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

被引:84
|
作者
Chang, C-J [1 ,2 ,3 ,4 ]
Lu, C-C [5 ]
Lin, C-S [1 ,2 ,3 ,4 ]
Martel, J. [1 ,2 ]
Ko, Y-F [6 ,7 ]
Ojcius, D. M. [1 ,2 ,8 ]
Wu, T-R [3 ]
Tsai, Y-H [3 ]
Yeh, T-S [9 ]
Lu, J-J [3 ,10 ]
Lai, H-C [1 ,2 ,3 ,4 ,10 ,11 ,12 ]
Young, J. D. [1 ,2 ,6 ,7 ,13 ]
机构
[1] Chang Gung Univ, Ctr Mol & Clin Immunol, 259 Wen Hwa First Rd, Taoyuan 33302, Taiwan
[2] Linkou Chang Gung Mem Hosp, Chang Gung Immunol Consortium, Taoyuan, Taiwan
[3] Chang Gung Univ, Coll Med, Dept Med Biotechnol & Lab Sci, 259 Wen Hwa First Rd, Taoyuan 33302, Taiwan
[4] Chang Gung Univ, Res Ctr Bacterial Pathogenesis, Taoyuan, Taiwan
[5] Fu Jen Catholic Univ, Dept Resp Therapy, New Taipei, Taiwan
[6] Chang Gung Biotechnol Corp, Taipei, Taiwan
[7] Ming Chi Univ Technol, Biochem Engn Res Ctr, New Taipei, Taiwan
[8] Univ Pacific, Arthur Dugoni Sch Dent, Dept Biomed Sci, San Francisco, CA USA
[9] Linkou Chang Gung Mem Hosp, Dept Surg, Taoyuan, Taiwan
[10] Linkou Chang Gung Mem Hosp, Dept Lab Med, Taoyuan, Taiwan
[11] Chang Gung Univ Sci & Technol, Coll Human Ecol, Res Ctr Chinese Herbal Med, Taoyuan, Taiwan
[12] Chang Gung Univ Sci & Technol, Coll Human Ecol, Res Ctr Food & Cosmet Safety, Taoyuan, Taiwan
[13] Rockefeller Univ, Cellular Physiol & Immunol Lab, 1230 York Ave, New York, NY 10021 USA
关键词
ACTIVATED PROTEIN-KINASE; INSULIN-RESISTANCE; METABOLIC SYNDROME; ADIPOSE-TISSUE; INFLAMMATION; CAMPHORATA; LINKING; ACID; SENSITIVITY;
D O I
10.1038/ijo.2017.149
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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-1 beta, interleukin-6, tumor necrosis factor-a), 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.
引用
收藏
页码:231 / 243
页数:13
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