Involvement of CPI-17 downregulation in the dysmotility of the colon from dextran sodium sulphate-induced experimental colitis in a mouse model

Neurogastroenterol Motil. 2007 Jun;19(6):504-14. doi: 10.1111/j.1365-2982.2007.00911.x.

Abstract

The mechanism of gastrointestinal dysmotility in inflammatory bowel disease has not been clarified. In this study, we examined the mechanism involved in the inflamed distal colon isolated from a mouse model of dextran sodium sulphate-induced ulcerative colitis (DSS-treated mouse). Although substance P-induced contraction was not changed, carbachol-induced contraction was reduced in the DSS-treated mouse colon. Pre-incubation with the NO synthase inhibitor N(G)-monomethyl-L-arginine (L-NMMA) or the cyclooxygenase inhibitor indomethacin did not reverse the carbachol-induced contraction in the DSS-treated mouse colon. In semi-quantitative reverse transcription-polymerase chain reaction experiments and Western blot analysis, muscarinic M3 receptor expressions were not changed. The Ca2+ -sensitization of contractile elements induced by carbachol with GTP or GTPgammaS was reduced in the beta-escin-permeabilized DSS-treated mouse colon. Although the expression of proteins such as rhoA, ROCK1, ROCK2 or MYPT1 in smooth muscles was not changed, the expression of CPI-17, the functional protein involved in smooth muscle Ca2+ -sensitization, was significantly decreased in the DSS-treated mouse colon. These results suggest that the suppression of carbachol-induced contraction in mice with colitis is attributable at least partially to the increased activity of myosin phosphatase following the downregulation of CPI-17.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anticoagulants / toxicity
  • Blotting, Western
  • Carbachol / pharmacology
  • Cholinergic Agonists / pharmacology
  • Colitis / chemically induced
  • Colitis / metabolism*
  • Colitis / pathology
  • Dextran Sulfate / toxicity
  • Disease Models, Animal
  • Down-Regulation
  • Enzyme Inhibitors / pharmacology
  • Female
  • Gastrointestinal Motility / drug effects
  • Gastrointestinal Motility / physiology*
  • Intracellular Signaling Peptides and Proteins
  • Mice
  • Mice, Inbred BALB C
  • Muscle Contraction / drug effects
  • Muscle Contraction / physiology
  • Muscle Proteins / drug effects
  • Muscle Proteins / metabolism*
  • Muscle, Smooth / drug effects
  • Muscle, Smooth / metabolism*
  • Phosphoproteins / drug effects
  • Phosphoproteins / metabolism*
  • Receptor, Muscarinic M3 / biosynthesis
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Anticoagulants
  • Cholinergic Agonists
  • Enzyme Inhibitors
  • Intracellular Signaling Peptides and Proteins
  • Muscle Proteins
  • Phosphoproteins
  • Ppp1r14a protein, mouse
  • Receptor, Muscarinic M3
  • Carbachol
  • Dextran Sulfate