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Promising Effects of Neurorestorative Diets on Motor, Cognitive, and Gastrointestinal Dysfunction after Symptom Development in a Mouse Model of Parkinson's Disease

机译:神经恢复饮食对帕金森氏病小鼠模型中症状发展后运动,认知和胃肠功能障碍的有前途的影响

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Parkinson's disease (PD) is characterized by the progressive degeneration of dopaminergic nigrostriatal neurons, with reductions in the function and amount of dopaminergic synapses. Therefore, synapse loss and membrane-related pathology provide relevant targets for interventions in PD. We previously showed the beneficial preventive effects of a dietary intervention containing uridine and DHA, two precursors for membrane synthesis, in the intrastriatal rotenone model for PD. Here, we examined the therapeutic potential of the same dietary intervention on motor, cognitive, and gastrointestinal symptoms. In addition, we tested the effects of an extended nutritional formula based on the same precursors plus other nutrients that increase membrane phospholipid synthesis as well as prebiotic fibers. C57BL/6J mice received a unilateral rotenone injection in the striatum. Dietary interventions started 28 days after surgery, when motor-symptoms had developed. Readout parameters included behavioral tasks measuring motor function and spatial memory as well as intestinal function and histological examination of brain and gut to assess PD-like pathology. Our results show that rotenone-induced motor and non-motor problems were partially alleviated by the therapeutic dietary interventions providing uridine and DHA. The extended nutritional intervention containing both precursors and other nutrients that increase phospholipid synthesis as well as prebiotic fibers was more effective in normalizing rotenone-induced motor and non-motor abnormalities. The latter diet also restored striatal DAT levels, indicating its neurorestorative properties. This is the first study demonstrating beneficial effects of specific dietary interventions, given after full development of symptoms, on a broad spectrum of motor and non-motor symptoms in a mouse model for PD.
机译:帕金森氏病(PD)的特征是多巴胺能黑质纹状体神经元逐渐退化,多巴胺能突触的功能和数量减少。因此,突触丢失和膜相关病理提供了针对PD干预的相关目标。我们之前在PD的纹状体鱼藤酮模型中显示了含有尿苷和DHA(两种用于膜合成的前体)的饮食干预的有益预防作用。在这里,我们检查了相同饮食干预对运动,认知和胃肠道症状的治疗潜力。此外,我们基于相同的前体以及其他增加膜磷脂合成和益生元纤维的营养素,测试了扩展营养配方的效果。 C57BL / 6J小鼠在纹状体中接受了单侧鱼藤酮注射。运动症状出现后,在手术后28天开始进行饮食干预。读出的参数包括测量运动功能和空间记忆以及肠道功能的行为任务,以及脑和肠道的组织学检查,以评估PD样病理。我们的结果表明,通过提供尿苷和DHA的治疗性饮食干预可部分缓解鱼藤酮引起的运动和非运动问题。扩展的营养干预措施既包含增加磷脂合成的前体和其他营养素,又包含益生元纤维,在规范鱼藤酮诱导的运动和非运动异常方面更有效。后者的饮食也恢复了纹状体的DAT水平,表明其神经修复特性。这是第一个证明特定饮食干预措施在症状完全发展后给予PD小鼠模型中广泛的运动和非运动症状的有益影响的第一项研究。

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