Literature DB >> 2120528

Gas chromatographic analysis of reactive carbonyl compounds formed from lipids upon UV-irradiation.

K J Dennis1, T Shibamoto.   

Abstract

Peroxidation of lipids produces carbonyl compounds; some of these, e.g., malonaldehyde and 4-hydroxynonenal, are genotoxic because of their reactivity with biological nucleophiles. Analysis of the reactive carbonyl compounds is often difficult. The methylhydrazine method developed for malonaldehyde analysis was applied to simultaneously measure the products formed from linoleic acid, linolenic acid, arachidonic acid, and squalene upon ultraviolet-irradiation (UV-irradiation). The photoreaction products, saturated monocarbonyl, alpha,beta-unsaturated carbonyls, and beta-dicarbonyls, were derivatized with methylhydrazine to give hydrazones, pyrazolines, and pyrazoles, respectively. The derivatives were analyzed by gas chromatography and gas chromatography-mass spectrometry. Lipid peroxidation products identified included formaldehyde, acetaldehyde, acrolein, malonaldehyde, n-hexanal, and 4-hydroxy-2-nonenal. Malonaldehyde levels formed upon 4 hr of irradiation were 0.06 micrograms/mg from squalene, 2.4 micrograms/mg from linolenic acid, and 5.7 micrograms/mg from arachidonic acid. Significant levels of acrolein (2.5 micrograms/mg) and 4-hydroxy-2-nonenal (0.17 micrograms/mg) were also produced from arachidonic acid upon 4 hr irradiation.

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Year:  1990        PMID: 2120528     DOI: 10.1007/bf02538089

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


  10 in total

1.  Gas chromatographic analysis of free and bound malonaldehyde in rat liver homogenates.

Authors:  T Ichinose; M G Miller; T Shibamoto
Journal:  Lipids       Date:  1989-10       Impact factor: 1.880

2.  Inactivation of ribonuclease and other enzymes by peroxidizing lipids and by malonaldehyde.

Authors:  K S Chio; A L Tappel
Journal:  Biochemistry       Date:  1969-07       Impact factor: 3.162

3.  Occurrence of 4-hydroxyalkenals in rat tissues determined as pentafluorobenzyl oxime derivatives by gas chromatography-mass spectrometry.

Authors:  F J van Kuijk; D W Thomas; R J Stephens; E A Dratz
Journal:  Biochem Biophys Res Commun       Date:  1986-08-29       Impact factor: 3.575

4.  Molecular requirements for the mutagenicity of malondialdehyde and related acroleins.

Authors:  A K Basu; L J Marnett
Journal:  Cancer Res       Date:  1984-07       Impact factor: 12.701

5.  Production of malonaldehyde from squalene, a major skin surface lipid, during UV-irradiation.

Authors:  K J Dennis; T Shibamoto
Journal:  Photochem Photobiol       Date:  1989-05       Impact factor: 3.421

6.  Analysis of free malondialdehyde in photoirradiated corn oil and beef fat via a pyrazole derivative.

Authors:  K Umano; K J Dennis; T Shibamoto
Journal:  Lipids       Date:  1988-08       Impact factor: 1.880

7.  Separation and characterization of the aldehydic products of lipid peroxidation stimulated by carbon tetrachloride or ADP-iron in isolated rat hepatocytes and rat liver microsomal suspensions.

Authors:  G Poli; M U Dianzani; K H Cheeseman; T F Slater; J Lang; H Esterbauer
Journal:  Biochem J       Date:  1985-04-15       Impact factor: 3.857

8.  Quantitative determination of the lipid peroxidation product 4-hydroxynonenal by high-performance liquid chromatography.

Authors:  J Lang; C Celotto; H Esterbauer
Journal:  Anal Biochem       Date:  1985-11-01       Impact factor: 3.365

9.  The chemistry of lipid peroxidation metabolites: crosslinking reactions of malondialdehyde.

Authors:  V Nair; C S Cooper; D E Vietti; G A Turner
Journal:  Lipids       Date:  1986-01       Impact factor: 1.880

10.  Naturally occurring carbonyl compounds are mutagens in Salmonella tester strain TA104.

Authors:  L J Marnett; H K Hurd; M C Hollstein; D E Levin; H Esterbauer; B N Ames
Journal:  Mutat Res       Date:  1985 Jan-Feb       Impact factor: 2.433

  10 in total
  3 in total

Review 1.  Acrolein-mediated injury in nervous system trauma and diseases.

Authors:  Riyi Shi; Todd Rickett; Wenjing Sun
Journal:  Mol Nutr Food Res       Date:  2011-08-08       Impact factor: 5.914

2.  NADPH-dependent reductases involved in the detoxification of reactive carbonyls in plants.

Authors:  Yasuo Yamauchi; Ayaka Hasegawa; Ai Taninaka; Masaharu Mizutani; Yukihiro Sugimoto
Journal:  J Biol Chem       Date:  2010-12-17       Impact factor: 5.157

3.  Formation of genotoxic dicarbonyl compounds in dietary oils upon oxidation.

Authors:  Kazutoshi Fujioka; Takayuki Shibamoto
Journal:  Lipids       Date:  2004-05       Impact factor: 1.880

  3 in total

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