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从肥胖症到阿尔茨海默病,皆与胰岛素抵抗有关。

From obesity to Alzheimer's disease through insulin resistance.

作者信息

Terzo Simona, Amato Antonella, Mulè Flavia

机构信息

Dipartimento di Scienze e Tecnologie Biologiche Chimiche e Farmaceutiche (STEBICEF), Università di Palermo, 90128, Italy.

出版信息

J Diabetes Complications. 2021 Nov;35(11):108026. doi: 10.1016/j.jdiacomp.2021.108026. Epub 2021 Aug 18.

Abstract

Alzheimer's disease is one of the most frequent forms of dementia. It is a progressive neurodegenerative disease, characterized by presence of amyloid plaques and neurofibrillary tangles in the brain. Obesity is regarded as abnormal fat accumulation with deleterious impact on human health. There is full scientific evidence that obesity and the metabolic comorbidities (e.g., insulin resistance, hyperglycaemia, and type 2 diabetes) are related to Alzheimer's disease and likely in the causative pathway. Numerous studies have identified several overlapping neurodegenerative mechanisms, including oxidative stress, mitochondrial dysfunction, and inflammation. In this review, we present how obesity and the associated lipotoxicity as well as chronic inflammation initiate a state of insulin resistance that in turn, may have a role in causing the characteristic cerebral alterations of AD. In particular, we focus on the molecular mechanisms linking the obesity-induced impairment in insulin signalling to the upregulation of Aβ aggregation, tau hyper-phosphorylation, inflammation, oxidative stress and mitochondrial dysfunction.

摘要

阿尔茨海默病是最常见的痴呆形式之一。它是一种进行性神经退行性疾病,其特征是大脑中存在淀粉样斑块和神经原纤维缠结。肥胖被视为异常脂肪堆积,对人类健康有有害影响。有充分的科学证据表明,肥胖和代谢合并症(如胰岛素抵抗、高血糖和2型糖尿病)与阿尔茨海默病相关,且可能处于致病途径中。众多研究已经确定了几种重叠的神经退行性机制,包括氧化应激、线粒体功能障碍和炎症。在本综述中,我们阐述了肥胖及相关的脂毒性以及慢性炎症如何引发胰岛素抵抗状态,而胰岛素抵抗反过来可能在导致AD的典型脑改变中起作用。特别是,我们关注将肥胖诱导的胰岛素信号传导受损与Aβ聚集上调、tau过度磷酸化、炎症、氧化应激和线粒体功能障碍联系起来的分子机制。

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