Diosmetin Protects Against Obesity and Metabolic Dysfunctions Through Activation of Adipose Estrogen Receptors in Mice

Mol Nutr Food Res. 2021 Sep;65(17):e2100070. doi: 10.1002/mnfr.202100070. Epub 2021 Jul 14.

Abstract

Scope: Obesity is a major public health and economic problem of global significance. Here, we investigate the role of diosmetin, a natural flavonoid presents mainly in citrus fruits, in the regulation of obesity and metabolic dysfunctions in mice.

Methods and results: Eight-week-old male C57BL/6 mice fed a high-fat diet (HFD) or 5-week-old male ob/ob mice fed a normal diet are treated with diosmetin (50 mg kg-1 daily) or vehicle for 8 weeks. Diosmetin treatment decreases body weight and fat mass, improves glucose tolerance and insulin resistance in obese mice. These metabolic benefits are mainly attributed to increase energy expenditure via enhancing thermogenesis in brown adipose tissue (BAT) and browning of white adipose tissue (WAT). Mechanistically, diosmetin acts as an agonist for estrogen receptors (ERs), and subsequently elevates adipose expressions of ERs in mice and in cultured adipocytes. When ERs are blocked by their antagonist fulvestrant in mice, diosmetin loses its beneficial effects, suggesting that ERs are indispensable for the metabolic benefits of diosmetin.

Conclusion: The results indicate that diosmetin may be a potential anti-obesity nutritional supplement and could be explored for low ERs-related obesity populations.

Keywords: diosmetin; estrogen receptor α (ERα); estrogen receptor β (ERβ); metabolic dysfunctions; obesity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes, White / drug effects
  • Adipocytes, White / metabolism
  • Adipose Tissue, Brown / drug effects*
  • Adipose Tissue, Brown / metabolism
  • Animals
  • Anti-Obesity Agents / pharmacology*
  • Diet, High-Fat / adverse effects
  • Energy Metabolism / drug effects
  • Flavonoids / pharmacology*
  • Glucose Intolerance / prevention & control
  • Inflammation / prevention & control
  • Insulin Resistance
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Obese
  • Obesity / etiology
  • Obesity / genetics
  • Obesity / prevention & control*
  • Receptors, Estrogen / metabolism*
  • Thermogenesis / drug effects

Substances

  • Anti-Obesity Agents
  • Flavonoids
  • Receptors, Estrogen
  • diosmetin