4.7 Article

Quercetin suppresses immune cell accumulation and improves mitochondrial gene expression in adipose tissue of diet-induced obese mice

Journal

MOLECULAR NUTRITION & FOOD RESEARCH
Volume 60, Issue 2, Pages 300-312

Publisher

WILEY-BLACKWELL
DOI: 10.1002/mnfr.201500595

Keywords

Adipose tissue; Inflammation; Obesity; Oxidative stress; Quercetin

Funding

  1. Ministry of Agriculture, Forestry and Fisheries (MAFF)
  2. Research Project on the Development of Agricultural Products and Foods with Health-promoting benefits (NARO)
  3. Ministry of Education, Culture, Sports, Science and Technology, Japan [24501024, 15K00867]
  4. Grants-in-Aid for Scientific Research [24501024, 15K00867] Funding Source: KAKEN

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ScopeTo examine the effect of dietary quercetin on the function of epididymal adipose tissue (EAT) in Western diet-induced obese mice. Methods and resultsC57BL/6J mice were fed a control diet; a Western diet high in fat, cholesterol, and sucrose; or the same Western diet containing 0.05% quercetin for 18 weeks. Supplementation with quercetin suppressed the increase in the number of macrophages, the decrease in the ratio of CD4(+) to CD8(+) T cells in EAT, and the elevation of plasma leptin and tumor necrosis factor levels in mice fed the Western diet. Comprehensive gene expression analysis revealed that quercetin suppressed gene expression associated with the accumulation and activation of immune cells, including macrophages and lymphocytes in EAT. It also improved the expression of the oxidative stress-sensitive transcription factor NFB, NADPH oxidases, and antioxidant enzymes. Quercetin markedly increased gene expression associated with mitochondrial oxidative phosphorylation and mitochondrial DNA content. ConclusionQuercetin most likely universally suppresses the accumulation and activation of immune cells, including antiinflammatory cells, whereas it specifically increased gene expression associated with mitochondrial oxidative phosphorylation. Suppression of oxidative stress and NFB activity likely contributed to the prevention of the accumulation and activation of immune cells and resulting chronic inflammation.

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