Literature DB >> 16459928

Synthesis of dihydroperoxides of linoleic and linolenic acids and studies on their transformation to 4-hydroperoxynonenal.

Claus Schneider1, William E Boeglin, Huiyong Yin, Donald F Ste, David L Hachey, Ned A Porter, Alan R Brash.   

Abstract

The cytotoxic aldehydes 4-hydroxynonenal, 4-hydroperoxynonenal (4-HPNE), and 4-oxononenal are formed during lipid peroxidation via oxidative transformation of the hydroxy or hydroperoxy precursor fatty acids, respectively. The mechanism of the carbon chain cleavage reaction leading to the aldehyde fragments is not known, but Hock-cleavage of a suitable dihydroperoxide derivative was implicated to account for the fragmentation [Schneider, C., Tallman, K.A., Porter, N.A., and Brash, A.R. (2001) 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. 275, 20831-20838]. Both 8,13- and 10,13-dihydroperoxyoctadecadienoic acids (diHPODE) could serve as precursors in a Hock-cleavage leading to 4-HPNE via two different pathways. Here, we synthesized diastereomeric 9,12-, 10,12-, and 10,13-diHPODE using singlet oxidation of linoleic acid. 8,13-Dihydroperoxyoctadecatrienoic acid was synthesized by vitamin E-controlled autoxidation of gamma-linolenic acid followed by reaction with soybean lipoxygenase. The transformation of these potential precursors to 4-HPNE was studied under conditions of autoxidation, hematin-, and acid-catalysis. In contrast to 9- or 13-HPODE, neither of the dihydroperoxides formed 4-HPNE on autoxidation (lipid film, 37 degrees C), regardless of whether the free acid or the methyl ester derivative was used. Acid treatment of 10,13-diHPODE led to the expected formation of 4-HPNE as a significant product, in accord with a Hock-type cleavage reaction. We conclude that, although the suppression of 4-H(P)NE formation from monohydroperoxides by alpha-tocopherol indicates peroxyl radical reactions in the major route of carbon chain cleavage, the dihydroperoxides previously implicated are not intermediates in the autoxidative transformation of monohydroperoxy fatty acids to 4-HPNE and related aldehydes.

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Year:  2005        PMID: 16459928     DOI: 10.1007/s11745-005-1480-3

Source DB:  PubMed          Journal:  Lipids        ISSN: 0024-4201            Impact factor:   1.880


  24 in total

1.  Autoxidation of methyl linoleate: identification of the bis-allylic 11-hydroperoxide.

Authors:  A R Brash
Journal:  Lipids       Date:  2000-09       Impact factor: 1.880

2.  Characterization of 4-oxo-2-nonenal as a novel product of lipid peroxidation.

Authors:  S H Lee; I A Blair
Journal:  Chem Res Toxicol       Date:  2000-08       Impact factor: 3.739

3.  Covalent binding of hydroxy-alkenals 4-HDDE, 4-HHE, and 4-HNE to ethanolamine phospholipid subclasses.

Authors:  Sandrine Bacot; Nathalie Bernoud-Hubac; Naima Baddas; Bernard Chantegrel; Christian Deshayes; Alain Doutheau; Michel Lagarde; Michel Guichardant
Journal:  J Lipid Res       Date:  2003-02-16       Impact factor: 5.922

4.  Induction of apoptosis in colorectal carcinoma cells treated with 4-hydroxy-2-nonenal and structurally related aldehydic products of lipid peroxidation.

Authors:  James D West; Chuan Ji; Stephen T Duncan; Venkataraman Amarnath; Claus Schneider; Carmelo J Rizzo; Alan R Brash; Lawrence J Marnett
Journal:  Chem Res Toxicol       Date:  2004-04       Impact factor: 3.739

5.  Linoleate hydroperoxides are cleaved heterolytically into aldehydes by a Lewis acid in aprotic solvent.

Authors:  H W Gardner; R D Plattner
Journal:  Lipids       Date:  1984-04       Impact factor: 1.880

6.  A novel family of atherogenic oxidized phospholipids promotes macrophage foam cell formation via the scavenger receptor CD36 and is enriched in atherosclerotic lesions.

Authors:  Eugene A Podrez; Eugenia Poliakov; Zhongzhou Shen; Renliang Zhang; Yijun Deng; Mingjiang Sun; Paula J Finton; Lian Shan; Maria Febbraio; David P Hajjar; Roy L Silverstein; Henry F Hoff; Robert G Salomon; Stanley L Hazen
Journal:  J Biol Chem       Date:  2002-07-26       Impact factor: 5.157

Review 7.  Chemistry and biochemistry of 4-hydroxynonenal, malonaldehyde and related aldehydes.

