Inhibition of myosin phosphatase by upregulated rho-kinase plays a key role for coronary artery spasm in a porcine model with interleukin-1beta

Circulation. 2000 Mar 21;101(11):1319-23. doi: 10.1161/01.cir.101.11.1319.

Abstract

Background: We recently demonstrated that the Rho-kinase-mediated pathway plays an important role for coronary artery spasm in our porcine model with interleukin-1beta (IL-1beta). In this study, we examined whether or not Rho-kinase is upregulated at the spastic site and if so, how it induces vascular smooth muscle hypercontraction.

Methods and results: Segments of the left porcine coronary artery were chronically treated from the adventitia with IL-1beta-bound microbeads. Two weeks after the operation, as reported previously, intracoronary serotonin repeatedly induced coronary hypercontractions at the IL-1beta-treated site both in vivo and in vitro, which were markedly inhibited by Y-27632, one of the specific inhibitors of Rho-kinase. Reverse transcription-polymerase chain reaction analysis demonstrated that the expression of Rho-kinase mRNA was significantly increased in the spastic compared with the control segment. Western blot analysis showed that during the serotonin-induced contractions, the extent of phosphorylation of the myosin-binding subunit of myosin phosphatase (MBS), one of the major substrates of Rho-kinase, was significantly greater in the spastic than in the control segment and that the increase in MBS phosphorylations was also markedly inhibited by Y-27632. There was a highly significant correlation between the extent of MBS phosphorylations and that of contractions.

Conclusions: These results indicate that Rho-kinase is upregulated at the spastic site and plays a key role in inducing vascular smooth muscle hypercontraction by inhibiting myosin phosphatase through the phosphorylation of MBS in our porcine model.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Coronary Vasospasm / chemically induced*
  • Coronary Vasospasm / physiopathology*
  • Interleukin-1* / administration & dosage
  • Intracellular Signaling Peptides and Proteins
  • Isoenzymes / metabolism
  • Microspheres
  • Myosin-Light-Chain Phosphatase
  • Myosins / metabolism
  • Phosphoprotein Phosphatases / antagonists & inhibitors*
  • Phosphoprotein Phosphatases / metabolism
  • Phosphorylation
  • Protein Serine-Threonine Kinases / physiology*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Swine
  • Up-Regulation
  • rho-Associated Kinases

Substances

  • Interleukin-1
  • Intracellular Signaling Peptides and Proteins
  • Isoenzymes
  • Protein Serine-Threonine Kinases
  • rho-Associated Kinases
  • Phosphoprotein Phosphatases
  • Myosin-Light-Chain Phosphatase
  • Myosins