Diabetes mellitus and Alzheimer's disease: GSK-3β as a potential link

作者：Zhang, Ying; Huang, Nan-qu; Yan, Fei; Jin, Hai; Zhou, Shao-yu; Shi, Jing-shan; Jin, Feng^*

来源：Behavioural Brain Research, 2018, 339: 57-65.

DOI：10.1016/j.bbr.2017.11.015

• Glycogen synthase kinase-3 beta
• Diabetes mellitus
• Alzheimer's disease
• Microtubule-associated protein tau
• Insulin resistance

It is well known that Alzheimer's disease (AD) is closely related to diabetes mellitus (DM), and AD is also regarded as Type 3 diabetes (T3D). However, the exact link between AD and DM is still unclear. Recently, more and more evidence has shown that glycogen synthase kinase-3 beta (GSK-3 beta) may be the potential link between DM and AD. In DM, GSK-3 beta is the crucial enzyme of glycogen synthesis, which plays a key role in regulating blood glucose. More importantly, GSK-3 beta is one of the key factors leading to insulin deficiency and insulin resistance, and insulin resistance is an import ant hallmark of the occurrence and development of DM. In AD, GSK-3 beta plays an important role in hyperphosphorylation of microtubule-associated protein tau (tau), which is one of the pathological features in AD. GSK-3 beta is one of the important kinases of tau phosphorylation and is involved in the insulin/phosphoinositide 3-kinase/protein kinase B (insulin/PI3K/Akt) signaling pathway. Dysfunction of the insulin/PI3K/Akt signaling pathway, which regulates glucose metabolism in the brain, can lead to tau hyperphosphorylation in the brain of AD patents. Additionally, insulin resistance in DM may cause beta-amyloid (AD) deposition, which will be cleared by tau, but excessive phosphorylation of tau will further aggravate the neurotoxicity; then damage the brain and affect the cognitive function. GSK-3 beta is considered as a common kinase in insulin signaling transduction and tau protein phosphorylation, so we have reasons to believe that GSK-3 beta is a potential link between DM and AD.

• 出版日期2018-2-26
• 单位遵义医科大学