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The protective role of protocatechuic acid against chemically induced liver fibrosis in vitro and in vivo.
Cui, Bo; Yang, Zhe; Wang, Shuning; Guo, Mengnan; Li, Qianqian; Zhang, Qiuhua; Bi, Xiuli.
Afiliação
  • Cui B; College of Life Science, Liaoning University, Shenyang, China.
  • Yang Z; College of Life Science, Liaoning University, Shenyang, China.
  • Wang S; College of Life Science, Liaoning University, Shenyang, China.
  • Guo M; College of Life Science, Liaoning University, Shenyang, China.
  • Li Q; College of Life Science, Liaoning University, Shenyang, China.
  • Zhang Q; Department of Pharmacology, Liaoning University of Traditional Chinese Medicine, Liaoning University, Shenyang, China.
  • Bi X; Department of Pharmacology, Liaoning University of Traditional Chinese Medicine, Liaoning University, Shenyang, China; Research Center for Computer Simulating and Information Processing of Bio-macromolecules of Liaoning Province, Liaoning University, Shenyang, China; ; xiulibi@lnu.edu.cn, Email: xiu
Pharmazie ; 76(5): 232-238, 2021 05 01.
Article em En | MEDLINE | ID: mdl-33964998
ABSTRACT
Liver fibrosis is the result of long-term liver injury and has a high incidence worldwide. Protocatechuic acid (PCA) is ubiquitous in vegetables, nuts, brown rice and herbal medicines, which is reported to possess anti-asthmatic, anti-cancer, and anti-oxidation properties. Our research aimed to investigate the effect of PCA on liver fibrosis. In vitro, TNF-α-induced hepatic stellate cell (HSC) model was used to assess the anti-fibrosis effects of PCA. In vivo, mice were treated with thioacetamide (TAA) to develop liver fibrosis. Body weight, organ index, histological changes, and proteins alteration of factors associated with TGF-ß signaling pathway were used to assess the anti-fibrosis effects of PCA. Our results showed that PCA not only inhibited cell viability in TNF-α activated HSC-T6 cells in vitro, but also efficiently mitigated TAA-induced liver damage and fibrosis in vivo. Further experiments indicated that PCA played a protective role in liver fibrosis through regulation of the TGF-ß signaling pathway downregulating the protein expression of p-Smad2, p-ERK, c-Jun. In summary, our findings provide a pharmacological justification for the clinical application of PCA in preventing or treating liver fibrosis.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hidroxibenzoatos / Cirrose Hepática Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hidroxibenzoatos / Cirrose Hepática Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2021 Tipo de documento: Article