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  2. Total Flavonoids of Engelhardia roxburghiana Wall. Leaves Alleviated Foam Cells Formation through AKT/mTOR-Mediated Autophagy in the Progression of Atherosclerosis

Total Flavonoids of Engelhardia roxburghiana Wall. Leaves Alleviated Foam Cells Formation through AKT/mTOR-Mediated Autophagy in the Progression of Atherosclerosis

  • Chem Biodivers. 2021 Sep;18(9):e2100308. doi: 10.1002/cbdv.202100308.
Jie Wei 1 Liangliang Huang 2 Dongmei Li 1 Junhui He 1 Yanjing Li 3 Fei He 1 Weirong Fang 2 Guining Wei 1
Affiliations

Affiliations

  • 1 Department of Pharmacology, Guangxi Institute of Chinese Medicine and Pharmaceutical Science, Nanning, 530022, P. R. China.
  • 2 State Key Laboratory of Natural Medicines, School of Basic Medical Sciences and Clinical Pharmacy, China Pharmaceutical University, Nanjing, 210009, P. R. China.
  • 3 Guangxi Key Laboratory of Traditional Chinese Medicine Quality Standards, Nanning, 530022, P. R. China.
Abstract

Engelhardia roxburghiana Wall. is a traditional Chinese medicine used for treating cardiovascular diseases. Our previous study has implicated potential effects of total Flavonoids of Engelhardia roxburghiana Wall. (TFER) against hyperlipidemia. The aim of the study is to uncover the effects and underlying mechanisms of TFER on foam cells formation after atherosclerosis. We used high fat diet (HFD) induced Apoe-/- mice and oxidized density lipoprotein (ox-LDL) induced THP-1 cells to mimic process of atherosclerosis in vivo and in vitro, respectively. Lipid accumulation, inflammation response, autophagosomes formation and expressions of Autophagy related target genes were assessed. Our present study demonstrated TFER (500 mg/kg) alleviated macrophage infiltration and lipid accumulation in thoracic aortas of HFD-treated mice. In ox-LDL-treated THP-1 cells, MDC staining and Western blot analysis all indicated that the TFER (200 μg/ml) reduced foam cells formation and IL-1β releasing, activated Autophagy through suppressing Akt/mTOR signaling, significantly regulating expressions of Akt, p-AKT, mTOR, p-mTOR, Beclin 1, LC3-II, p62. It is suggested that TFER alleviated atherosclerosis progression in vivo and in vitro through reducing foam cells formation and inflammatory responses, and the possible mechanism may be due to the activation of macrophage Autophagy by inhibiting Akt and mTOR phosphorylation.

Keywords

AKT/mTOR; atherosclerosis; foam cell formation; macrophagy autophagy; total flavonoids of Engelhardia roxburghiana leaves.

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