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Volumn 49, Issue 1, 2010, Pages 1-8

Trans-4-hydroxy-2-hexenal, a product of n-3 fatty acid peroxidation: Make some room HNE...

Author keywords

4 hydroxy 2 hexenal; 4 hydroxy 2 nonenal; 4 oxo 2 hexenal; Aldehydes; Docosahexaenoic acid; Lipid peroxidation; Oxidative damage; Polyunsaturated fatty acid

Indexed keywords

2 HEXENAL; 4 HYDROXY 2 HEXENAL; 4 HYDROXYNONENAL; DOCOSAHEXAENOIC ACID; ICOSAPENTAENOIC ACID; OMEGA 3 FATTY ACID; OMEGA 6 FATTY ACID; POLYUNSATURATED FATTY ACID; UNCLASSIFIED DRUG; 4-HYDROXY-2-HEXENAL; 4-OXO-(E)-2-HEXENAL; ALDEHYDE; FISH OIL;

EID: 77953026426     PISSN: 08915849     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.freeradbiomed.2010.03.015     Document Type: Review
Times cited : (155)

References (114)
  • 1
    • 32944470020 scopus 로고    scopus 로고
    • Protein modifications by 4-hydroxynonenal and 4-hydroxyhexenal in light-exposed rat retina
    • Tanito M., Elliott M.H., Kotake Y., Anderson R.E. Protein modifications by 4-hydroxynonenal and 4-hydroxyhexenal in light-exposed rat retina. Invest. Ophthalmol. Vis. Sci. 2005, 46:3859-3868.
    • (2005) Invest. Ophthalmol. Vis. Sci. , vol.46 , pp. 3859-3868
    • Tanito, M.1    Elliott, M.H.2    Kotake, Y.3    Anderson, R.E.4
  • 2
    • 73449134762 scopus 로고    scopus 로고
    • Ethanol withdrawal increases glutathione adducts of 4-hydroxy-2-hexenal but not 4-hydroxyl-2-nonenal in the rat cerebral cortex
    • Long E.K., Rosenberger T.A., Picklo M.J. Ethanol withdrawal increases glutathione adducts of 4-hydroxy-2-hexenal but not 4-hydroxyl-2-nonenal in the rat cerebral cortex. Free Radic. Biol. Med. 2010, 48:384-390.
    • (2010) Free Radic. Biol. Med. , vol.48 , pp. 384-390
    • Long, E.K.1    Rosenberger, T.A.2    Picklo, M.J.3
  • 4
    • 0021842533 scopus 로고
    • 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
    • Poli G., Dianzani M.U., Cheeseman K.H., Slater T.F., Lang J., Esterbauer H. 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. Biochem. J. 1985, 227:629-638.
    • (1985) Biochem. J. , vol.227 , pp. 629-638
    • Poli, G.1    Dianzani, M.U.2    Cheeseman, K.H.3    Slater, T.F.4    Lang, J.5    Esterbauer, H.6
  • 5
    • 29444461141 scopus 로고    scopus 로고
    • Synthesis of dihydroperoxides of linoleic and linolenic acids and studies on their transformation to 4-hydroperoxynonenal
    • Schneider C., Boeglin W.E., Yin H., Ste D.F., Hachey D.L., Porter N.A., Brash A.R. Synthesis of dihydroperoxides of linoleic and linolenic acids and studies on their transformation to 4-hydroperoxynonenal. Lipids 2005, 40:1155-1162.
    • (2005) Lipids , vol.40 , pp. 1155-1162
    • Schneider, C.1    Boeglin, W.E.2    Yin, H.3    Ste, D.F.4    Hachey, D.L.5    Porter, N.A.6    Brash, A.R.7
  • 6
    • 3242704996 scopus 로고    scopus 로고
    • Autoxidative transformation of chiral omega6 hydroxy linoleic and arachidonic acids to chiral 4-hydroxy-2e-nonenal
    • Schneider C., Porter N.A., Brash A.R. Autoxidative transformation of chiral omega6 hydroxy linoleic and arachidonic acids to chiral 4-hydroxy-2e-nonenal. Chem. Res. Toxicol. 2004, 17:937-941.
