Effect of S-ethylisothiourea, a putative inhibitor of inducible nitric oxide synthase, on mouse skin vascular permeability

Jpn J Pharmacol. 1996 Mar;70(3):269-71. doi: 10.1254/jjp.70.269.

Abstract

By dye leakage in mouse skin, we evaluated the inhibition of proinflammatory stimuli-induced plasma extravasation by a putative inhibitor of inducible nitric oxide synthase, S-ethylisothiourea. A low dose of S-ethylisothiourea (5 micrograms/kg) mimicked aminoguanidine in inhibiting the plasma extravasation elicited by lipopolysaccharide but not by 5-hydroxytryptamine or platelet-activating factor. A higher dose of S-ethylisothiourea (10 micrograms/kg) inhibited the plasma extravasation induced by 5-hydroxytryptamine slightly; however, it increased the basal dye leakage. Thus, S-ethylisothiourea may be used as a relatively specific inhibitor for inducible nitric oxide synthase in vivo.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Capillary Permeability / drug effects*
  • Enzyme Inhibitors / pharmacology*
  • Isothiuronium / analogs & derivatives*
  • Isothiuronium / pharmacology
  • Lipopolysaccharides / pharmacology
  • Male
  • Mice
  • Nitric Oxide Synthase / antagonists & inhibitors*
  • Platelet Activating Factor / pharmacology
  • Salmonella typhimurium
  • Serotonin / pharmacology
  • Skin / blood supply*

Substances

  • Enzyme Inhibitors
  • Lipopolysaccharides
  • Platelet Activating Factor
  • Isothiuronium
  • etiron
  • Serotonin
  • Nitric Oxide Synthase