Intrahepatic upregulation of RhoA and Rho-kinase signalling contributes to increased hepatic vascular resistance in rats with secondary biliary cirrhosis

Gut. 2006 Sep;55(9):1296-305. doi: 10.1136/gut.2005.081059. Epub 2006 Feb 21.

Abstract

Background and aims: Portal hypertension in cirrhosis is mediated in part by increased intrahepatic resistance, reflecting an increased sensitivity of the hepatic microvasculature to vasoconstrictors. Activation of the RhoA/Rho-kinase pathway is essential for contraction of vascular smooth muscle. The aim of this study was to investigate RhoA/Rho-kinase mediated regulation of the intrahepatic vascular tone in cirrhotic rats.

Methods: Cirrhosis was induced by bile duct ligation (BDL). Hepatic RhoA and Rho-kinase expressions were studied by real time reverse transcription polymerase chain reaction and western blot analysis. Hepatic Rho-kinase activity in rat and human livers was assessed as phosphorylation of the Rho-kinase substrate moesin. The effect of the Rho-kinase inhibitor Y-27632 on hepatic perfusion pressure was measured in livers perfused at constant flow. The in vivo effect of intravenous application of Y-27632 was studied by haemodynamic measurements.

Results: Hepatic expressions of RhoA and Rho-kinase were increased at mRNA and protein level in BDL rats. Intrahepatic moesin phosphorylation was increased in livers from cirrhotic rats and patients with alcohol induced cirrhosis. Y-27632 reduced the basal perfusion pressure of in situ perfused livers in BDL rats but not in sham operated rats. Y-27632 reduced the sensitivity to methoxamine in isolated perfused livers in sham operated rats more than in BDL rats. In vivo, Y-27632 reduced portal pressure to a greater extent in BDL rats than in sham operated rats. Intrahepatic vascular resistance was decreased in response to bolus injection of Y-27632 in BDL rats but not in sham operated rats.

Conclusions: Upregulation of RhoA and Rho-kinase contributes to increased intrahepatic resistance in cirrhotic rats and to an increased sensitivity of cirrhotic livers to vasoconstrictors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Dose-Response Relationship, Drug
  • Hemodynamics / drug effects
  • Hypertension, Portal / etiology
  • Hypertension, Portal / physiopathology
  • Intracellular Signaling Peptides and Proteins
  • Liver / metabolism
  • Liver Circulation*
  • Liver Cirrhosis, Biliary / complications
  • Liver Cirrhosis, Biliary / metabolism*
  • Liver Cirrhosis, Biliary / physiopathology
  • Male
  • Methoxamine / pharmacology
  • Microfilament Proteins / metabolism
  • Phosphorylation
  • Protein Serine-Threonine Kinases / antagonists & inhibitors
  • Protein Serine-Threonine Kinases / biosynthesis*
  • Protein Serine-Threonine Kinases / genetics
  • Rats
  • Rats, Sprague-Dawley
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Signal Transduction
  • Up-Regulation
  • Vascular Resistance
  • Vasoconstrictor Agents / pharmacology
  • rho-Associated Kinases
  • rhoA GTP-Binding Protein / biosynthesis*
  • rhoA GTP-Binding Protein / genetics

Substances

  • Intracellular Signaling Peptides and Proteins
  • Microfilament Proteins
  • Vasoconstrictor Agents
  • moesin
  • Protein Serine-Threonine Kinases
  • rho-Associated Kinases
  • rhoA GTP-Binding Protein
  • Methoxamine