4.7 Article

(+)-Dehydrovomifoliol Alleviates Oleic Acid-Induced Lipid Accumulation in HepG2 Cells via the PPARα-FGF21 Pathway

Journal

FRONTIERS IN PHARMACOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2021.750147

Keywords

artemisia frigida; non-alcoholic fatty liver disease; peroxisome proliferator-activated receptora; lipid accumulation; terpene

Funding

  1. National Natural Science Foundation of China [81903514]
  2. Opening Project for the first-class disciplines of pharmacy at Hunan University of Chinese Medicine [2020YX03]
  3. Scientific research project of Education Department of Zhejiang Province [Y202146053]

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The compound (+)-dehydrovomifoliol isolated from Artemisia frigida showed potent effects against lipid accumulation in HepG2 cells induced by oleic acid. It also affected hepatic lipogenesis and fatty acid oxidation signaling, suggesting it could be a promising lead compound for developing new drugs for NAFLD prevention.
An overload of hepatic fatty acids, such as oleic acid is a key trigger of non-alcoholic fatty liver disease (NAFLD). Here, we investigated whether Artemisia frigida, a valuable traditional medicine used to treat various diseases, could mitigate OA-induced lipid accumulation in HepG2 cells. Then, to identify the active substances in A. frigida, a phytochemistry investigation was conducted using a bioassay-guided isolation method. Consequently, one terpene (1) and one flavone (2) were identified. Compound 1 ((+)-dehydrovomifoliol) exhibited potent effects against lipid accumulation in OAinduced HepG2 cells, without causing cyto-toxicity. Notably, treatment with (+)-dehydrovomifoliol decreased the expression levels of three genes related to lipogenesis (SREBP1, ACC, and FASN) and increased those of three genes related to fatty acid oxidation (PPARa, ACOX1, and FGF21). In addition, similar results were observed for SREBP1, PPAR alpha, and FGF21 protein levels. The effects of (+)-dehydrovomifoliol were partially reversed by treatment with the PPARa antagonist GW6471, indicating the important role of the PPAR alpha-FGF21 axis in the effects of (+)-dehydrovomifoliol. Based on its effects on hepatic lipogenesis and fatty acid oxidation signaling via the PPARa-FGF21 axis, (+)-dehydrovomifoliol isolated from A. frigida could be a useful early lead compound for developing new drugs for NAFLD prevention.

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