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On the pathogenesis and neuroprotective treatment of Parkinson disease: what have we learned from the genetic forms of this disease?

机译:关于帕金森病的发病机理和神经保护性治疗:我们从帕金森病的遗传形式中学到了什么?

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摘要

Parkinson's disease (PD) is a neurodegenerative disorder affecting nearly 3 million patients in Europe and North America, characterized by a core phenotype of motor deficits, akinesia, rigidity, postural disturbance and tremor, which is complicated by other neurological deficits during its long progression. Our knowledge about the pathophisiology of PD was limited, up to 25 years ago, to the observation of the lesion of the nigro-striatal dopamine neurons in these patients. The subjects who developed PD as a consequence of exposure to neurotoxic compounds, increased our knowledge about the pathogenesis of this disease. More recently, genetic alterations have been found in patients with PD. The function of the proteins coded by the genes involved in PD has been investigated in genetic models of this disease from invertebrate to rodents. Mutated proteins responsible for PD have been tested in vivo and in vitro, in cellular models or in artificial constructs. A wealth of important information about the function of alpha-synuclein, parkin, DJ-1, PINK and dardarin is available, most notably about the first two causes of familial PD discovered, alpha-synuclein and parkin, responsible for autosomal dominant and autosomal recessive PD, respectively. Different animal models of alpha-synuclein and parkin have been extensively investigated. The in vitro and in vivo studies performed in genetic models of PD have shown that the proteins involved in the pathogenesis of PD interact with one another and have multiple mechanisms of cell toxicity. From the available data, it is clear that the mechanisms leading to cell degeneration in PD are variable in the different subtypes of this disease. Neuroprotective therapies should, therefore, be multiple and tailored according to the factors involved in the different cases. In this study, we review what we have learned from the genetic models of PD and the putative strategies to be tested in the near future.
机译:帕金森氏病(PD)是一种神经退行性疾病,在欧洲和北美地区影响了近300万患者,其特征是运动功能障碍,运动障碍,僵硬,体位障碍和震颤的核心表型,在其长期发展过程中还伴有其他神经功能障碍。直到25年前,我们对PD病理学的了解仅限于观察这些患者的黑质纹状体多巴胺神经元病变。由于暴露于神经毒性化合物而导致PD的受试者增加了我们对该病发病机理的了解。最近,在PD患者中发现了遗传改变。从无脊椎动物到啮齿动物的这种疾病的遗传模型已经研究了PD相关基因编码的蛋白质的功能。负责PD的突变蛋白已在体内和体外,细胞模型或人工构建物中进行了测试。关于α-突触核蛋白,parkin,DJ-1,PINK和dardarin的功能,有大量重要信息可供使用,最值得注意的是有关发现的家族性PD的前两个原因,α-突触核蛋白和parkin导致常染色体显性遗传和常染色体隐性遗传PD,分别。已经广泛研究了α-突触核蛋白和帕金森氏病的不同动物模型。在PD的遗传模型中进行的体外和体内研究表明,参与PD发病机理的蛋白质彼此相互作用,并具有多种细胞毒性机制。从现有数据来看,很明显,导致PD细胞变性的机制在该疾病的不同亚型中是可变的。因此,神经保护疗法应该是多种多样的,并应根据不同情况下涉及的因素进行调整。在这项研究中,我们回顾了从PD的遗传模型中学到的知识以及在不久的将来要测试的推定策略。

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