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左旋多巴诱导的帕金森病神经退行性变的解毒和抗氧化治疗。

Detoxification and antioxidative therapy for levodopa-induced neurodegeneration in Parkinson's disease.

机构信息

Department of Neurology, St. Joseph Hospital Berlin-Weißensee, Gartenstr. 1, 13088, Berlin, Germany.

出版信息

Expert Rev Neurother. 2013 Jun;13(6):707-18. doi: 10.1586/ern.13.50.

Abstract

Levodopa is the most efficacious drug treatment option for Parkinson's disease. However, in particular, high levodopa dosing may contribute to disease progression. Chronic levodopa metabolism reduces the methylation capacity and the antioxidant defense. Thus, this levodopa-induced free radical production complements the disease process, which considerably depends on free radical-induced, apoptotic neuronal cell death. Accordingly, clinical long-term studies with in the laboratory neuroprotective compounds failed in clinical investigations, as these studies were performed in levodopa-naive patients with Parkinson's disease over a relative short interval. Therefore, the likelihood for a positive outcome was rather low, since trials only focused on the disease process in levodopa-naive patients. However, studies on antioxidant therapeutic strategies were positive in levodopa-treated Parkinson's disease patients. To counteract these metabolic long-term levodopa-associated effects, chronic levodopa therapy should be combined with supplemental application of free radical scavengers and methyl group donating vitamins.

摘要

左旋多巴是治疗帕金森病最有效的药物选择。然而,特别是高剂量的左旋多巴可能会导致疾病进展。慢性左旋多巴代谢会降低甲基化能力和抗氧化防御能力。因此,这种由左旋多巴引起的自由基产生补充了疾病过程,这在很大程度上取决于自由基诱导的、凋亡性神经元细胞死亡。因此,在实验室神经保护化合物的临床长期研究在临床研究中失败,因为这些研究是在帕金森病的左旋多巴未治疗患者中进行的,时间相对较短。因此,阳性结果的可能性相当低,因为试验仅集中在左旋多巴未治疗患者的疾病过程上。然而,抗氧化治疗策略的研究在接受左旋多巴治疗的帕金森病患者中是阳性的。为了抵消这些与长期使用左旋多巴相关的代谢影响,慢性左旋多巴治疗应该与自由基清除剂和提供甲基的维生素的补充应用相结合。

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