an escalating Meth-regimen (0.25 → 1.0 mg/kg). While all Meth-paired groups, regardless of exercise regimen, showed conditioned hyperactivity, Exercise-Exercise and Exercise-Sedentary mice were less responsive to chronic Meth exposure and showed slower extinction compared to the other Meth-paired groups. These results suggest an early exercise regimen, during a critical developmental window, protects against the stimulant properties of Meth and simultaneously facilitates contextual learning.
自愿运动相对于药物条件作用的时间安排对其“神经保护”作用很重要,不过目前尚不清楚自愿运动是需要与药物条件作用在时间上连续发生,还是在早期发育阶段发生但与药物条件作用不连续,才能产生其“神经保护”作用。为了区分这两种观点,在本实验中对自愿运动相对于药物条件作用在条件性多动的发展和消退以及敏化诱导方面的时间安排进行了操控。具体而言,一半的运动小鼠被允许连续6周使用笼内跑步轮(运动-运动组),而另一半运动小鼠仅在前3周被允许使用笼内跑步轮,然后将跑步轮移除(运动-静止组)。同样,一半的静止小鼠连续6周没有笼内跑步轮(静止-静止组),而另一半静止小鼠在获得阶段前的最后3周被允许使用笼内跑步轮(静止-运动组)。小鼠接受溶剂或甲基苯丙胺(甲基苯丙胺;1.0毫克/千克;获得阶段),随后进行仅注射生理盐水的实验(消退阶段),最后用递增的甲基苯丙胺方案(0.25→1.0毫克/千克)进行挑战。虽然所有与甲基苯丙胺配对的组,无论运动方案如何,都表现出条件性多动,但与其他与甲基苯丙胺配对的组相比,运动-运动组和运动-静止组小鼠对慢性甲基苯丙胺暴露的反应较小,且消退较慢。这些结果表明,在关键发育窗口期间的早期运动方案可预防甲基苯丙胺的刺激特性,并同时促进情境学习。