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The effects of taurochenodeoxycholic acid in preventing pulmonary fibrosis in mice.

Abstract
The present study prepared the pulmonary fibrosis model in mice by using Bleomycin and carry out the investigations on the effects of taurochenodeoxycholic acid (TCDCA) in preventing pulmonary fibrosis in mice. Expression profiles of the bile acid receptors in the lung of mice FXRα and TGR5 were examined, and pulmonary coefficient, pathohistology as well as expression of TNF-α, MMP-2, MMP-9 and TIMP-2 in pulmonary fibrosis mice. The results showed that FXRα and TGR5 simultaneously expressed in the lung of the mice; TCDCA in dosages of 0.05 and 0.1g/kg can extremely significantly decrease the pulmonary coefficient in the model mice (P>0.01), TCDCA in a dosage of 0.2g/kg significantly decreased the pulmonary coefficient in the model mice (P<0.05); TCDCA in dosages of 0.05 and 0.1g/kg significantly reduce the pathological damages on their lungs; TCDCA can extremely significantly decrease the expression levels of TNF-α and TIMP-2 in pulmonary tissues in the pulmonary fibrosis mice (P>0.01), the expression level of MMP-9 extremely significantly increased (P>0.01), while it has no significant effects on MMP2. The results as mentioned above indicated that TCDCA had antagonistic actions on pulmonary fibrosis in mice.
AuthorsChuan Zhou, Youfei Shi, Jinlian Li, Wen Zhang, Yanmin Wang, Yan Liu, Jianzhu Liu
JournalPakistan journal of pharmaceutical sciences (Pak J Pharm Sci) Vol. 26 Issue 4 Pg. 761-5 (Jul 2013) ISSN: 1011-601X [Print] Pakistan
PMID23811455 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Gpbar1 protein, mouse
  • Receptors, G-Protein-Coupled
  • Tumor Necrosis Factor-alpha
  • Taurochenodeoxycholic Acid
  • Matrix Metalloproteinase 2
  • Mmp2 protein, mouse
  • Matrix Metalloproteinase 9
  • Mmp9 protein, mouse
Topics
  • Animals
  • Female
  • Lung (metabolism, pathology)
  • Male
  • Matrix Metalloproteinase 2 (genetics)
  • Matrix Metalloproteinase 9 (genetics)
  • Mice
  • Pulmonary Fibrosis (metabolism, pathology, prevention & control)
  • Receptors, G-Protein-Coupled (genetics)
  • Staining and Labeling
  • Taurochenodeoxycholic Acid (pharmacology, therapeutic use)
  • Tumor Necrosis Factor-alpha (genetics)

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