Literature DB >> 3398718

Relative inhibitory potencies of flavonoids on 12-lipoxygenase of fish gill.

R J Hsieh1, J B German, J E Kinsella.   

Abstract

The relative efficacy of 10 flavonoid compounds and some common antioxidants in inhibiting 12-lipoxygenase of fish gill was determined. Lipoxygenase activity was measured by oxygen consumption with polarography and formation of hydroxy fatty acid using thin layer chromatography with autoradiography. Generally, the inhibition of 12-lipoxygenase by flavonoids was noncompetitive. The lipoxygenase product pattern did not change in the presence of flavonoids. Fisetin (3,3',4',7-tetrahydroxyflavone) and quercetin (3,3',4',5,7-pentahydroxyflavone) were the most potent inhibitors of 12-lipoxygenase, with IC50's of 0.25 and 0.4 microM respectively. These were compared with IC50's values of 5,1000 microM for BHA (t-butylhydroxyanisole) and BHT (t-butylhydroxytoluene) respectively. Possible inhibitory mechanisms and relationships between flavonoid structure and inhibitory potencies are discussed.

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Year:  1988        PMID: 3398718     DOI: 10.1007/bf02537342

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


  17 in total

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8.  Inhibition of the formation of 5-hydroxy-6,8,11,14-eicosatetraenoic acid from arachidonic acid in polymorphonuclear leukocytes by various coumarins.

Authors:  Y Kimura; H Okuda; S Arichi; K Baba; M Kozawa
Journal:  Biochim Biophys Acta       Date:  1985-04-25

9.  Caffeic acid is a selective inhibitor for leukotriene biosynthesis.

Authors:  Y Koshihara; T Neichi; S Murota; A Lao; Y Fujimoto; T Tatsuno
Journal:  Biochim Biophys Acta       Date:  1984-01-17

10.  Hydroperoxide metabolism in trout gill tissue: effect of glutathione on lipoxygenase products generated from arachidonic acid and docosahexaenoic acid.

Authors:  J B German; J E Kinsella
Journal:  Biochim Biophys Acta       Date:  1986-12-05
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