Antrodia cinnamomea reduces obesity and modulates the gut microbiota in high-fat diet-fed mice

Int J Obes (Lond). 2018 Feb;42(2):231-243. doi: 10.1038/ijo.2017.149. Epub 2017 Jun 20.

Abstract

Background: Obesity is associated with gut microbiota dysbiosis, disrupted intestinal barrier and chronic inflammation. Given the high and increasing prevalence of obesity worldwide, anti-obesity treatments that are safe, effective and widely available would be beneficial. We examined whether the medicinal mushroom Antrodia cinnamomea may reduce obesity in mice fed with a high-fat diet (HFD).

Methods: Male C57BL/6J mice were fed a HFD for 8 weeks to induce obesity and chronic inflammation. The mice were treated with a water extract of A. cinnamomea (WEAC), and body weight, fat accumulation, inflammation markers, insulin sensitivity and the gut microbiota were monitored.

Results: After 8 weeks, the mean body weight of HFD-fed mice was 39.8±1.2 g compared with 35.8±1.3 g for the HFD+1% WEAC group, corresponding to a reduction of 4 g or 10% of body weight (P<0.0001). WEAC supplementation reduced fat accumulation and serum triglycerides in a statistically significant manner in HFD-fed mice. WEAC also reversed the effects of HFD on inflammation markers (interleukin-1β, interleukin-6, tumor necrosis factor-α), insulin resistance and adipokine production (leptin and adiponectin). Notably, WEAC increased the expression of intestinal tight junctions (zonula occludens-1 and occludin) and antimicrobial proteins (Reg3g and lysozyme C) in the small intestine, leading to reduced blood endotoxemia. Finally, WEAC modulated the composition of the gut microbiota, reducing the Firmicutes/Bacteroidetes ratio and increasing the level of Akkermansia muciniphila and other bacterial species associated with anti-inflammatory properties.

Conclusions: Supplementation with A. cinnamomea produces anti-obesogenic, anti-inflammatory and antidiabetic effects in HFD-fed mice by maintaining intestinal integrity and modulating the gut microbiota.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antrodia / chemistry*
  • Diet, High-Fat*
  • Disease Models, Animal
  • Dysbiosis / diet therapy*
  • Dysbiosis / physiopathology
  • Gastrointestinal Microbiome / drug effects*
  • Inflammation / diet therapy*
  • Insulin Resistance / physiology
  • Male
  • Medicine, Traditional
  • Mice
  • Mice, Inbred C57BL
  • Obesity / diet therapy*
  • Obesity / physiopathology
  • Plant Extracts / pharmacology*
  • Plants, Medicinal / chemistry*

Substances

  • Plant Extracts