Literature DB >> 3237007

Formation of fluorescent substances from degradation products of methyl linoleate hydroperoxides with amino compound.

T Iio1, K Yoden.   

Abstract

The degradation products formed from methyl linoleate hydroperoxides by reaction with heme were fractionated by Sephadex LH-20 column chromatography and by reverse-phase high performance liquid chromatography, and the ability of each compound to form fluorescent substances through reaction with amino compound was compared. Maximum formation of fluorescent substances was obtained from monomeric degradation products with amino compound, but low molecular weight aldehydes such as hexanal, 2-hexenal and 2,4-decadienal, formed only a small amount of fluorescent substances. However, the major monomeric degradation products described previously, the hydroxy-, keto- and epoxy-derivatives, do not significantly contribute to the formation of fluorescent substances through reaction with amino compound. It was suggested that formation of fluorescent substances from lipid peroxides with amino compound may originate from a precursor present in monomeric degradation products formed from hydroperoxide of methyl linoleate during lipid peroxidation, and that low molecular weight aliphatic aldehydes are not involved in fluorescent substance formation. Moreover, the majority of TBA-reactive substances in secondary oxidation products prepared from autoxidized methyl linoleate are also unrelated to the formation of fluorescent substances through reaction with amino compound.

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Year:  1988        PMID: 3237007     DOI: 10.1007/bf02535654

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


  16 in total

1.  Studies of the fluorescent products of lipid oxidation in aqueous emulsion with glycine and on the surface of silica gel.

Authors:  H Shimasaki; O S Privett; I Hara
Journal:  J Am Oil Chem Soc       Date:  1977-03       Impact factor: 1.849

2.  Distribution of 14C after oral administration of [U-14C]labeled methyl linoleate hydroperoxides and their secondary oxidation products in rats.

Authors:  M Oarada; T Miyazawa; T Kaneda
Journal:  Lipids       Date:  1986-02       Impact factor: 1.880

3.  Fluorescent and cross-linked proteins of human erythrocyte ghosts formed by reaction with hydroperoxylinoleic acid, malonaldehyde and monofunctional aldehydes.

Authors:  M Beppu; K Murakami; K Kikugawa
Journal:  Chem Pharm Bull (Tokyo)       Date:  1986-02       Impact factor: 1.645

4.  Destruction of cytochrome P-450 by ethylene and other olefins.

Authors:  P R Ortiz de Montellano; B A Mico
Journal:  Mol Pharmacol       Date:  1980-07       Impact factor: 4.436

5.  Fluorescence formation from hydroperoxide of phosphatidylcholine with amino compound.

Authors:  T Iio; K Yoden
Journal:  Lipids       Date:  1988-01       Impact factor: 1.880

6.  The reaction of DNA with lipid oxidation products, metals and reducing agents.

Authors:  K Fujimoto; W E Neff; E N Frankel
Journal:  Biochim Biophys Acta       Date:  1984-08-15

7.  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

8.  Fluorescence formation from the interaction of DNA with lipid oxidation degradation products.

Authors:  E N Frankel; W E Neff; D D Brooks; K Fujimoto
Journal:  Biochim Biophys Acta       Date:  1987-06-23

9.  Possible involvement of the lipid-peroxidation product 4-hydroxynonenal in the formation of fluorescent chromolipids.

Authors:  H Esterbauer; E Koller; R G Slee; J F Koster
Journal:  Biochem J       Date:  1986-10-15       Impact factor: 3.857

10.  Conversion of linoleic acid hydroperoxide to hydroxy, keto, epoxyhydroxy, and trihydroxy fatty acids by hematin.

Authors:  T A Dix; L J Marnett
Journal:  J Biol Chem       Date:  1985-05-10       Impact factor: 5.157

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