Shared signaling pathways in Alzheimer's and metabolic disease may point to new treatment approaches

被引:18
|
作者
Suresh, Jahnavi [1 ]
Khor, Ing Wei [2 ]
Kaur, Prameet [1 ]
Heng, Hui Li [3 ,4 ,5 ]
Torta, Federico [6 ]
Dawe, Gavin S. [3 ,4 ,5 ]
Tai, E. Shyong [2 ,7 ]
Tolwinski, Nicholas S. [1 ]
机构
[1] Yale NUS Coll, Sci Div, Singapore, Singapore
[2] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Med, Singapore, Singapore
[3] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Pharmacol, Singapore, Singapore
[4] Neurobiol Programme, Singapore, Singapore
[5] Natl Univ Singapore, Life Sci Inst, Singapore, Singapore
[6] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Biochem, Singapore Lipid Incubator, Singapore, Singapore
[7] Natl Univ Hlth Syst, Natl Univ Hosp, Div Endocrinol, Singapore, Singapore
关键词
Alzheimer's disease; amyloid-beta; lipids; metabolic disease; optogenetics; signal transduction; type 2 diabetes mellitus; BLOOD-BRAIN-BARRIER; INSULIN-RECEPTOR SUBSTRATE; AMYLOID PRECURSOR PROTEIN; TYPE-2; DIABETES-MELLITUS; GENOME-WIDE ASSOCIATION; INTRANASAL INSULIN; APOLIPOPROTEIN-E; A-BETA; CHOLESTEROL-METABOLISM; COGNITIVE IMPAIRMENT;
D O I
10.1111/febs.15540
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
'A peculiar severe disease process of the cerebral cortex' are the exact words used by A. Alzheimer in 1906 to describe a patient's increasingly severe condition of memory loss, changes in personality, and sleep disturbance. A century later, this 'peculiar' disease has become widely known as Alzheimer's disease (AD), the world's most common neurodegenerative disease, affecting more than 35 million people globally. At the same time, its pathology remains unclear and no successful treatment exists. Several theories for AD etiology have emerged throughout the past century. In this review, we focus on the metabolic mechanisms that are similar between AD and metabolic diseases, based on the results from genome-wide association studies. We discuss signaling pathways involved in both types of disease and look into new optogenetic methods to study thein vivomechanisms of AD.
引用
收藏
页码:3855 / 3873
页数:19
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