神经退行性变
痴呆
疾病
神经科学
机制(生物学)
2型糖尿病
胰岛素抵抗
糖尿病
生物信息学
医学
2型糖尿病
高磷酸化
胰岛素
淀粉样蛋白(真菌学)
β淀粉样蛋白
生物
内分泌学
内科学
遗传学
病理
哲学
认识论
激酶
作者
Aparna Chauhan,Sachin Dubey,Smita Jain
摘要
ABSTRACT Diabetes mellitus (DM) and Alzheimer's disease (AD) rates are rising, mirroring the global trend of an aging population. Numerous epidemiological studies have shown that those with Type 2 diabetes (T2DM) have an increased risk of developing dementia. These degenerative and progressive diseases share some risk factors. To a large extent, the amyloid cascade is responsible for AD development. Neurofibrillary tangles induce neurodegeneration and brain atrophy; this chain reaction begins with hyperphosphorylation of tau proteins caused by progressive amyloid beta (Aβ) accumulation. In addition to these processes, it seems that alterations in brain glucose metabolism and insulin signalling lead to cell death and reduced synaptic plasticity in AD, before the onset of symptoms, which may be years away. Due to the substantial evidence linking insulin resistance in the brain with AD, researchers have coined the name “Type 3 diabetes” to characterize the condition. We still know little about the processes involved, even though current animal models have helped illuminate the links between T2DM and AD. This brief overview discusses insulin and IGF‐1 signalling disorders and the primary molecular pathways that may connect them. The presence of GSK‐3β in AD is intriguing. These proteins' association with T2DM and pancreatic β‐cell failure suggests they might be therapeutic targets for both disorders.
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