4.6 Article

Quercetin reduces obesity-associated ATM infiltration and inflammation in mice: a mechanism including AMPKα1/SIRT1

Journal

JOURNAL OF LIPID RESEARCH
Volume 55, Issue 3, Pages 363-374

Publisher

ELSEVIER
DOI: 10.1194/jlr.M038786

Keywords

obesity; insulin resistance; adipose tissue macrophage; macrophages; adenosine monophosphate-activated protein kinase alpha 1/silent information regulator 1

Funding

  1. National Natural Science Foundation of China [31171315]
  2. Specialized Research Fund for the Doctoral Program of Higher Education of China [20100111110009]
  3. Anhui Provincial Natural Science Foundation of China [11040606M92]
  4. Fundamental Research Funds for the Central Universities, China [2012HGCX0003, 2012HGQC0019]
  5. China Postdoctoral Science Foundation [2013M541817]

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Adipose tissue macrophage (ATM) plays a central role in obesity-associated inflammation and insulin resistance. Quercetin, a dietary flavonoid, possesses anti-inflammation and anti-insulin resistance properties. However, it is unclear whether quercetin can alleviate high-fat diet (HFD)-induced ATM infiltration and inflammation in mice. In this study, 5-week-old C57BL/6 mice were fed low-fat diet, HFD, or HFD with 0.l% quercetin for 12 weeks, respectively. Dietary quercetin reduced HFD-induced body weight gain and improved insulin sensitivity and glucose intolerance in mice. Meanwhile, dietary quercetin enhanced glucose transporter 4 translocation and protein kinase B signal in epididymis adipose tissues (EATs), suggesting that it heightened glucose uptake in adipose tissues. Histological and real-time PCR analysis revealed that quercetin attenuated mast cell and macrophage infiltration into EATs in HFD-fed mice. Dietary quercetin also modified the phenotype ratio of M1/M2 macrophages, lowered the levels of proinflammatory cytokines, and enhanced adenosine monophosphate-activated protein kinase (AMPK) alpha 1 phosphorylation and silent information regulator 1 (SIRT1) expression in EATs. Further, using AMPK activator 5-aminoimidazole-4-carboxamide-1-beta 4-ribofuranoside and inhibitor Compound C, we found that quercetin inhibited polarization and inflammation of mouse bone marrow-derived macrophages through an AMPK alpha 1/SIRT1-mediated mechanism.(jlr) In conclusion, dietary quercetin might suppress ATM infiltration and inflammation through the AMPK alpha 1/SIRT1 pathway in HFD-fed mice

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