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Protective mechanisms of medicinal plants targeting hepatic stellate cell activation and extracellular matrix deposition in liver fibrosis

  • Florent Duval
    ,
  • ,
  • María Teresa González-Garza
    ,
  • Carlos Rodríguez-Montalvo
    ,
  • Delia Elva Cruz-Vega(corresponding author)
*Corresponding author for this work
  • Instituto Tecnologico de Estudios Superiores de Monterrey
    ,
  • Cell Therapy Department
    ,
  • HSJ
Research Output:
Contribution to journal
Article
Peer-review

Open access

Publication metrics

Metrics

SciVal
Citations
27
SciVal
FWCI
1.21
SciVal
Author count
5
SciVal
Paper percentile
76
Scopus
Citations

Abstract

During chronic liver injury, hepatic stellate cells (HSC) are activated and proliferate, which causes excessive extracellular matrix (ECM) deposition, leading to scar formation and fibrosis. Medicinal plants are gaining popularity as antifibrotic agents, and are often safe, cost-effective, and versatile. This review aims to describe the protective role and mechanisms of medicinal plants in the inhibition of HSC activation and ECM deposition during the pathogenesis of liver fibrosis. A systematic literature review on the anti-fibrotic mechanisms of hepatoprotective plants was performed in PubMed, which yielded articles about twelve relevant plants. Many of these plants act via disruption of the transforming growth factor beta 1 signaling pathway, possibly through reduction in oxidative stress. This reduction could explain the inhibition of HSC activation and reduction in ECM deposition. Medicinal plants could be a source of anti-liver fibrosis compounds.

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Article number

4

Pages from-to (Number of pages)

Pages 27

Journal (Volume, Issue Number)

Chinese Medicine (Volume 9, Issue 12)

Publication milestones

  • Published - 01/01/2014

Publication status

Published - 01/01/2014

ISSN

1749-8546

Publication IDs

  • Scopus: 84923054566
  • PubMed: 25606051

Funding Details

Supported by: CONACYT for the PhD student grant. This work was partially funded by endowments from Instituto Tecnológico de Estudios Superiores de Monterrey (cat-134) and the Zambrano–Hellion Foundation.
FundersFunding numbers
Zambrano–Hellion Foundation
-
CONACYT
-
ITESM
cat-134