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Modulation of pro-inflammatory response in a mouse model of Parkinson's disease by non-invasive physical approach

机译:通过非侵入性物理方法对帕金森氏病小鼠模型中促炎反应的调节

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The aim of this study is to investigate the effect of a non-invasive physical treatment on activated microglia of a well-established mouse model of Parkinson disease (PD), based on intoxication with 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP). To this aim, we proposed a Radio electric asymmetric conveyer (REAC) technology, with its specific therapeutic protocols of regenerative medicine: tissue optimization - regenerative (TO-RGN), as an innovative therapeutic strategy for the treatment of PD. We observed that REAC TO-RGN exposition can attenuate the damage of nigrostriatal pathway induced by MPTP treatment in mice, decreasing levels of pro-inflammatory mediators in the substantia nigra pars compacta (SNpc) of MPTP-mice. Besides, TH immunostaining in MPTP-treated mice exposed to REAC TO-RGN resulted more pronounced in both substantia nigra and striatum in comparison to animals that received only MPTP treatment. Overall, these data suggest that REAC TO-RGN treatment can have neuroprotective effects in MPTP-induced PD mice model, which may be related to reduced inflammatory reaction.
机译:这项研究的目的是基于1-甲基-4-苯基-1,2的中毒作用,研究无创物理治疗对成熟的帕金森病(PD)小鼠模型的活化小胶质细胞的影响, 3,6-四氢吡啶(MPTP)。为此,我们提出了一种无线电不对称传送带(REAC)技术,其具有再生医学的特定治疗方案:组织优化-再生(TO-RGN),作为治疗PD的创新治疗策略。我们观察到REAC TO-RGN暴露可以减轻小鼠MPTP处理诱导的黑质纹状体途径的损害,降低MPTP小鼠黑质致密部(SNpc)中促炎性介质的水平。此外,与仅接受MPTP处理的动物相比,暴露于REAC TO-RGN的MPTP处理的小鼠的TH免疫染色在黑质和纹状体中均表现得更为明显。总体而言,这些数据表明REAC TO-RGN治疗在MPTP诱导的PD小鼠模型中可能具有神经保护作用,这可能与炎症反应减少有关。

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