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阿尔茨海默病中的正反馈环:阿尔茨海默病反馈假说。

Positive Feedback Loops in Alzheimer's Disease: The Alzheimer's Feedback Hypothesis.

机构信息

Division of Neuroscience and Experimental Psychology, School of Biological Sciences, Faculty of Biology Medicine and Health, Oxford Road, University of Manchester, UK.

出版信息

J Alzheimers Dis. 2018;66(1):25-36. doi: 10.3233/JAD-180583.

Abstract

The dominant model for Alzheimer's disease (AD) is the amyloid cascade hypothesis, in which the accumulation of excess amyloid-β (Aβ) leads to inflammation, excess glutamate and intracellular calcium, oxidative stress, tau hyperphosphorylation and tangle formation, neuronal loss, and ultimately dementia. In a cascade, AD proceeds in a unidirectional fashion, with events only affecting downstream processes. Compelling evidence now exists for the presence of positive feedback loops in AD, however, involving oxidative stress, inflammation, glutamate, calcium, and tau. The pathological state of AD is thus a system of positive feedback loops, leading to amplification of the initial perturbation, rather than a linear cascade. Drugs may therefore be effective by targeting numerous points within the loops, rather than concentrating on upstream processes. Anti-inflammatories and anti-oxidants may be especially valuable, since these processes are involved in many loops and hence would affect numerous processes in AD.

摘要

阿尔茨海默病(AD)的主导模型是淀粉样蛋白级联假说,其中过量的淀粉样蛋白-β(Aβ)的积累导致炎症、谷氨酸和细胞内钙过量、氧化应激、tau 过度磷酸化和缠结形成、神经元丧失,最终导致痴呆。在级联中,AD 呈单向进行,事件仅影响下游过程。然而,现在有令人信服的证据表明 AD 中存在正反馈回路,涉及氧化应激、炎症、谷氨酸、钙和 tau。因此,AD 的病理状态是一个正反馈回路系统,导致初始扰动的放大,而不是线性级联。药物可能通过靶向回路中的许多点而不是集中在上游过程而有效。抗炎药和抗氧化剂可能特别有价值,因为这些过程涉及许多回路,因此会影响 AD 中的许多过程。

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