The enzymatic defence against glycation in health, disease and therapeutics: a symposium to examine the concept

Biochem Soc Trans. 2003 Dec;31(Pt 6):1341-2. doi: 10.1042/bst0311341.

Abstract

Glycation of proteins, nucleotides and basic phospholipids by glucose, glyoxal, methylglyoxal, 3-deoxyglucosone and other saccharide derivatives is potentially damaging to the proteome and mutagenic. It is now recognized that there is an enzymatic defence against glycation--a group of enzymes that suppress the physiological levels of potent glycating agents and repair glycated proteins: glyoxalase I, aldehyde reductases and dehydrogenases, amadoriase and fructosamine 3-phosphokinase. The enzymatic defence against glycation influences morbidity and the efficiency of drug therapy in certain diseases. Improved understanding of the balance between glycation and the enzymatic anti-glycation defence will advance disease diagnosis and therapy.

Publication types

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

MeSH terms

  • Glucose / metabolism*
  • Humans
  • Therapeutics*

Substances

  • Glucose