Literature DB >> 15663914

FFAs: do they play a role in vascular disease in the insulin resistance syndrome?

Sudha S Shankar1, Helmut O Steinberg.   

Abstract

The insulin resistance syndrome, otherwise known as the metabolic syndrome, describes a cluster of cardiovascular and metabolic abnormalities, which are strongly associated with overweight and obesity. The importance of the syndrome is due to its increased rates of cardiovascular morbidity and mortality. Insulin resistance is also characterized by elevated free fatty acid (FFA) levels. In otherwise healthy human subjects, elevation of FFA impairs endothelial function. This appears to be largely the result of blunting of nitric oxide-dependent tone, most likely at the level of the endothelial isoform of nitric oxide synthase (eNOS). Some of the potential mediatory mechanisms include oxidative stress, proinflammatory cytokines, C-reactive protein, or endogenous inhibitors of eNOS. Regardless of the mechanism(s) that mediates the effects of increased FFA on the vasculature, impaired vascular function is likely to account, at least in part, for the increase in cardiovascular mortality in subjects with the insulin resistance syndrome.

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Year:  2005        PMID: 15663914     DOI: 10.1007/s11892-005-0064-6

Source DB:  PubMed          Journal:  Curr Diab Rep        ISSN: 1534-4827            Impact factor:   4.810


  37 in total

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Journal:  Am J Physiol       Date:  1994-08

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Journal:  J Clin Invest       Date:  1999-01       Impact factor: 14.808

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  11 in total

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Authors:  Kathleen M Eyster; Connie J Mark; Richard Gayle; Douglas S Martin
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6.  Signaling mechanisms involved in altered function of macrophages from diet-induced obese mice affect immune responses.

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7.  The metabolic profile in patients with skin tags.

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Authors:  April C Inyard; Daniel G Chong; Alexander L Klibanov; Eugene J Barrett
Journal:  Diabetes       Date:  2009-08-12       Impact factor: 9.461

9.  FABP4 dynamics in obesity: discrepancies in adipose tissue and liver expression regarding circulating plasma levels.

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10.  Palmitate diet-induced loss of cardiac caveolin-3: a novel mechanism for lipid-induced contractile dysfunction.

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