胰岛素抵抗
2型糖尿病
2型糖尿病
疾病
碳水化合物代谢
糖尿病
医学
阿尔茨海默病
胰岛素降解酶
老化
病态的
内分泌学
神经科学
葡萄糖摄取
酶
生物信息学
内科学
胰岛素
生物
生物化学
作者
Ai Sze Wee,Thao Dinh Nhu,Kooi Yeong Khaw,Kim San Tang,Keng Yoon Yeong
标识
DOI:10.2174/1570159x21999221111102343
摘要
Alzheimer's disease (AD) and type 2 diabetes mellitus (DM) are more prevalent with ageing and cause a substantial global socio-economic burden. The biology of these two conditions is well elaborated, but whether AD and type 2 DM arise from coincidental roots in ageing or are linked by pathophysiological mechanisms remains unclear. Research findings involving animal models have identified mechanisms shared by both AD and type 2 DM. Deposition of β-amyloid peptides and formation of intracellular neurofibrillary tangles are pathological hallmarks of AD. Type 2 DM, on the other hand, is a metabolic disorder characterised by hyperglycaemia and insulin resistance. Several studies show that improving type 2 DM can delay or prevent the development of AD, and hence, prevention and control of type 2 DM may reduce the risk of AD later in life. Alpha-glucosidase is an enzyme that is commonly associated with hyperglycaemia in type 2 DM. However, it is uncertain if this enzyme may play a role in the progression of AD. This review explores the experimental evidence that depicts the relationship between dysregulation of glucose metabolism and AD. We also delineate the links between alpha-glucosidase and AD and the potential role of alpha-glucosidase inhibitors in treating AD.
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