Effects of L-ascorbic acid on lysyl oxidase in the formation of collagen cross-links

Biosci Biotechnol Biochem. 2002 Oct;66(10):2077-82. doi: 10.1271/bbb.66.2077.

Abstract

To clarify the role of L-ascorbic acid (AsA) in the formation of pyridinoline, we examined the effects of AsA in vitro using soluble collagen and partially purified lysyl oxidase from bovine aorta. The concentration of dehydrodihydroxylysinonorleucine decreased when AsA was added in the early stage of pyridinoline formation. However, when AsA was added in a later stage of pyridinoline formation, the concentration of pyridinoline was not affected. These findings indicated that AsA was involved in the initial enzymatic reaction in pyridinoline synthesis. We purified lysyl oxidase to confirm its association of AsA. AsA inhibited the enzyme activity. Erythorbic acid and 3,4-dihydroxybenzoate suppressed the enzyme activity as well as AsA did. The inhibition by AsA of the lysyl oxidase activity arose from characteristics of AsA structure. AsA might be important in the regulation of the oxidative reaction of lysine.

MeSH terms

  • Amino Acids / biosynthesis
  • Animals
  • Antioxidants / pharmacology*
  • Aorta, Thoracic / drug effects
  • Aorta, Thoracic / enzymology
  • Ascorbic Acid / pharmacology*
  • Cartilage / chemistry
  • Cattle
  • Collagen / chemistry*
  • Cross-Linking Reagents
  • Electrophoresis, Polyacrylamide Gel
  • Oxidation-Reduction
  • Protein-Lysine 6-Oxidase / chemistry
  • Protein-Lysine 6-Oxidase / metabolism*

Substances

  • Amino Acids
  • Antioxidants
  • Cross-Linking Reagents
  • pyridinoline
  • Collagen
  • Protein-Lysine 6-Oxidase
  • Ascorbic Acid