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  4. The role of oxidative stress in the pathogenesis of type 2 diabetes: From molecular mechanism to clinical implication
 
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The role of oxidative stress in the pathogenesis of type 2 diabetes: From molecular mechanism to clinical implication

Journal
American Journal of Translational Research
Journal Volume
2
Journal Issue
3
Pages
316-331
Date Issued
2010
Author(s)
YI-CHENG CHANG  
LEE-MING CHUANG  
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-77954672012&partnerID=40&md5=732cf6d144714a2ab8d55dc934f51ec5
https://scholars.lib.ntu.edu.tw/handle/123456789/495516
Abstract
A surplus of food supply has evoked a worldwide increase in incidence of type 2 diabetes. This trend will have a significant impact on the life span of people living in modern societies. In contrast, reduced calorie intake has significant impact on preventing type 2 diabetes and increasing longevity. Increased production of reactive oxygen species (ROS), resulting in oxidative stress, has long been proposed as a unifying mechanism linking nutrient excessand diabetes. This review describes the updated mechanism by which oxidative stress provoked by nutrient excess contributes to the development of insulin resistance and pancreatic beta-cell failure. However, despite the promising results in cellular and animal models, major clinical trials have failed to demonstrate beneficial effect of antioxidants on the prevention of type 2 diabetes or the degree of glycemic control in individuals with diabetes. Emerging evidence shows that ROS also function as an insulin-signaling molecule in normal physiology and casts doubt on the potential beneficial effect of antioxidants. The gap between basic research and clinical outcomes heightens the importance for elucidating the precise molecular mechanisms by which cellular redox status affects insulin signaling.
SDGs

[SDGs]SDG3

Other Subjects
alpha tocopherol; antioxidant; ascorbic acid; beta carotene; chaperone; hydrogen peroxide; insulin; manganese superoxide dismutase; reactive oxygen metabolite; selenium; taurine; thioctic acid; thioredoxin peroxidase; transcription factor; zinc; clinical trial; diabetic patient; gluconeogenesis; glucose homeostasis; glucose metabolism; glycemic control; glycogenolysis; human; hyperglycemia; inflammation; insulin resistance; mitochondrial respiration; molecular dynamics; non insulin dependent diabetes mellitus; nonhuman; nutrient; oxidation reduction potential; oxidative phosphorylation; oxidative stress; pancreas islet beta cell; pathogenesis; regulatory mechanism; review; signal transduction; therapy effect; vitamin supplementation; Animalia
Type
review

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