4.7 Article

Therapeutic effects of SMND-309, a new metabolite of salvianolic acid B, on experimental liver fibrosis

Journal

EUROPEAN JOURNAL OF PHARMACOLOGY
Volume 650, Issue 1, Pages 390-395

Publisher

ELSEVIER
DOI: 10.1016/j.ejphar.2010.10.019

Keywords

(2E) 2 {6 [(E) 2 carboxylvinyl]-2 3-dihydroxyphenyl} 3 (3 4-dihydroxyphenyl); propenoic acid (SMND 309); Liver fibrosis; Carbon tetrachloride; Lipid peroxidation; Transforming growth factor beta1 (TGF beta 1); Connective tissue growth factor (CTGF)

Funding

  1. Chinese Ministry of Education [209073]
  2. Education Department of Shandong Province [G08LE10]
  3. Shandong Province Science Foundation for Youths [BS2009SW012]

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(2E)-2-{6-[(E) 2-carboxylvinyl]-2 3-dihydroxyphenyl}-3-(3 4 dihydroxyphenyl) propenoic acid a novel compound designated SMND-309 is a new metabolite of salvianolic acid B The present study was carried out to investigate the effects of SMND 309 on experimental liver fibrosis in rats induced by subcutaneous injection of carbon tetrachloride and explore its possible mechanisms on the basis of biochemical histopathologic and immunohistochemical studies The results showed that intragastrical treatment with SMND 309 ameliorated liver function and decreased the elevation of serum hyaluronic acid laminin procollagen type III levels and hydroxyproline content in liver tissue It also decreased the elevation in the malondialdehyde level and restored the decrease in superoxide dismutase and glutathione peroxidase activities Upon histopathologic examination the SMND-309-treated rats reduced the liver damage and the liver fibrosis grade Moreover the results of immunohistochemical examination showed that SMND 309 powerfully down-regulated the expression of connective tissue growth factor (CTGF) rather than transforming growth factor-betal (TGF-beta 1) in serum and liver Meanwhile SMND-309 exhibits significantly higher potency compared with salvianolic acid B (Sal B) at the same dose The antifibrotic mechanisms of SMND 309 might be associated with its ability to suppress the expression of CTGF as well as scavenge lipid peroxidation products and increase endogenous antioxidant enzyme activity (C) 2010 Elsevier BV All rights reserved

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