An oral endothelin-A receptor antagonist blocks collagen synthesis and deposition in advanced rat liver fibrosis

Gastroenterology. 2000 Jun;118(6):1169-78. doi: 10.1016/s0016-5085(00)70370-2.

Abstract

Background & aims: Endothelin 1 induces contraction, proliferation, and collagen synthesis of hepatic stellate cells in vitro, which may be mediated via the endothelin A receptor. It is unknown if specific blockade of the endothelin A receptor inhibits hepatic fibrosis in vivo.

Methods: Groups of 10-20 rats with bile duct occlusion were treated with the nonpeptide endothelin-A receptor antagonist LU 135252 at 80 mg. kg(-1). day(-1) from week 1-6 or from week 4-6, or with LU at 10 mg. kg(-1). day(-1) from week 1-6. Animals with bile duct occlusion alone and sham-operated rats without or with LU at 80 mg. kg(-1). day(-1) over 6 weeks served as controls. After 6 weeks, parameters of fibrogenesis were determined.

Results: LU treatment led to improved histology, paralleled by a dose-dependence up to 60% reduction of liver collagen, even when administered at an advanced fibrosis stage. This was accompanied by a decreased messenger RNA of hepatic procollagen alpha1(I) and tissue inhibitor of metalloproteinase 1, 2 major effectors of fibrosis, and of serum procollagen type III, a surrogate marker of liver fibrogenesis.

Conclusions: Selective endothelin-A receptor blockade can dramatically reduce collagen accumulation in rat secondary biliary fibrosis, a model refractory to most potential antifibrotic agents. Endothelin-A receptor antagonists are promising antifibrotic agents in chronic liver disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Alanine Transaminase / blood
  • Alkaline Phosphatase / blood
  • Animals
  • Ascites / drug therapy
  • Ascites / metabolism
  • Aspartate Aminotransferases / blood
  • Bilirubin / blood
  • Cholestasis / drug therapy
  • Cholestasis / metabolism
  • Cholestasis / pathology
  • Collagen / analysis
  • Collagen / biosynthesis*
  • DNA, Complementary
  • Disease Models, Animal
  • Endothelin Receptor Antagonists*
  • Endothelin-1 / analysis
  • Female
  • Hydroxyproline / analysis
  • Hypertension, Portal / drug therapy
  • Hypertension, Portal / metabolism
  • Hypertension, Portal / pathology
  • Jaundice / drug therapy
  • Jaundice / metabolism
  • Liver / drug effects
  • Liver / metabolism
  • Liver / pathology
  • Liver Cirrhosis, Experimental / drug therapy
  • Liver Cirrhosis, Experimental / metabolism*
  • Liver Cirrhosis, Experimental / pathology
  • Organ Size
  • Phenylpropionates / pharmacology*
  • Pyrimidines / pharmacology*
  • RNA, Messenger / analysis
  • Rats
  • Rats, Wistar
  • Receptor, Endothelin A
  • Receptor, Endothelin B
  • Receptors, Endothelin / analysis
  • Receptors, Endothelin / metabolism*
  • Tissue Inhibitor of Metalloproteinase-1 / genetics

Substances

  • DNA, Complementary
  • Endothelin Receptor Antagonists
  • Endothelin-1
  • Phenylpropionates
  • Pyrimidines
  • RNA, Messenger
  • Receptor, Endothelin A
  • Receptor, Endothelin B
  • Receptors, Endothelin
  • Tissue Inhibitor of Metalloproteinase-1
  • darusentan
  • Collagen
  • Aspartate Aminotransferases
  • Alanine Transaminase
  • Alkaline Phosphatase
  • Bilirubin
  • Hydroxyproline