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Apple polyphenol extract alleviates lipid accumulation in free‐fatty‐acid‐exposed <scp>HepG2</scp> cells via activating autophagy mediated by <scp>SIRT1</scp>/<scp>AMPK</scp> signaling

Deming Li, Yuan‐Lu Cui, Xinjing Wang, Fang Liu, Xinli Li

2020Phytotherapy Research51 citationsDOI

Abstract

Defective degradation of intracellular lipids induced by autophagy is causally linked to the development of non-alcoholic fatty liver disease (NAFLD). Natural agents that can restore autophagy could therefore have the potentials for clinical applications for this public health issue. Herein, we investigated the effects of apple polyphenol extract (APE) on fatty acid-induced lipids depositions in HepG2 cells. APE treatment alleviated palmitic acid and oleic acid-induced intracellular lipid accumulation, concomitant with the increased autophagy, restored lysosomal acidification, inhibited lipid synthesis and slight promotion of fatty acid oxidation. Mechanistically, APE up-regulated the expression of SIRT1, activated LKB1/AMPK pathway and inhibited mTOR signaling. Over-expressed or knock-down SIRT1 positively regulated AMPK and ATG7 expressions. SIRT1 and ATG7 knock-down impaired APE induction of improved lipid accumulation, increased intracellular TG content. Thus, APE induction of autophagy to ameliorate fatty acid-induced lipid deposition is SIRT1 dependent, APE conserved preventive potentials for clinical hepatosteatosis.

Topics & Concepts

AutophagyAMPKIntracellularLipid dropletChemistryOleic acidBiochemistryFatty acidPalmitic acidBeta oxidationFatty liverAMP-activated protein kinaseCell biologyBiologyProtein kinase AKinaseApoptosisMedicineInternal medicineDiseaseAutophagy in Disease and TherapySirtuins and Resveratrol in MedicineLipid metabolism and biosynthesis
Apple polyphenol extract alleviates lipid accumulation in free‐fatty‐acid‐exposed <scp>HepG2</scp> cells via activating autophagy mediated by <scp>SIRT1</scp>/<scp>AMPK</scp> signaling | Litcius