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介导大脑和认知储备的机制:神经退行性疾病动物模型中的经验依赖性神经保护和功能代偿。

Mechanisms mediating brain and cognitive reserve: experience-dependent neuroprotection and functional compensation in animal models of neurodegenerative diseases.

机构信息

Wellcome Trust Sanger Institute, Cambridge, UK.

出版信息

Prog Neuropsychopharmacol Biol Psychiatry. 2011 Mar 30;35(2):331-9. doi: 10.1016/j.pnpbp.2010.10.026. Epub 2010 Nov 26.

Abstract

'Brain and cognitive reserve' (BCR) refers here to the accumulated neuroprotective reserve and capacity for functional compensation induced by the chronic enhancement of mental and physical activity. BCR is thought to protect against, and compensate for, a range of different neurodegenerative diseases, as well as other neurological and psychiatric disorders. In this review we will discuss BCR, and its potential mechanisms, in neurodegenerative disorders, with a focus on Huntington's disease (HD) and Alzheimer's disease (AD). Epidemiological studies of AD, and other forms of dementia, provided early evidence for BCR. The first evidence for the beneficial effects of enhanced mental and physical activity, and associated mechanistic insights, in an animal model of neurodegenerative disease was provided by experiments using HD transgenic mice. More recently, experiments on animal models of HD, AD and various other brain disorders have suggested potential molecular and cellular mechanisms underpinning BCR. We propose that sophisticated insight into the processes underlying BCR, and identification of key molecules mediating these beneficial effects, will pave the way for therapeutic advances targeting these currently incurable neurodegenerative diseases.

摘要

“大脑与认知储备”(BCR)在此是指通过长期增强脑力和体力活动而积累的神经保护储备和功能代偿能力。BCR 被认为可以预防和代偿一系列不同的神经退行性疾病,以及其他神经和精神疾病。在这篇综述中,我们将讨论神经退行性疾病中的 BCR 及其潜在机制,重点是亨廷顿病(HD)和阿尔茨海默病(AD)。AD 及其他形式痴呆症的流行病学研究为 BCR 提供了早期证据。使用 HD 转基因小鼠的实验首次为神经退行性疾病动物模型中增强的脑力和体力活动及其相关的机制见解提供了有益效果的证据。最近,HD、AD 和各种其他脑疾病动物模型的实验提出了 BCR 潜在的分子和细胞机制。我们提出,对 BCR 背后过程的深入了解,以及确定介导这些有益效果的关键分子,将为针对这些目前无法治愈的神经退行性疾病的治疗进展铺平道路。

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