    • (2004) Chem. Res. Toxicol. , vol.17 , pp. 937-941
    • Schneider, C.1    Porter, N.A.2    Brash, A.R.3
  • 7
    • 0035877699 scopus 로고    scopus 로고
    • Two distinct pathways of formation of 4-hydroxynonenal. Mechanisms of nonenzymatic transformation of the 9- and 13-hydroperoxides of linoleic acid to 4-hydroxyalkenals
    • Schneider C., Tallman K.A., Porter N.A., Brash A.R. 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, 276:20831-20838.
    • (2001) J. Biol. Chem. , vol.276 , pp. 20831-20838
    • Schneider, C.1    Tallman, K.A.2    Porter, N.A.3    Brash, A.R.4
  • 8
    • 47049095632 scopus 로고    scopus 로고
    • Routes to 4-hydroxynonenal: Fundamental issues in the mechanisms of lipid peroxidation
    • Schneider C., Porter N.A., Brash A.R. Routes to 4-hydroxynonenal: Fundamental issues in the mechanisms of lipid peroxidation. J. Biol. Chem. 2008, 283:15539-15543.
    • (2008) J. Biol. Chem. , vol.283 , pp. 15539-15543
    • Schneider, C.1    Porter, N.A.2    Brash, A.R.3
  • 9
    • 0021154981 scopus 로고
    • Autooxidation of docosahexaenoic acid: Analysis of ten isomers of hydroxydocosahexaenoate
    • VanRollins M., Murphy R.C. Autooxidation of docosahexaenoic acid: Analysis of ten isomers of hydroxydocosahexaenoate. J. Lipid Res. 1984, 25:507-517.
    • (1984) J. Lipid Res. , vol.25 , pp. 507-517
    • VanRollins, M.1    Murphy, R.C.2
  • 10
    • 33846862209 scopus 로고    scopus 로고
    • Lipidomic analysis for lipid peroxidation-derived aldehydes using gas chromatography-mass spectrometry
    • Kawai Y., Takeda S., Terao J. Lipidomic analysis for lipid peroxidation-derived aldehydes using gas chromatography-mass spectrometry. Chem. Res. Toxicol. 2007, 20:99-107.
    • (2007) Chem. Res. Toxicol. , vol.20 , pp. 99-107
    • Kawai, Y.1    Takeda, S.2    Terao, J.3
  • 11
    • 0025099678 scopus 로고
    • 4-hydroxyhexenal: A lipid peroxidation product derived from oxidized docosahexaenoic acid
    • Van Kuijk F.J., Holte L.L., Dratz E.A. 4-hydroxyhexenal: A lipid peroxidation product derived from oxidized docosahexaenoic acid. Biochim. Biophys. Acta 1990, 1043:116-118.
    • (1990) Biochim. Biophys. Acta , vol.1043 , pp. 116-118
    • Van Kuijk, F.J.1    Holte, L.L.2    Dratz, E.A.3
  • 13
    • 48349108431 scopus 로고    scopus 로고
    • Structural characterization of alpha, beta-unsaturated aldehydes by gc/ms is dependent upon ionization method
    • Long E.K., Smoliakova I., Honzatko A., Picklo M.J. Structural characterization of alpha, beta-unsaturated aldehydes by gc/ms is dependent upon ionization method. Lipids 2008, 43:765-774.
    • (2008) Lipids , vol.43 , pp. 765-774
    • Long, E.K.1    Smoliakova, I.2    Honzatko, A.3    Picklo, M.J.4
  • 15
    • 0035874967 scopus 로고    scopus 로고
    • Vitamin c-induced decomposition of lipid hydroperoxides to endogenous genotoxins
    • Lee S.H., Oe T., Blair I.A. Vitamin c-induced decomposition of lipid hydroperoxides to endogenous genotoxins. Science 2001, 292:2083-2086.
