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衰老的大脑。

The aging brain.

作者信息

Yankner Bruce A, Lu Tao, Loerch Patrick

机构信息

Department of Pathology, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Annu Rev Pathol. 2008;3:41-66. doi: 10.1146/annurev.pathmechdis.2.010506.092044.

Abstract

Aging is accompanied by cognitive decline in a major segment of the population and is the primary risk factor for Alzheimer's disease and other prevalent neurodegenerative disorders. Despite this central role in disease pathogenesis and morbidity, the aging of the brain has not been well understood at a molecular level. This review seeks to integrate what is known about age-related cognitive and neuroanatomical changes with recent advances in understanding basic molecular mechanisms that underlie aging. An important issue is how normal brain aging transitions to pathological aging, giving rise to neurodegenerative disorders. Toxic protein aggregates have been identified as potential contributory factors, including amyloid beta-protein in Alzheimer's disease, tau in frontotemporal dementia, and alpha-synuclein in Parkinson's disease. However, current models of pathogenesis do not explain the origin of the common sporadic forms of these diseases or address the critical nexus between aging and disease. This review discusses potential approaches to unifying the systems biology of the aging brain with the pathogenesis of neurodegeneration.

摘要

在大部分人群中,衰老伴随着认知能力下降,并且是阿尔茨海默病和其他常见神经退行性疾病的主要风险因素。尽管衰老在疾病发病机制和发病率中起着核心作用,但在分子水平上,人们对大脑衰老的了解还不够深入。本综述旨在将已知的与年龄相关的认知和神经解剖学变化与理解衰老基础的基本分子机制的最新进展相结合。一个重要问题是正常脑衰老如何转变为病理性衰老,进而引发神经退行性疾病。有毒蛋白质聚集体已被确定为潜在的促成因素,包括阿尔茨海默病中的淀粉样β蛋白、额颞叶痴呆中的tau蛋白以及帕金森病中的α-突触核蛋白。然而,目前的发病机制模型无法解释这些疾病常见散发性形式的起源,也未涉及衰老与疾病之间的关键联系。本综述讨论了将衰老大脑的系统生物学与神经退行性变发病机制统一起来的潜在方法。

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