2014
DOI: 10.1038/ijo.2014.181
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Effect of resveratrol on visceral white adipose tissue inflammation and insulin sensitivity in a mouse model of sleep apnea

Abstract: Resveratrol does not reverse the SF-induced increases in food intake and weight gain, but markedly attenuates VWAT inflammation and insulin resistance, thereby providing a potentially useful adjunctive therapy in the context of sleep disorders manifesting metabolic morbidity.

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Cited by 39 publications
(26 citation statements)
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References 39 publications
(36 reference statements)
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“…Concerning the effect of RSV on serum glucose and albumin, previous studies agreed to our results regarding both parameters (Das et al, 2010;Movahed et al, 2013). Other studies have also noted that RSV improved insulin sensitivity in experimental mice (Carreras et al, 2015). Mechanisms may include RSV activation of AMP-activated protein kinase C and SIRT1 (Deng et al, 2007;Pfluger et al, 2008;Tamaki et al, 2014).…”
Section: Discussionsupporting
confidence: 81%
“…Concerning the effect of RSV on serum glucose and albumin, previous studies agreed to our results regarding both parameters (Das et al, 2010;Movahed et al, 2013). Other studies have also noted that RSV improved insulin sensitivity in experimental mice (Carreras et al, 2015). Mechanisms may include RSV activation of AMP-activated protein kinase C and SIRT1 (Deng et al, 2007;Pfluger et al, 2008;Tamaki et al, 2014).…”
Section: Discussionsupporting
confidence: 81%
“…We conducted a series of experiments [11,12] to confirm that resveratrol can effectively suppress the body's response to inflammation and reduce inflammatory injury. The results are consistent with those of other studies [13,14].…”
Section: Introductionsupporting
confidence: 83%
“…Treatment of hepatocytes with PDX suppressed palmitate‐induced fetuin‐A and SeP expression in a dose and time‐dependent manner (Figure A,B). AMPK and SIRT1 may have therapeutic importance for treating obesity and insulin resistance. Consistent with previous findings, PDX induces AMPK phosphorylation and SIRT1 expression in a dose‐dependent fashion in primary hepatocytes (Figure C,D).…”
Section: Resultsmentioning
confidence: 99%