Protease-activated receptor 2-mediated vasodilatation in humans in vivo: role of nitric oxide and prostanoids

Circulation. 2003 Feb 25;107(7):954-9. doi: 10.1161/01.cir.0000050620.37260.75.

Abstract

Background: Systemic hypotension as a consequence of vascular dysfunction is a well-recognized and important feature of critical illness. Although serine protease activation has been implicated as a cause of vascular dysfunction in systemic inflammation, the mechanism is unknown. Recently, a class of receptors with an entirely novel mechanism of action, protease-activated receptors (PARs), has been identified that would explain the link between protease activation and systemic hypotension. Our aim was to test the hypothesis that in vivo activation of protease-activated receptor 2 (PAR-2) in humans would mediate vasodilatation.

Methods and results: For these first-in-human studies, an activating peptide for the human PAR-2 receptor was synthesized and administered to healthy volunteers. Using both the dorsal hand vein technique and forearm plethysmography, we studied the effects of PAR-2 activation in human blood vessels and investigated the mechanism of vasodilation. Activation of PAR-2 receptors in vivo dilated human blood vessels in a dose-dependent manner, and the effects were reduced by inhibition of both nitric oxide and prostanoid synthesis

Conclusions: These findings demonstrate that serine protease activity can cause human vasodilation and provide a possible explanation of why serine protease activation in critical illness is associated with vascular dysfunction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aspirin / pharmacology
  • Cyclooxygenase Inhibitors / pharmacology
  • Dose-Response Relationship, Drug
  • Enzyme Inhibitors / pharmacology
  • Female
  • Humans
  • Male
  • Nitric Oxide / physiology*
  • Nitric Oxide Synthase / antagonists & inhibitors
  • Oligopeptides / blood
  • Oligopeptides / pharmacology*
  • Prostaglandins / physiology*
  • Receptor, PAR-2
  • Receptors, Thrombin / physiology*
  • Vasodilation* / drug effects
  • omega-N-Methylarginine / pharmacology

Substances

  • Cyclooxygenase Inhibitors
  • Enzyme Inhibitors
  • Oligopeptides
  • Prostaglandins
  • Receptor, PAR-2
  • Receptors, Thrombin
  • seryl-leucyl-isoleucyl--glycyl-lysyl-valine
  • omega-N-Methylarginine
  • Nitric Oxide
  • Nitric Oxide Synthase
  • Aspirin