    • (2001) Science , vol.292 , pp. 2083-2086
    • Lee, S.H.1    Oe, T.2    Blair, I.A.3
  • 16
    • 0033837032 scopus 로고    scopus 로고
    • Characterization of 4-oxo-2-nonenal as a novel product of lipid peroxidation
    • Lee S.H., Blair I.A. Characterization of 4-oxo-2-nonenal as a novel product of lipid peroxidation. Chem. Res. Toxicol. 2000, 13:698-702.
    • (2000) Chem. Res. Toxicol. , vol.13 , pp. 698-702
    • Lee, S.H.1    Blair, I.A.2
  • 17
    • 70849134064 scopus 로고    scopus 로고
    • Convergence of the 5-lox and cox-2 pathways. Heme-catalyzed cleavage of the 5s-hete-derived di-endoperoxide into aldehyde fragments
    • Griesser M., Boeglin W.E., Suzuki T., Schneider C. Convergence of the 5-lox and cox-2 pathways. Heme-catalyzed cleavage of the 5s-hete-derived di-endoperoxide into aldehyde fragments. J. Lipid Res. 2009, 50:2455-2462.
    • (2009) J. Lipid Res. , vol.50 , pp. 2455-2462
    • Griesser, M.1    Boeglin, W.E.2    Suzuki, T.3    Schneider, C.4
  • 18
    • 69249213880 scopus 로고    scopus 로고
    • A 4-oxo-2(e)-nonenal-derived glutathione adduct from 15-lipoxygenase-1-mediated oxidation of cytosolic and esterified arachidonic acid
    • Zhu P., Jian W., Blair I.A. A 4-oxo-2(e)-nonenal-derived glutathione adduct from 15-lipoxygenase-1-mediated oxidation of cytosolic and esterified arachidonic acid. Free Radic. Biol. Med. 2009, 47:953-961.
    • (2009) Free Radic. Biol. Med. , vol.47 , pp. 953-961
    • Zhu, P.1    Jian, W.2    Blair, I.A.3
  • 19
    • 0022342973 scopus 로고
    • Quantitative determination of the lipid peroxidation product 4-hydroxynonenal by high-performance liquid chromatography
    • Lang J., Celotto C., Esterbauer H. Quantitative determination of the lipid peroxidation product 4-hydroxynonenal by high-performance liquid chromatography. Anal. Biochem. 1985, 150:369-378.
    • (1985) Anal. Biochem. , vol.150 , pp. 369-378
    • Lang, J.1    Celotto, C.2    Esterbauer, H.3
  • 20
    • 0034810285 scopus 로고    scopus 로고
    • Enrichment of eggs with n-3 polyunsaturated fatty acids: Effects of vitamin e supplementation
    • Grune T., Kramer K., Hoppe P.P., Siems W. Enrichment of eggs with n-3 polyunsaturated fatty acids: Effects of vitamin e supplementation. Lipids 2001, 36:833-838.
    • (2001) Lipids , vol.36 , pp. 833-838
    • Grune, T.1    Kramer, K.2    Hoppe, P.P.3    Siems, W.4
  • 21
    • 0028890025 scopus 로고
    • Quantitative measurement of 4-hydroxyalkenals in oxidized low-density lipoprotein by gas chromatography-mass spectrometry
    • van Kuijk F.J., Siakotos A.N., Fong L.G., Stephens R.J., Thomas D.W. Quantitative measurement of 4-hydroxyalkenals in oxidized low-density lipoprotein by gas chromatography-mass spectrometry. Anal. Biochem. 1995, 224:420-424.
    • (1995) Anal. Biochem. , vol.224 , pp. 420-424
    • van Kuijk, F.J.1    Siakotos, A.N.2    Fong, L.G.3    Stephens, R.J.4    Thomas, D.W.5
  • 22
    • 0023510883 scopus 로고
    • Distribution of trans-4-hydroxy-2-hexenal and tandem mass spectrometric detection of its urinary mercapturic acid in the rat
    • Winter C.K., Segall H.J., Jones A.D. Distribution of trans-4-hydroxy-2-hexenal and tandem mass spectrometric detection of its urinary mercapturic acid in the rat. Drug Metab. Dispos. 1987, 15:608-612.
