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Preventative effect of Astragalus flavescens on hepatic fibrosis in rats and its mechanism of action

The aim of this study was to investigate the preventative effect of Astragalus flavescens on hepatic fibrosis in rats and its mechanism of action. A total of 60 rats were randomly divided into normal control, model control, high-dose treatment and low-dose treatment groups, and a hepatic fibrosis mo...

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Autores principales: LI, RONG, DAI, GUANGRONG, ZHAO, MENGYUN, ZHANG, YONGHONG, HUI, LI, ZHANG, XUELI, JIN, BIN
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3797310/
https://www.ncbi.nlm.nih.gov/pubmed/24137287
http://dx.doi.org/10.3892/etm.2013.1232
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author LI, RONG
DAI, GUANGRONG
ZHAO, MENGYUN
ZHANG, YONGHONG
HUI, LI
ZHANG, XUELI
JIN, BIN
author_facet LI, RONG
DAI, GUANGRONG
ZHAO, MENGYUN
ZHANG, YONGHONG
HUI, LI
ZHANG, XUELI
JIN, BIN
author_sort LI, RONG
collection PubMed
description The aim of this study was to investigate the preventative effect of Astragalus flavescens on hepatic fibrosis in rats and its mechanism of action. A total of 60 rats were randomly divided into normal control, model control, high-dose treatment and low-dose treatment groups, and a hepatic fibrosis model was established. The high- and low-dose treatment groups were treated with 2 g/100 g and 0.5 g/100 g Astragalus flavescens, respectively, once a day. Eight weeks following the initiation of treatment, the liver specimens of the rats were stained and observed under a light microscope. Hepatic fibrosis indices, specifically, type III precollagen (PC III), type IV collagen (C IV), hyaluronic acid (HA) and laminin (LN), were detected. Furthermore, the expression and localization of the hepatic fibrosis-related factors transforming growth factor-β1 (TGF-β1), connective tissue growth factor (CTGF) and platelet-derived growth factor-BB (PDGF-BB) were determined. The serum levels of hepatic fibrosis indices, and the liver tissue levels of hepatic fibrosis-related factors and collagen surface density in the model control group and the high- and low-dose treatment groups were significantly higher compared with those of the normal control group (P<0.05). In addition, the values in the two treatment groups were significantly lower compared with those of the model control group (P<0.05). The present study demonstrated that Astragalus flavescens effectively prevents hepatic fibrosis in rats. A possible mechanism for this is that it may reduce the expression levels of TGF-β1, PDGF-BB and CTGF, thereby inhibiting the activation of hepatic stellate cells and specifically blocking the signal transduction pathway of hepatic fibrosis.
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spelling pubmed-37973102013-10-17 Preventative effect of Astragalus flavescens on hepatic fibrosis in rats and its mechanism of action LI, RONG DAI, GUANGRONG ZHAO, MENGYUN ZHANG, YONGHONG HUI, LI ZHANG, XUELI JIN, BIN Exp Ther Med Articles The aim of this study was to investigate the preventative effect of Astragalus flavescens on hepatic fibrosis in rats and its mechanism of action. A total of 60 rats were randomly divided into normal control, model control, high-dose treatment and low-dose treatment groups, and a hepatic fibrosis model was established. The high- and low-dose treatment groups were treated with 2 g/100 g and 0.5 g/100 g Astragalus flavescens, respectively, once a day. Eight weeks following the initiation of treatment, the liver specimens of the rats were stained and observed under a light microscope. Hepatic fibrosis indices, specifically, type III precollagen (PC III), type IV collagen (C IV), hyaluronic acid (HA) and laminin (LN), were detected. Furthermore, the expression and localization of the hepatic fibrosis-related factors transforming growth factor-β1 (TGF-β1), connective tissue growth factor (CTGF) and platelet-derived growth factor-BB (PDGF-BB) were determined. The serum levels of hepatic fibrosis indices, and the liver tissue levels of hepatic fibrosis-related factors and collagen surface density in the model control group and the high- and low-dose treatment groups were significantly higher compared with those of the normal control group (P<0.05). In addition, the values in the two treatment groups were significantly lower compared with those of the model control group (P<0.05). The present study demonstrated that Astragalus flavescens effectively prevents hepatic fibrosis in rats. A possible mechanism for this is that it may reduce the expression levels of TGF-β1, PDGF-BB and CTGF, thereby inhibiting the activation of hepatic stellate cells and specifically blocking the signal transduction pathway of hepatic fibrosis. D.A. Spandidos 2013-10 2013-07-23 /pmc/articles/PMC3797310/ /pubmed/24137287 http://dx.doi.org/10.3892/etm.2013.1232 Text en Copyright © 2013, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
LI, RONG
DAI, GUANGRONG
ZHAO, MENGYUN
ZHANG, YONGHONG
HUI, LI
ZHANG, XUELI
JIN, BIN
Preventative effect of Astragalus flavescens on hepatic fibrosis in rats and its mechanism of action
title Preventative effect of Astragalus flavescens on hepatic fibrosis in rats and its mechanism of action
title_full Preventative effect of Astragalus flavescens on hepatic fibrosis in rats and its mechanism of action
title_fullStr Preventative effect of Astragalus flavescens on hepatic fibrosis in rats and its mechanism of action
title_full_unstemmed Preventative effect of Astragalus flavescens on hepatic fibrosis in rats and its mechanism of action
title_short Preventative effect of Astragalus flavescens on hepatic fibrosis in rats and its mechanism of action
title_sort preventative effect of astragalus flavescens on hepatic fibrosis in rats and its mechanism of action
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3797310/
https://www.ncbi.nlm.nih.gov/pubmed/24137287
http://dx.doi.org/10.3892/etm.2013.1232
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