Inhibition of human leukocyte elastase by chemically and naturally oversulfated galactosaminoglycans

Carbohydr Res. 1995 Oct 23;276(2):401-8. doi: 10.1016/0008-6215(95)00179-w.

Abstract

Several samples of oversulfated chondroitin and dermatan were obtained by chemical sulfation and by SAX-HPLC enrichment. The starting products and oversulfated products were tested as potential inhibitors of human leukocyte elastase, an enzyme hypothesized to be involved in the etiology of diseases such as emphysema, atherosclerosis, and rheumatoid arthritis. Chemical oversulfation (SO3H/COOH 1.6-3.2), preferentially occurring at C-6 of galactosamine residues, was found generally to increase the inhibitory power on elastase. Chemically oversulfated galactosaminoglycans thus have potential as therapeutic agents, considering that they produce non-significant effects on the hemocoagulative system. Two naturally oversulfated dermatans sulfate (SO3H/COOH ca. 1.2), mainly oversulfated at C-2 of iduronic acid residues, showed comparatively higher anticoagulant activity (in the HC-II mediated thrombin inhibition test).

MeSH terms

  • Animals
  • Blood Coagulation / drug effects
  • Carbohydrate Sequence
  • Cartilage / chemistry
  • Cattle
  • Chondroitin Sulfates / metabolism
  • Chondroitin Sulfates / pharmacology*
  • Dermatan Sulfate / metabolism
  • Dermatan Sulfate / pharmacology*
  • Enzyme Inhibitors / chemistry
  • Enzyme Inhibitors / pharmacology*
  • Humans
  • Leukocyte Elastase
  • Leukocytes / enzymology
  • Molecular Sequence Data
  • Molecular Structure
  • Pancreatic Elastase / antagonists & inhibitors*
  • Polysaccharides / metabolism
  • Polysaccharides / pharmacology*
  • Sharks
  • Sulfates / metabolism
  • Sulfur Oxides / metabolism

Substances

  • Enzyme Inhibitors
  • Polysaccharides
  • Sulfates
  • Sulfur Oxides
  • Dermatan Sulfate
  • Chondroitin Sulfates
  • galactosaminoglycan
  • Pancreatic Elastase
  • Leukocyte Elastase
  • sulfur trioxide