Literature DB >> 22305519

Linking mitochondrial bioenergetics to insulin resistance via redox biology.

Kelsey H Fisher-Wellman1, P Darrell Neufer.   

Abstract

Chronic overnutrition and physical inactivity are major risk factors for insulin resistance and type 2 diabetes. Recent research indicates that overnutrition generates an increase in hydrogen peroxide (H(2)O(2)) emission from mitochondria, serving as a release valve to relieve the reducing pressure created by fuel overload, as well as a primary signal that ultimately decreases insulin sensitivity. H(2)O(2) is a major input to cellular redox circuits that link to cysteine residues throughout the entire proteome to regulate cell function. Here we review the principles of mitochondrial bioenergetics and redox systems biology and offer new insight into how H(2)O(2) emission may be linked via redox biology to the etiology of insulin resistance. Copyright Â
© 2011 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22305519      PMCID: PMC3313496          DOI: 10.1016/j.tem.2011.12.008

Source DB:  PubMed          Journal:  Trends Endocrinol Metab        ISSN: 1043-2760            Impact factor:   12.015


  88 in total

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  137 in total

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2.  Mitochondrial dysfunction in white adipose tissue.

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8.  Restoring redox balance enhances contractility in heart trabeculae from type 2 diabetic rats exposed to high glucose.

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9.  Hepatocyte glutathione peroxidase-1 deficiency improves hepatic glucose metabolism and decreases steatohepatitis in mice.

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10.  Mitochondrial metabolism mediates oxidative stress and inflammation in fatty liver.

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