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[神经退行性疾病的病理学:特别提及帕金森病和肌萎缩侧索硬化症]

[Pathology of neurodegenerative diseases: with special reference to Parkinson's disease and amyotrophic lateral sclerosis].

作者信息

Takahashi Hitoshi

机构信息

Department of Pathology, Brain Research Institute, Niigata University.

出版信息

Rinsho Shinkeigaku. 2002 Nov;42(11):1085-7.

Abstract

The causes of Parkinson's disease (PD) and amyotrophic lateral sclerosis (ALS) are still unknown. Aging, environmental factors and genetic factors may be involved in the development of these illnesses, especially the sporadic phenotypes. The details of PD pathology have made remarkable advances in the last 5 years, after the discovery of mutation of the alpha-synuclein gene in families with PD: all of the Lewy bodies (Lewy filaments) in familial and sporadic PD contain the gene product alpha-synuclein. Further studies are necessary to elucidate the mechanisms underlying the development of PD, and to determine the therapeutic targets through which it may be possible to prevent the disease. With regard to the pathology of ALS, it is of great importance that in this disease, characteristic neuronal cytoplasmic inclusions (i.e., Bunina bodies and ubiquitinated inclusions) have been described in the lower motor neurons. At present, however, compared with the Lewy bodies in PD, much less is known about the profiles of the inclusions associated with ALS. Early identifications of the proteins that constitute these inclusions would be desirable if we are to elucidate the molecular pathology, and thus the mechanisms underlying ALS.

摘要

帕金森病(PD)和肌萎缩侧索硬化症(ALS)的病因仍不明确。衰老、环境因素和遗传因素可能与这些疾病的发生有关,尤其是散发性病例。在发现帕金森病家族中α-突触核蛋白基因突变后,过去5年帕金森病病理学细节取得了显著进展:家族性和散发性帕金森病中的所有路易小体(路易细丝)均含有基因产物α-突触核蛋白。有必要进一步开展研究以阐明帕金森病的发病机制,并确定可能预防该病的治疗靶点。关于肌萎缩侧索硬化症的病理学,重要的是在这种疾病中,已在脊髓前角运动神经元中描述了特征性的神经元胞质内含物(即布尼亚小体和泛素化内含物)。然而目前,与帕金森病中的路易小体相比,人们对肌萎缩侧索硬化症相关内含物的情况了解要少得多。如果我们要阐明分子病理学,进而了解肌萎缩侧索硬化症的发病机制,那么尽早鉴定构成这些内含物的蛋白质将是可取的。

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