    • (1987) Drug Metab. Dispos. , vol.15 , pp. 608-612
    • Winter, C.K.1    Segall, H.J.2    Jones, A.D.3
  • 23
    • 0022410523 scopus 로고
    • Trans-4-hydroxy-2-hexenal: A reactive metabolite from the macrocyclic pyrrolizidine alkaloid senecionine
    • Segall H.J., Wilson D.W., Dallas J.L., Haddon W.F. Trans-4-hydroxy-2-hexenal: A reactive metabolite from the macrocyclic pyrrolizidine alkaloid senecionine. Science 1985, 229:472-475.
    • (1985) Science , vol.229 , pp. 472-475
    • Segall, H.J.1    Wilson, D.W.2    Dallas, J.L.3    Haddon, W.F.4
  • 24
    • 0028797410 scopus 로고
    • Mercapturic acid conjugates as urinary end metabolites of the lipid peroxidation product 4-hydroxy-2-nonenal in the rat
    • Alary J., Bravais F., Cravedi J.P., Debrauwer L., Rao D., Bories G. Mercapturic acid conjugates as urinary end metabolites of the lipid peroxidation product 4-hydroxy-2-nonenal in the rat. Chem. Res. Toxicol. 1995, 8:34-39.
    • (1995) Chem. Res. Toxicol. , vol.8 , pp. 34-39
    • Alary, J.1    Bravais, F.2    Cravedi, J.P.3    Debrauwer, L.4    Rao, D.5    Bories, G.6
  • 26
    • 0034599916 scopus 로고    scopus 로고
    • Metabolism of 4-hydroxynonenal, a cytotoxic product of lipid peroxidation, in rat precision-cut liver slices
    • Laurent A., Perdu-Durand E., Alary J., Debrauwer L., Cravedi J.P. Metabolism of 4-hydroxynonenal, a cytotoxic product of lipid peroxidation, in rat precision-cut liver slices. Toxicol. Lett. 2000, 114:203-214.
    • (2000) Toxicol. Lett. , vol.114 , pp. 203-214
    • Laurent, A.1    Perdu-Durand, E.2    Alary, J.3    Debrauwer, L.4    Cravedi, J.P.5
  • 27
    • 0028036292 scopus 로고
    • Detoxication of base propenals and other alpha, beta-unsaturated aldehyde products of radical reactions and lipid peroxidation by human glutathione transferases
    • Berhane K., Widersten M., Engstrom A., Kozarich J.W., Mannervik B. Detoxication of base propenals and other alpha, beta-unsaturated aldehyde products of radical reactions and lipid peroxidation by human glutathione transferases. Proc. Natl. Acad. Sci. U. S. A. 1994, 91:1480-1484.
    • (1994) Proc. Natl. Acad. Sci. U. S. A. , vol.91 , pp. 1480-1484
    • Berhane, K.1    Widersten, M.2    Engstrom, A.3    Kozarich, J.W.4    Mannervik, B.5
  • 28
    • 0032519517 scopus 로고    scopus 로고
    • Human glutathione transferase a4-4: An alpha class enzyme with high catalytic efficiency in the conjugation of 4-hydroxynonenal and other genotoxic products of lipid peroxidation
    • Hubatsch I., Ridderstrom M., Mannervik B. Human glutathione transferase a4-4: An alpha class enzyme with high catalytic efficiency in the conjugation of 4-hydroxynonenal and other genotoxic products of lipid peroxidation. Biochem. J. 1998, 330:175-179.
