...
首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >THE PROTECTIVE EFFECTS OF FREE WHEEL-RUNNING AGAINST COCAINE PSYCHOMOTOR SENSITIZATION PERSIST AFTER EXERCISE CESSATION IN C57BL/6J MICE
【24h】

THE PROTECTIVE EFFECTS OF FREE WHEEL-RUNNING AGAINST COCAINE PSYCHOMOTOR SENSITIZATION PERSIST AFTER EXERCISE CESSATION IN C57BL/6J MICE

机译:C57BL / 6J小鼠运动停止后可自由行走对可卡因心理敏化持久性的保护作用

获取原文
获取原文并翻译 | 示例
           

摘要

Previous literature suggests that free access to a running wheel can attenuate the behavioral responsiveness to addictive drugs in rodents. In a few studies, wheel-running cessation accentuated drug responsiveness. Here, we tested whether free wheel-running cessation is followed by (1) an accentuation or (2) an attenuation of cocaine psychomotor sensitization, knowing that no cessation of (continuous) wheel-running is associated with an attenuation of cocaine responsiveness. Male C57BL/6J mice, aged 35 days, were housed singly either with (exercising mice) or without (non-exercising mice) a running wheel. At the end of a period of 36 days, half of the exercising mice were deprived of their wheel whereas the other half of exercising mice kept their wheel until the end of experimentation (which lasted 85 days). The non-exercising mice were housed without wheel throughout experimentation. Testing took place 3 days after exercise cessation. After 2 once-daily drug-free test sessions, mice were tested for initiation of psychomotor sensitization over 13 once-daily injections of 8 mg/kg cocaine. Post-sensitization conditioned activation (saline challenge) and long-term expression of sensitization were assessed 2 or 30 days after the last sensitizing injection (same treatments as for initiation of sensitization), respectively. Exercising mice and mice undergoing wheel-running cessation exhibited comparable degrees of attenuation of all cocaine effects in comparison with the continuously non-exercising mice, which showed the greatest effects. Thus, the efficaciousness of wheel-running at attenuating cocaine sensitization not only resisted to exercise cessation but was also unambiguously persistent (an important effect rarely reported in previous literature). (C) 2015 IBRO. Published by Elsevier Ltd. All rights reserved.
机译:先前的文献表明,自由进入跑轮可以减弱啮齿动物对成瘾性药物的行为反应。在一些研究中,停止转轮加剧了药物的反应性。在这里,我们知道是否停止自由行驶会导致(1)增强或(2)降低可卡因精神运动致敏性,因为知道(持续)行驶不会停止与可卡因反应性降低相关。将35天大的雄性C57BL / 6J小鼠单独饲养(有运动小鼠)或没有(非运动小鼠)跑轮。在36天结束时,一半的运动小鼠被剥夺了轮子,而另一半运动小鼠保持了轮子直到实验结束(持续了85天)。在整个实验过程中,将无运动能力的小鼠不带轮饲养。运动停止后三天进行测试。在每天一次的2次无药测试之后,通过每天13次每天一次的8 mg / kg可卡因注射,对小鼠的精神运动致敏作用进行了测试。在最后一次致敏注射后2天或30天(与致敏作用相同的治疗方法)分别评估致敏后条件性激活(盐水刺激)和致敏作用的长期表达。与持续不运动的小鼠相比,运动的小鼠和进行车轮停止运动的小鼠与所有可卡因作用的衰减程度相当。因此,车轮行驶在减轻可卡因敏化作用方面的功效不仅抗拒运动停止,而且具有持久性(在以前的文献中很少报道这一重要作用)。 (C)2015年IBRO。由Elsevier Ltd.出版。保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号