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Tetrandrine induces apoptosis in hepatic stellate cells.

Abstract
We have previously reported that tetrandrine reduced hepatic stellate cell activation and collagen accumulation in liver fibrosis induced by biliary obstruction. In the present study, we examined the apoptosis-inducing effect of tetrandrine on activated hepatic stellate cells, as the therapeutic goal in hepatic fibrosis is to eliminate the activated hepatic stellate cells by apoptosis. We used rat hepatic stellate cells transformed by Simian virus 40 (T-HSC/Cl-6) to overcome the limitations inherent in studying primary cultures of hepatic stellate cells. Tetrandrine treatment at doses of 25 and 50 microg/ml for 12 h induced apoptosis as confirmed by DNA fragmentation and increased sub-G1 DNA content as detected by flow cytometric analysis. Tetrandrine also induced the activation of caspase-3 protease and subsequent proteolytic cleavage of poly(ADP-ribose) polymerase. In conclusion, our results demonstrate that tetrandrine induces apoptosis of T-HSC/Cl-6 cells, and these results should contribute to the development of new agents for the treatment of hepatic fibrosis.
AuthorsYu-Zhe Zhao, Ji-Young Kim, Eun-Jeon Park, Sung Hee Lee, Sun-Wook Woo, Geonil Ko, Dong Hwan Sohn
JournalPhytotherapy research : PTR (Phytother Res) Vol. 18 Issue 4 Pg. 306-9 (Apr 2004) ISSN: 0951-418X [Print] England
PMID15162366 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright 2004 John Wiley & Sons, Ltd.
Chemical References
  • Alkaloids
  • Benzylisoquinolines
  • Drugs, Chinese Herbal
  • tetrandrine
  • Poly(ADP-ribose) Polymerases
  • Caspases
Topics
  • Alkaloids (administration & dosage, pharmacology, therapeutic use)
  • Animals
  • Apoptosis (drug effects)
  • Benzylisoquinolines (administration & dosage, pharmacology, therapeutic use)
  • Caspases (metabolism)
  • Cells, Cultured (drug effects)
  • DNA Fragmentation
  • Dose-Response Relationship, Drug
  • Drugs, Chinese Herbal (administration & dosage, pharmacology, therapeutic use)
  • Flow Cytometry
  • Liver (cytology, drug effects, enzymology)
  • Liver Cirrhosis (drug therapy)
  • Phytotherapy
  • Poly(ADP-ribose) Polymerases (metabolism)
  • Rats
  • Rats, Sprague-Dawley
  • Stephania tetrandra

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