Bridging Type 2 Diabetes and Alzheimer's Disease: Assembling the Puzzle Pieces in the Quest for the Molecules With Therapeutic and Preventive Potential

被引:56
作者
de Matos, Ana Marta [1 ,2 ]
de Macedo, Maria Paula [2 ]
Rauter, Amelia Pilar [1 ]
机构
[1] Univ Lisbon, Fac Ciencias, Ed C8, P-1749016 Lisbon, Portugal
[2] Nova Med Sch, CEDOC Chron Dis, Rua Camara Pestana 6,6-A,Ed CEDOC 2, P-1150082 Lisbon, Portugal
关键词
type; 2; diabetes; diabetes-induced dementia; Alzheimer's disease; natural products; drug design; ISLET AMYLOID POLYPEPTIDE; INSULIN-DEGRADING ENZYME; BLOOD-BRAIN-BARRIER; GLYCOGEN-SYNTHASE KINASE-3; ACTIVATED PROTEIN-KINASE; HIGH-FAT DIET; MILD COGNITIVE IMPAIRMENT; PANCREATIC BETA-CELLS; CHRONIC CEREBRAL HYPOPERFUSION; APOLIPOPROTEIN-E GENOTYPE;
D O I
10.1002/med.21440
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Type 2 diabetes (T2D) and Alzheimer's disease (AD) are two age-related amyloid diseases that affect millions of people worldwide. Broadly supported by epidemiological data, the higher incidence of AD among type 2 diabetic patients led to the recognition of T2D as a tangible risk factor for the development of AD. Indeed, there is now growing evidence on brain structural and functional abnormalities arising from brain insulin resistance and deficiency, ultimately highlighting the need for new approaches capable of preventing the development of AD in type 2 diabetic patients. This review provides an update on overlapping pathophysiological mechanisms and pathways in T2D and AD, such as amyloidogenic events, oxidative stress, endothelial dysfunction, aberrant enzymatic activity, and even shared genetic background. These events will be presented as puzzle pieces put together, thus establishing potential therapeutic targets for drug discovery and development against T2D and diabetes-induced cognitive declinea heavyweight contributor to the increasing incidence of dementia in developed countries. Hoping to pave the way in this direction, we will present some of the most promising and well-studied drug leads with potential against both pathologies, including their respective bioactivity reports, mechanisms of action, and structure-activity relationships.
引用
收藏
页码:261 / 324
页数:64
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