Evidence for ozone formation in human atherosclerotic arteries

Science. 2003 Nov 7;302(5647):1053-6. doi: 10.1126/science.1089525.

Abstract

Here, we report evidence for the production of ozone in human disease. Signature products unique to cholesterol ozonolysis are present within atherosclerotic tissue at the time of carotid endarterectomy, suggesting that ozone production occurred during lesion development. Furthermore, advanced atherosclerotic plaques generate ozone when the leukocytes within the diseased arteries are activated in vitro. The steroids produced by cholesterol ozonolysis cause effects that are thought to be critical to the pathogenesis of atherosclerosis, including cytotoxicity, lipid-loading in macrophages, and deformation of the apolipoprotein B-100 secondary structure. We propose the trivial designation "atheronals" for this previously unrecognized class of steroids.

Publication types

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

MeSH terms

  • Arteriosclerosis / metabolism*
  • Carotid Arteries / metabolism*
  • Cholestanes / blood
  • Cholestanes / metabolism*
  • Cholestanes / pharmacology
  • Cholesterol / metabolism*
  • Dimethyl Sulfoxide / pharmacology
  • Endarterectomy, Carotid
  • Foam Cells / drug effects
  • Foam Cells / physiology
  • Humans
  • Hydrazones / metabolism
  • Indigo Carmine / metabolism
  • Inflammation
  • Leukocytes / metabolism
  • Lipoproteins, LDL / metabolism
  • Lipoproteins, LDL / pharmacology
  • Norsteroids / blood
  • Norsteroids / metabolism*
  • Norsteroids / pharmacology
  • Oxidation-Reduction
  • Ozone / metabolism*
  • Singlet Oxygen / metabolism
  • Sterols / blood
  • Sterols / metabolism*
  • Sterols / pharmacology
  • Tetradecanoylphorbol Acetate / pharmacology

Substances

  • 5,6-secosterol
  • 5-hydroxy-6-formyl-7-norcholesterol
  • Cholestanes
  • Hydrazones
  • Lipoproteins, LDL
  • Norsteroids
  • Sterols
  • Singlet Oxygen
  • Ozone
  • Cholesterol
  • Indigo Carmine
  • Tetradecanoylphorbol Acetate
  • Dimethyl Sulfoxide