Authors:  H Esterbauer; R J Schaur; H Zollner
Journal:  Free Radic Biol Med       Date:  1991       Impact factor: 7.376

8.  Identification of 4-hydroxynonenal as a cytotoxic product originating from the peroxidation of liver microsomal lipids.

Authors:  A Benedetti; M Comporti; H Esterbauer
Journal:  Biochim Biophys Acta       Date:  1980-11-07

9.  Evidence for aldehydes bound to liver microsomal protein following CCl4 or BrCCl3 poisoning.

Authors:  A Benedetti; H Esterbauer; M Ferrali; R Fulceri; M Comporti
Journal:  Biochim Biophys Acta       Date:  1982-05-13

10.  Effect of alpha-tocopherol on the volatile thermal decomposition products of methyl linoleate hydroperoxides.

Authors:  E N Frankel; H W Gardner
Journal:  Lipids       Date:  1989-07       Impact factor: 1.880

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  15 in total

1.  Formation of 4-hydroxynonenal from cardiolipin oxidation: Intramolecular peroxyl radical addition and decomposition.

Authors:  Wei Liu; Ned A Porter; Claus Schneider; Alan R Brash; Huiyong Yin
Journal:  Free Radic Biol Med       Date:  2010-11-01       Impact factor: 7.376

2.  An (1)O2 route to γ-hydroxyalkenal phospholipids by vitamin E-induced fragmentation of hydroperoxydiene-derived endoperoxides.

Authors:  Xiaodong Gu; Wujuan Zhang; Jaewoo Choi; Wei Li; Xi Chen; James M Laird; Robert G Salomon
Journal:  Chem Res Toxicol       Date:  2011-05-31       Impact factor: 3.739

Review 3.  Lipid peroxidation in cell death.

Authors:  Michael M Gaschler; Brent R Stockwell
Journal:  Biochem Biophys Res Commun       Date:  2017-02-03       Impact factor: 3.575

4.  Vitamin C supplementation lowers urinary levels of 4-hydroperoxy-2-nonenal metabolites in humans.

Authors:  Heather C Kuiper; Richard S Bruno; Maret G Traber; Jan F Stevens
Journal:  Free Radic Biol Med       Date:  2011-01-12       Impact factor: 7.376

5.  4-Hydroperoxy-2-nonenal is not just an intermediate but a reactive molecule that covalently modifies proteins to generate unique intramolecular oxidation products.

Authors:  Yuuki Shimozu; Keita Hirano; Takahiro Shibata; Noriyuki Shibata; Koji Uchida
Journal:  J Biol Chem       Date:  2011-06-20       Impact factor: 5.157

6.  Alpha-tocopherol is ineffective in preventing the decomposition of preformed lipid peroxides and may promote the accumulation of toxic aldehydes: a potential explanation for the failure of antioxidants to affect human atherosclerosis.

Authors:  Achuthan Raghavamenon; Mahdi Garelnabi; Sainath Babu; Alex Aldrich; Dmitry Litvinov; Sampath Parthasarathy
Journal:  Antioxid Redox Signal       Date:  2009-06       Impact factor: 8.401

Review 7.  Routes to 4-hydroxynonenal: fundamental issues in the mechanisms of lipid peroxidation.

Authors:  Claus Schneider; Ned A Porter; Alan R Brash
Journal:  J Biol Chem       Date:  2008-02-19       Impact factor: 5.157

8.  Mercapturic acid conjugates of 4-hydroxy-2-nonenal and 4-oxo-2-nonenal metabolites are in vivo markers of oxidative stress.

Authors:  Heather C Kuiper; Cristobal L Miranda; John D Sowell; Jan F Stevens
Journal:  J Biol Chem       Date:  2008-04-27       Impact factor: 5.157

9.  Demonstration of HNE-related aldehyde formation via lipoxygenase-catalyzed synthesis of a bis-allylic dihydroperoxide intermediate.

Authors:  Jing Jin; Yuxiang Zheng; Alan R Brash
Journal:  Chem Res Toxicol       Date:  2013-05-23       Impact factor: 3.739

10.  An update on products and mechanisms of lipid peroxidation.

Authors:  Claus Schneider
Journal:  Mol Nutr Food Res       Date:  2009-03       Impact factor: 5.914

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