    • (1998) Biochem. J. , vol.330 , pp. 175-179
    • Hubatsch, I.1    Ridderstrom, M.2    Mannervik, B.3
  • 32
    • 0037627824 scopus 로고    scopus 로고
    • Oxidation of 4-hydroxy-2-nonenal by succinic semialdehyde dehydrogenase (aldh5a)
    • Murphy T.C., Amarnath V., Gibson K.M., Picklo M.J. Oxidation of 4-hydroxy-2-nonenal by succinic semialdehyde dehydrogenase (aldh5a). J. Neurochem. 2003, 86:298-305.
    • (2003) J. Neurochem. , vol.86 , pp. 298-305
    • Murphy, T.C.1    Amarnath, V.2    Gibson, K.M.3    Picklo, M.J.4
  • 33
    • 34447118905 scopus 로고    scopus 로고
    • Enantioselective oxidation of trans-4-hydroxy-2-nonenal is aldehyde dehydrogenase isozyme and mg2+ dependent
    • Brichac J., Ho K.K., Honzatko A., Wang R., Lu X., Weiner H., Picklo M.J. Enantioselective oxidation of trans-4-hydroxy-2-nonenal is aldehyde dehydrogenase isozyme and mg2+ dependent. Chem. Res. Toxicol. 2007, 20:887-895.
    • (2007) Chem. Res. Toxicol. , vol.20 , pp. 887-895
    • Brichac, J.1    Ho, K.K.2    Honzatko, A.3    Wang, R.4    Lu, X.5    Weiner, H.6    Picklo, M.J.7
  • 34
    • 0022640053 scopus 로고
    • Metabolism of the pyrrolizidine alkaloid metabolite trans-4-hydroxy-2-hexenal by mouse liver aldehyde dehydrogenases
    • Lame M.W., Segall H.J. Metabolism of the pyrrolizidine alkaloid metabolite trans-4-hydroxy-2-hexenal by mouse liver aldehyde dehydrogenases. Toxicol. Appl. Pharmacol. 1986, 82:94-103.
    • (1986) Toxicol. Appl. Pharmacol. , vol.82 , pp. 94-103
    • Lame, M.W.1    Segall, H.J.2
  • 35
    • 33846242976 scopus 로고    scopus 로고
    • Are 4-hydroxy-2(e)-nonenal derived mercapturic acids and (1)h nmr metabonomics potential biomarkers of chemically induced oxidative stress in the kidney?
    • Mally A., Amberg A., Hard G.C., Dekant W. Are 4-hydroxy-2(e)-nonenal derived mercapturic acids and (1)h nmr metabonomics potential biomarkers of chemically induced oxidative stress in the kidney?. Toxicology 2007, 230:244-255.
    • (2007) Toxicology , vol.230 , pp. 244-255
    • Mally, A.1    Amberg, A.2    Hard, G.C.3    Dekant, W.4
  • 36
    • 74149087999 scopus 로고    scopus 로고
    • Quantitation of mercapturic acid conjugates of 4-hydroxy-2-nonenal and 4-oxo-2-nonenal metabolites in a smoking cessation study
    • Kuiper H.C., Langsdorf B.L., Miranda C.L., Joss J., Jubert C., Mata J.E., Stevens J.F. Quantitation of mercapturic acid conjugates of 4-hydroxy-2-nonenal and 4-oxo-2-nonenal metabolites in a smoking cessation study. Free Radic. Biol. Med. 2010, 48:65-72.
    • (2010) Free Radic. Biol. Med. , vol.48 , pp. 65-72
    • Kuiper, H.C.1    Langsdorf, B.L.2    Miranda, C.L.3    Joss, J.4    Jubert, C.5    Mata, J.E.6    Stevens, J.F.7
  • 37
    • 47749105275 scopus 로고    scopus 로고
    • Mercapturic acid conjugates of 4-hydroxy-2-nonenal and 4-oxo-2-nonenal metabolites are in vivo markers of oxidative stress
    • Kuiper H.C., Miranda C.L., Sowell J.D., Stevens J.F. Mercapturic acid conjugates of 4-hydroxy-2-nonenal and 4-oxo-2-nonenal metabolites are in vivo markers of oxidative stress. J. Biol. Chem. 2008, 283:17131-17138.
    • (2008) J. