4.7 Article

Hepatoprotective effect of curcumin against bisphenol A-induced hepatic steatosis via modulating gut microbiota dysbiosis and related gut-liver axis activation in CD-1 mice

期刊

JOURNAL OF NUTRITIONAL BIOCHEMISTRY
卷 109, 期 -, 页码 -

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jnutbio.2022.109103

关键词

Curcumin; Bisphenol A; Hepatic steatosis; Gut microbiota; Toll-like receptor 4; nuclear factor-KB

资金

  1. National Nat- ural Science Foundation of China [81973019]
  2. Natural Sci- ence Foundation of Guangdong Province [2022A1515011610, 2020A1515011167, 2018A030313782]
  3. Medical Science and Technology Foundation of Guangdong Province [A2018482, A2019127]

向作者/读者索取更多资源

Chronic exposure to low-dose bisphenol A (BPA) is a global public health concern that may result in gut microbial dysbiosis and hepatic steatosis. Curcumin, extracted from turmeric, has been found to alleviate BPA-induced hepatic steatosis by improving the intestinal flora and modulating the gut-liver axis.
Chronic exposure to low-dose bisphenol A (BPA) has become a global problem of public health. Our previous work showed that low-dose BPA exposure caused gut microbial dysbiosis and hepatic steatosis. Curcumin, a polyphenol extracted from turmeric, has an inhibitory effect on liver lipid accumulation, whether curcumin can alleviate BPA-induced hepatic steatosis through improving intestinal flora and modulating gut-liver axis remains to be elucidated. Male CD-1 mice were fed with BPA-contaminated diet supplemented with or not with curcumin for 24 weeks. Curcumin supplementation markedly ame-liorated liver fat accumulation and hepatic steatosis induced by BPA. Gut microbiota analysis via 16S rRNA sequencing revealed that the relative abundance of Proteobacteria and Firmicutes/Bacteroidetes ratio were increased in BPA-fed mice, and this alteration was reversed by curcumin treatment. Akkermansia, which was recognized as a potential probiotic, was significantly reduced after BPA exposure and was restored to the control level with curcumin addition. Furthermore, curcumin supplementation reversed the down-regulation of intestinal tight junction protein expressions (zona occludens-1 and occludin), im-proved increased gut permeability, reduced serum lipopolysaccharide level and suppressed the activation of hepatic toll-like receptor 4 / nuclear factor -KB (TLR4/NF-KB) pathway induced by BPA. These results indicated that the protective effect of curcumin against hepatic steatosis induced by BPA and further revealed that its mechanism might be its prebiotic effect on maintaining intestinal flora homeostasis and improving intestinal barrier function, consequently reducing serum lipopolysaccharide-triggered inflammatory response in the liver. Our work provides evidence for curcumin as a potential nutritional therapy for BPA-mediated hepatic steatosis. (C) 2022 Elsevier Inc. All rights reserved.

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