The involvement of Rho-associated kinases in agonist-dependent contractions of human maternal and placental arteries at term gestation

Am J Obstet Gynecol. 2005 Sep;193(3 Pt 1):815-24. doi: 10.1016/j.ajog.2005.02.076.

Abstract

Objective: The purpose of this study was to assess the involvement of rho kinase (ROK) in agonist-dependent contraction of omental, myometrial, and placental arteries of pregnant women at term.

Study design: Wire myography was used to assess if contractions of intact or alpha-toxin-permeabilized arteries obtained from women at elective cesarean section were influenced by the ROK inhibitor Y-27632.

Results: Western blotting indicated the presence of ROKalpha in each of the 3 tissue types. In intact human omental, myometrial, or placental arteries, Y-27632 dose-dependently reduced constrictions to the thromboxane-mimetic U46619. In permeabilized vessels, U46619 induced substantial Ca(2+)-sensitization of contraction that was inhibited by Y27632. The phosphatase inhibitor calyculin A induced a Ca(2+)sensitization of contraction similar to that of U46619 in permeabilized omental arteries that was unaffected by Y-27632, suggesting that ROK may signal via myosin phosphatase in these vessels.

Conclusion: These results are the first report of the involvement of ROK in the receptor-coupled constriction of intact and permeabilized arteries from pregnant women.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amides / pharmacology
  • Arteries
  • Blotting, Western
  • Electrophoresis, Polyacrylamide Gel
  • Female
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Marine Toxins
  • Muscle Relaxants, Central / pharmacology
  • Muscle, Smooth, Vascular / drug effects
  • Muscle, Smooth, Vascular / physiology
  • Myometrium / blood supply
  • Omentum / blood supply
  • Oxazoles / pharmacology
  • Phosphoprotein Phosphatases / antagonists & inhibitors
  • Placenta / blood supply
  • Pregnancy
  • Pregnancy Trimester, Third / physiology*
  • Protein Serine-Threonine Kinases / metabolism
  • Protein Serine-Threonine Kinases / physiology*
  • Pyridines / pharmacology
  • Vasoconstriction / drug effects
  • Vasoconstriction / physiology*
  • rho-Associated Kinases

Substances

  • Amides
  • Intracellular Signaling Peptides and Proteins
  • Marine Toxins
  • Muscle Relaxants, Central
  • Oxazoles
  • Pyridines
  • Y 27632
  • calyculin A
  • Protein Serine-Threonine Kinases
  • rho-Associated Kinases
  • Phosphoprotein Phosphatases