4.7 Article

Effects of Poria cocos extract on metabolic dysfunction-associated fatty liver disease via the FXR/PPARa-SREBPs pathway

期刊

FRONTIERS IN PHARMACOLOGY
卷 13, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2022.1007274

关键词

MAFLD (metabolic-associated fatty liver disease); Poria cocos (Schw) Wolf; bile acid metabolism; FXRP/PAR alpha-SREBP pathway; lipid homeostasis; UPLC Q-TOF/MS

资金

  1. Application and Basis Research Project of Yunnan China
  2. National Natural Science Foundation of China [2019IB009, 202002AA100007, 202001AZ070001-043, 202201AW070016, 2022Y345, 202105AG070012]
  3. High-level TCM talents (reserve talents) project of Yunnan [82160748, 82104381]
  4. [1]

向作者/读者索取更多资源

Poria cocos ethanol extract shows a protective effect on high-fat diet-induced fatty liver disease by reducing lipid accumulation and inflammation and improving lipid metabolism. Poricoic acid B and polyporenic acid C, the major active compounds in Poria cocos, contribute to its therapeutic effect by activating the nuclear receptor PPAR alpha.
Despite the increase in the global prevalence of metabolic dysfunction-associated fatty liver disease (MAFLD), no approved drug currently exists for the disease. Poria cocos (Schw.) Wolf (P. cocos) is a medicinal mushroom belonging to a family of polyporaceae widely used in TCM clinics to protect the liver and treat obesity. However, its efficacy, practical components, and underlying mechanism against MAFLD are yet to be determined. In this study, we evaluated the effects of Poria cocos (P. cocos) ethanol extract (EPC) on hepatic dyslipidemia, steatosis, and inflammation by both bioinformatics analysis and MAFLD rats induced by HFD feeding. We found EPC treatment dramatically reduced lipid accumulation, inflammatory cell infiltration, and liver injury. EPC reduced serum TC, TG levels, and hepatic TG, TBA, and NEFA contents. UHPLC Q-Trap/MS examination of BA profiles in serum and feces showed that EPC increased fecal conjugated BAs, decreased free BAs, and improved BA metabolism in HFD-fed rats. Western blot and RT-qPCR analysis showed that EPC could activate hepatic FXR and PPAR alpha expression and reduce CYP7A1 and SREBP-1c expression. Systemic pharmacology combined with molecular docking suggested that poricoic acid B and polyporenic acid C, the major active compounds in EPC, could ameliorate lipid homeostasis by activating the nuclear receptor PPAR alpha. We further confirmed their inhibition effects of lipid droplet deposition in steatized L-02 hepatocytes. In summary, EPC alleviated HFD-induced MAFLD by regulating lipid homeostasis and BA metabolism via the FXR/PPAR alpha-SREBPs signaling pathway. P. cocos triterpenes, such as poricoic acid B and polyporenic acid C, were the characteristic substances of P. cocos for the treatment of MAFLD.

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