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Neochlorogenic Acid Attenuates Hepatic Lipid Accumulation and Inflammation via Regulating miR-34a In Vitro

Meng-Hsun Yu, Tung‐Wei Hung, Chi‐Chih Wang, Chi-Chih Wang, Sheng‐Wen Wu, Tzu‐Wei Yang, Ching-Yu Yang, Tsui‐Hwa Tseng, Chau‐Jong Wang, Chau‐Jong Wang

2021International Journal of Molecular Sciences74 citationsDOIOpen Access PDF

Abstract

Neochlorogenic acid (5-Caffeoylquinic acid; 5-CQA), a major phenolic compound isolated from mulberry leaves, possesses anti-oxidative and anti-inflammatory effects. Although it modulates lipid metabolism, the molecular mechanism is unknown. Using an in-vitro model of nonalcoholic fatty liver disease (NAFLD) in which oleic acid (OA) induced lipid accumulation in HepG2 cells, we evaluated the alleviation effect of 5-CQA. We observed that 5-CQA improved OA-induced intracellular lipid accumulation by downregulating sterol regulatory element-binding protein 1 (SREBP1) and fatty acid synthase (FASN) expression, which regulates the fatty acid synthesis, as well as SREBP2 and HMG-CoA reductases (HMG-CoR) expressions, which regulate cholesterol synthesis. Treatment with 5-CQA also increased the expression of fatty acid β-oxidation enzymes. Remarkably, 5-CQA attenuated OA-induced miR-34a expression. A transfection assay with an miR-34a mimic or miR-34a inhibitor revealed that miR-34a suppressed Moreover, Sirtuin 1 (SIRT1) expression and inactivated 5' adenosine monophosphate-activated protein kinase (AMPK). Our results suggest that 5-CQA alleviates lipid accumulation by downregulating miR-34a, leading to activation of the SIRT1/AMPK pathway.

Topics & Concepts

AMPKFatty acid synthaseChemistrySirtuin 1Lipid metabolismBiochemistryBeta oxidationFatty acidAMP-activated protein kinaseNonalcoholic fatty liver diseaseProtein kinase AKinaseDownregulation and upregulationFatty liverInternal medicineMedicineDiseaseGenePeroxisome Proliferator-Activated ReceptorsGinger and Zingiberaceae researchCancer-related molecular mechanisms research
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