ReferenceID 2930

The effects of taraxasterol on liver fibrosis revealed by RNA sequencing

Int Immunopharmacol

Effective treatment of liver fibrosis remains a challenging medical problem. Taraxasterol (TAR) has anti-inflammatory, anti-tumor and hepatoprotective effects. Studies have shown that TAR has good biological activity aga

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Reference Id
2930
Evidence Id
19520
Core Evidence Id
19520
Source Reference Id
5851
Herb2 Reference Id
HBREF006648
Subject Paper Key
HBIN045530_36470119
Pubmed Id
36470119
Doi
10.1016/j.intimp.2022.109481
Paper Title
The effects of taraxasterol on liver fibrosis revealed by RNA sequencing
Paper Abstract
Effective treatment of liver fibrosis remains a challenging medical problem. Taraxasterol (TAR) has anti-inflammatory, anti-tumor and hepatoprotective effects. Studies have shown that TAR has good biological activity against liver injury induced by various factors. However, the anti-fibrotic effect of TAR and its mechanism are never clarified. The purpose of this study was to investigate the effects of TAR in liver fibrosis and to reveal its possible mechanism by RNA sequencing. Our results suggested that TAR attenuated CCl 4 -induced hepatocyte necrosis, inflammatory infiltration and ECM deposition. TAR inhibited the levels of ALT, AST, ALP, γ-GT, LN, HA, PC III and IV-C in serum and TNF-α, IL-6, IL-1β and MDA in liver. In addition, TAR increased the activities of SOD and GSH-Px in liver. RNA sequencing analysis of liver tissues revealed that CCl 4 and TAR significantly altered 4,155 genes and 2,675 genes, respectively. TAR reversed changes in ECM-related genes. More specifically, TAR mediated the expression of genes related to the activation of the Hippo pathway, while inhibiting the expression of genes related to the activation of HIF-1α, TGF-β/Smad, and Wnt pathways. In the validation experiments, the qRT-PCR results showed that the expression levels of Yap1, Tead3, Hif1α, Vegfa, Tgfβ1, Want3a, and Ctnnb1 mRNA were consistent with the RNA sequencing results. The Western blot results showed that TAR inhibited the levels of TGF-β1 and p-Smad2. In addition, the results in vitro were consistent with those in vivo. Therefore, we concluded that TAR improved CCl 4 -induced liver fibrosis by regulating Hippo, HIF-1α, TGF-β/Smad and Wnt pathways.
Journal
Int Immunopharmacol
Publish Year
2022
Experiment Subject
Experiment Type
Cell Experiment
Phenotype Related
Liver Fibrosis; Liver Injury
Paper Title Cn
Paper Title En
The effects of taraxasterol on liver fibrosis revealed by RNA sequencing
Bilingual Status
semi_complete