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脑老化:健康与神经退行性变之间的两面神。

Brain aging: A Ianus-faced player between health and neurodegeneration.

机构信息

Laboratory of Prion Biology, Department of Neuroscience, Scuola Internazionale Superiore di Studi Avanzati, Trieste, Italy.

出版信息

J Neurosci Res. 2020 Feb;98(2):299-311. doi: 10.1002/jnr.24379. Epub 2019 Jan 11.

Abstract

Neurodegenerative diseases are incurable debilitating disorders characterized by structural and functional neuronal loss. Approximately 30 million people are affected worldwide, and this number is predicted to reach more than 150 million by 2050. Neurodegenerative disorders include Alzheimer's, Parkinson's, and prion diseases among others. These disorders are characterized by the accumulation of aggregating proteins forming amyloid, responsible for the disease-associated pathological lesions. The aggregation of amyloidogenic proteins can result either in gaining of toxic functions, derived from the damage provoked by these deposits in affected tissue, or in a loss of functions, due to the sequestration and the consequent inability of the aggregating protein to ensure its physiological role. While it is widely accepted that aging represents the main risk factor for neurodegeneration, there is still no clear cut-off line between the two conditions. Indeed, many of the pathways that are commonly altered in neurodegeneration-misfolded protein accumulation, chronic inflammation, mitochondrial dysfunction, impaired iron homeostasis, epigenetic modifications-have been often correlated also with healthy aging. This overlap could be explained by the fact that the continuous accumulation of cellular damages, together with a progressive decline in metabolic efficiency during aging, makes the neurons more vulnerable to toxic injuries. When a given threshold is exceeded, all these alterations might give rise to pathological phenotypes that ultimately lead to neurodegeneration.

摘要

神经退行性疾病是一种无法治愈的使人虚弱的疾病,其特征是结构和功能神经元的丧失。全球约有 3000 万人受到影响,预计到 2050 年,这一数字将超过 1.5 亿。神经退行性疾病包括阿尔茨海默病、帕金森病和朊病毒病等。这些疾病的特征是聚集蛋白的积累形成淀粉样蛋白,这是导致与疾病相关的病理损伤的原因。淀粉样蛋白形成蛋白的聚集既可以获得毒性功能,这是由这些沉积物在受影响的组织中引起的损伤引起的,也可以丧失功能,这是由于聚集蛋白的隔离和随之而来的无法确保其生理功能。虽然普遍认为衰老代表神经退行性变的主要危险因素,但两者之间并没有明确的界限。事实上,在神经退行性变中经常改变的许多途径-错误折叠蛋白的积累、慢性炎症、线粒体功能障碍、铁稳态失调、表观遗传修饰-也常常与健康衰老相关。这种重叠可以用以下事实来解释:细胞损伤的持续积累,以及衰老过程中代谢效率的逐渐下降,使神经元更容易受到毒性损伤。当达到某个阈值时,所有这些改变都可能导致最终导致神经退行性变的病理表型。

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