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Neuroplasticity and Neuroprotective Effect of Treadmill Training in the Chronic Mouse Model of Parkinsons Disease

机译:跑步机训练对帕金森氏病慢性小鼠模型的神经可塑性和神经保护作用

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摘要

Physical training confers protection to dopaminergic neurons in rodent models of parkinsonism produced by neurotoxins. The sparing effect of physical training on dopaminergic neurons can be tested with training applied during chronic MPTP treatment, while the neurorestorative effect when training is applied after completing such treatment. In this study, the effect of the onset of training respective to chronic MPTP treatment was specifically addressed. Three groups of mice were injected with 10 doses of MPTP (12.5 mg/kg/injection) over 5 weeks. The first group remained sedentary; the second one underwent early onset training, which started 1 week before commencing MPTP treatment, continued throughout 5 weeks of treatment and 4 weeks thereafter; the third group underwent late-onset training of the same length and intensity as the former group, except that it started immediately after the end of MPTP treatment. Two groups served as controls: a saline-injected group that remained sedentary and saline-injected group, which underwent the same training as the early and late-onset training groups. Both early and late-onset physical training saved almost all nigral and VTA dopaminergic neurons, prevented inflammatory response, and increased the BDNF and GDNF levels to a similar extent. From these results one may conclude that early and late-onset training schedules were equipotent in their neuroprotective effect and that the mechanism of neuroprotection was similar. The sparing effect of early onset training may be satisfactorily explained by assuming that the increased level of BDNF and GDNF prevented the degeneration of dopaminergic neurons. To explain a similar number of dopaminergic neurons detected at the end of the early and late-onset training, one should additionally assume that the former training schedule induced neurogenesis. Results of this study support the view that physical activity may be neuroprotective even at a more advanced stage of PD and justify starting physical activity at any point of the disease.
机译:在神经毒素产生的帕金森氏病的啮齿动物模型中,体育锻炼可以保护多巴胺能神经元。可以通过在慢性MPTP治疗期间进行的训练来检验体育锻炼对多巴胺能神经元的保留作用,而在完成这种治疗后进行训练时可以起到神经修复作用。在这项研究中,专门针对慢性MPTP治疗开始训练的效果。三组小鼠在5周内注射了10剂MPTP(12.5毫克/千克/注射)。第一组久坐不动;第二次接受早期发作训练,该训练在开始MPTP治疗前1周开始,在整个治疗5周和此后4周持续进行;第三组接受了与前一组相同的长度和强度的后期发作训练,只是它在MPTP治疗结束后立即开始。两组作为对照组:静坐的注射盐水组和注射盐水的组,它们接受了与早期和晚期发作组相同的训练。早期和晚期发作的体育锻炼都几乎挽救了所有的黑色和VTA多巴胺能神经元,防止了炎症反应,并以类似的程度增加了BDNF和GDNF的水平。从这些结果可以得出结论,早期和晚期发作的训练计划在神经保护作用上是等效的,并且神经保护的机制是相似的。可以通过假设BDNF和GDNF的水平升高阻止多巴胺能神经元的退化来令人满意地解释早期发作训练的微不足道的作用。为了解释在早期和晚期发作训练结束时检测到的类似数量的多巴胺能神经元,应该另外假设以前的训练计划会诱导神经发生。这项研究的结果支持这样一种观点,即即使在PD的较晚期阶段,体育锻炼也可能具有神经保护作用,并证明在疾病的任何部位开始体育锻炼都是合理的。

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