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Hypolipogenic effects of Icariside E4 via phosphorylation of AMPK and inhibition of MID1IP1 in HepG2 cells.

Abstract
Though icariside E4 (IE4) is known to have anti-noceptive, anti-oxidant, anti-Alzheimer and anti-inflammatory effects, there was no evidence on the effect of IE4 on lipid metabolism so far. Hence, the hypolipogenic mechanism of IE4 was investigated in HepG2 hepatocellular carcinoma cells (HCCs) in association with MID1 Interacting Protein 1(MID1IP1) and AMPK signaling. Here, IE4 did not show any toxicity in HepG2 cells, but reduced lipid accumulation in HepG2 cells by Oil Red O staining. MID1IP1 depletion decreased the expression of SREBP-1c and fatty acid synthase (FASN) and induced phosphorylation of ACC in HepG2 cells. Indeed, IE4 activated phosphorylation of AMPK and ACC and inhibited the expression of MID1IP1 in HepG2 cells. Furthermore, IE4 suppressed the expression of SREBP-1c, liver X receptor-α (LXR), and FASN for de novo lipogenesis in HepG2 cells. Interestingly, AMPK inhibitor compound C reversed the ability of IE4 to reduce MID1IP1, SREBP-1c, and FASN and activate phosphorylation of AMPK/ACC in HepG2 cells, indicating the important role of AMPK/ACC signaling in IE4-induced hypolipogenic effect. Taken together, these findings suggest that IE4 has hypolipogenic potential in HepG2 cells via activation of AMPK and inhibition of MID1IP1 as a potent candidate for treatment of fatty liver disease.
AuthorsJin Young Suh, Hyo-Jung Lee, Deok Yong Sim, Ji Eon Park, Chi-Hoon Ahn, Su-Yeon Park, Nari Shin, Bonglee Kim, Bum Sang Shim, Sung-Hoon Kim
JournalPhytotherapy research : PTR (Phytother Res) Vol. 37 Issue 1 Pg. 7-14 (Jan 2023) ISSN: 1099-1573 [Electronic] England
PMID35916211 (Publication Type: Journal Article)
Copyright© 2022 John Wiley & Sons Ltd.
Chemical References
  • Mid1ip1
  • AMP-Activated Protein Kinases
  • icariside E4
  • Sterol Regulatory Element Binding Protein 1
  • Fatty Acid Synthases
Topics
  • Humans
  • Hep G2 Cells
  • Phosphorylation
  • AMP-Activated Protein Kinases (metabolism)
  • Sterol Regulatory Element Binding Protein 1 (metabolism)
  • Lipid Metabolism
  • Lipogenesis
  • Fatty Acid Synthases (metabolism)
  • Liver

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