Contributing Factors to Diabetic Brain Injury and Cognitive Decline

被引:14
作者
Verma, Nirmal [1 ]
Despa, Florin [1 ,2 ]
机构
[1] Univ Kentucky, Coll Med, Dept Pharmacol & Nutr Sci, Wethington Bldg,Room 459,900 S Limestone, Lexington, KY 40536 USA
[2] Univ Kentucky, Dept Neurol, Coll Med, Lexington, KY 40536 USA
基金
美国国家卫生研究院;
关键词
Dementia; Diabetes mellitus; Obesity; ISLET AMYLOID POLYPEPTIDE; GLYCATION END-PRODUCTS; ALZHEIMERS-DISEASE; VASCULAR DEMENTIA; AMYLIN DEPOSITION; IN-VIVO; RISK; DYSFUNCTION; IMPAIRMENT; DISORDERS;
D O I
10.4093/dmj.2019.0153
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The link of diabetes with co-occurring disorders in the brain involves complex and multifactorial pathways. Genetically engineered rodents that express familial Alzheimer's disease-associated mutant forms of amyloid precursor protein and presenilin 1 (PSEN1) genes provided invaluable insights into the mechanisms and consequences of amyloid deposition in the brain. Adding diabetes factors (obesity, insulin impairment) to these animal models to predict success in translation to clinic have proven useful at some extent only. Here, we focus on contributing factors to diabetic brain injury with the aim of identifying appropriate animal models that can be used to mechanistically dissect the pathophysiology of diabetes-associated cognitive dysfunction and how diabetes medications may influence the development and progression of cognitive decline in humans with diabetes.
引用
收藏
页码:560 / 567
页数:8
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