Abstract

Abnormal and excessive accumulation of lipid droplets within hepatic cells is the main feature of steatosis and nonalcoholic fatty liver disease (NAFLD) or metabolic-associated fatty liver disease (MAFLD). Dysregulation of lipogenesis contributes to hepatic steatosis and plays an essential role in the pathological progress of MAFLD. Tanshinone IIA is a bioactive phytochemical isolated from Salvia miltiorrhiza Bunge and exhibits anti-inflammatory, antiatherosclerotic and antihyperlipidemic effects. In this study, we aimed to investigate the lipid-lowering effects of tanshinone IIA on the regulation of lipogenesis, lipid accumulation, and the underlying mechanisms in hepatic cells. We demonstrated that tanshinone IIA can significantly inhibit the gene expression involved in de novo lipogenesis including FASN, ACC1, and SCD1, in HepG2 and Huh 7 cells. Tanshinone IIA could increase phosphorylation of ACC1 protein in HepG2 cells. We further demonstrated that tanshinone IIA also could suppress the fatty-acid-induced lipogenesis and TG accumulation in HepG2 cells. Furthermore, tanshinone IIA markedly downregulated the mRNA and protein expression of SREBP1, an essential transcription factor regulating lipogenesis in hepatic cells. Moreover, we found that tanshinone IIA attenuated liver X receptor α (LXRα)-mediated lipogenic gene expression and lipid droplet accumulation, but did not change the levels of LXRα mRNA or protein in HepG2 cells. The molecular docking data predicted tanshinone IIA binding to the ligand-binding domain of LXRα, which may result in the attenuation of LXRα-induced transcriptional activation. Our findings support the supposition that tanshinone IIA possesses a lipid-modulating effect that suppresses lipogenesis and attenuates lipid accumulation by modulating the LXRα/SREBP1 pathway in hepatic cells. Tanshinone IIA can be potentially used as a supplement or drug for the prevention or treatment of MAFLD.

Highlights

  • We found that tanshinone IIA (5 and 10 μM) decreased the amount of nuclear mature sterol regulatory element binding protein 1 (SREBP1) protein by 0.73 ± 0.19- and Biomedicines 2021, 9,0.35

  • We found that tanshinone IIA did not IIA on liver X receptor α (LXRα)-mediated SREBP1 expression, we first examined whether tanshinone IIA

  • These results revealed that tanshinone IIA can inhibit the transcription of fatty-acid synthase (FASN), acetyl-CoA carboxylase 1 (ACC1), and stearoyl-CoA desaturase 1 (SCD1) via the modulation of nuclear SREBP1 levels in hepatic cells

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Summary

Introduction

The disruption of hepatic lipid homeostasis, such as that realized when balance between lipid acquisition through fatty-acid uptake and de novo lipogenesis is disrupted, and lipid deposition may lead to fat retention within the liver and the consequential development of nonalcoholic fatty liver disease (NAFLD), renamed as metabolic-associated fatty liver disease (MAFLD) [2,3,4,5]. Biomedicines 2021, 9, 326 disease worldwide, and it can cause deleterious clinical problems, including end-stage liver diseases and cancer, in some cases. MAFLD manifests in liver conditions ranging from simple triglyceride (TG) and cholesterol accumulation to steatosis. Abnormal and excessive lipid accumulation in the liver has the potential to induce inflammatory injury in hepatocytes and lead to nonalcoholic steatohepatitis (NASH). The development of therapeutic compounds for MAFLD is currently being actively pursued [10,11]

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