[Can ulinastatin be an effective inhibitor of human polymorphonuclear granulocyte elastase under severe stressed state?]

Nihon Geka Gakkai Zasshi. 1993 May;94(5):449-55.
[Article in Japanese]

Abstract

The inhibitory effect of ulinastatin (UST), an intrinsic human trypsin inhibitor was investigated on the activity of polymorphonuclear granulocyte elastase (PMNE) with or without alpha 1-protease inhibitor (alpha 1-PI) using the in vitro models. The results of the dodecyl-sulfate-electrophoresis (SDS-PAGE), indicated that splitting-action of crude granulocyte enzyme solution on the plasma fibronectin was inhibited by concentration-dependent UST of an equivalent value for treatment of stressed state. The PMNE-UST complex was competitively replaced by PMNE-alpha 1-PI complex in vitro models of inflammatory focus and circulation, hence UST was weaker than alpha 1-PI in its binding-affinity for PMNE. The PMNE activity was directly inhibited by UST in the inflammatory focus and circulation with or without alpha 1-PI.

MeSH terms

  • Binding, Competitive
  • Dose-Response Relationship, Drug
  • Fibronectins / metabolism
  • Glycoproteins / pharmacology*
  • Glycoproteins / physiology
  • Humans
  • In Vitro Techniques
  • Inflammation / enzymology
  • Leukocyte Elastase
  • Pancreatic Elastase / antagonists & inhibitors
  • Pancreatic Elastase / metabolism*
  • Stress, Physiological / enzymology*
  • alpha 1-Antitrypsin / metabolism

Substances

  • Fibronectins
  • Glycoproteins
  • alpha 1-Antitrypsin
  • Pancreatic Elastase
  • Leukocyte Elastase
  • urinastatin