Two distinct pathways of formation of 4-hydroxynonenal. Mechanisms of nonenzymatic transformation of the 9- and 13-hydroperoxides of linoleic acid to 4-hydroxyalkenals

J Biol Chem. 2001 Jun 15;276(24):20831-8. doi: 10.1074/jbc.M101821200. Epub 2001 Mar 19.

Abstract

The mechanism of formation of 4-hydroxy-2E-nonenal (4-HNE) has been a matter of debate since it was discovered as a major cytotoxic product of lipid peroxidation in 1980. Recent evidence points to 4-hydroperoxy-2E-nonenal (4-HPNE) as the immediate precursor of 4-HNE (Lee, S. H., and Blair, I. A. (2000) Chem. Res. Toxicol. 13, 698-702; Noordermeer, M. A., Feussner, I., Kolbe, A., Veldink, G. A., and Vliegenthart, J. F. G. (2000) Biochem. Biophys. Res. Commun. 277, 112-116), and a pathway via 9-hydroperoxylinoleic acid and 3Z-nonenal is recognized in plant extracts. Using the 9- and 13-hydroperoxides of linoleic acid as starting material, we find that two distinct mechanisms lead to the formation of 4-H(P)NE and the corresponding 4-hydro(pero)xyalkenal that retains the original carboxyl group (9-hydroperoxy-12-oxo-10E-dodecenoic acid). Chiral analysis revealed that 4-HPNE formed from 13S-hydroperoxy-9Z,11E-octadecadienoic acid (13S-HPODE) retains >90% S configuration, whereas it is nearly racemic from 9S-hydroperoxy-10E,12Z-octadecadienoic acid (9S-HPODE). 9-Hydroperoxy-12-oxo-10E-dodecenoic acid is >90% S when derived from 9S-HPODE and almost racemic from 13S-HPODE. Through analysis of intermediates and products, we provide evidence that (i) allylic hydrogen abstraction at C-8 of 13S-HPODE leads to a 10,13-dihydroperoxide that undergoes cleavage between C-9 and C-10 to give 4S-HPNE, whereas direct Hock cleavage of the 13S-HPODE gives 12-oxo-9Z-dodecenoic acid, which oxygenates to racemic 9-hydroperoxy-12-oxo-10E-dodecenoic acid; by contrast, (ii) 9S-HPODE cleaves directly to 3Z-nonenal as a precursor of racemic 4-HPNE, whereas allylic hydrogen abstraction at C-14 and oxygenation to a 9,12-dihydroperoxide leads to chiral 9S-hydroperoxy-12-oxo-10E-dodecenoic acid. Our results distinguish two major pathways to the formation of 4-HNE that should apply also to other fatty acid hydroperoxides. Slight ( approximately 10%) differences in the observed chiralities from those predicted in the above mechanisms suggest the existence of additional routes to the 4-hydroxyalkenals.

Publication types

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

MeSH terms

  • Aldehyde-Lyases / metabolism
  • Aldehydes / chemistry*
  • Chromatography, High Pressure Liquid
  • Cucurbitaceae / enzymology
  • Cytochrome P-450 Enzyme System / metabolism
  • Glycine max / enzymology
  • Kinetics
  • Linoleic Acids / chemistry*
  • Linoleic Acids / metabolism*
  • Lipid Peroxides / chemistry*
  • Lipid Peroxides / metabolism*
  • Lipoxygenase / metabolism
  • Recombinant Proteins / metabolism
  • Spectrophotometry, Ultraviolet
  • Stereoisomerism
  • Vitamin E / chemistry

Substances

  • Aldehydes
  • Linoleic Acids
  • Lipid Peroxides
  • Recombinant Proteins
  • Vitamin E
  • 13-hydroperoxy-9,11-octadecadienoic acid
  • 9-hydroperoxy-11,12-octadecadienoic acid
  • Cytochrome P-450 Enzyme System
  • Lipoxygenase
  • Aldehyde-Lyases
  • hydroperoxide lyase
  • 4-hydroxy-2-nonenal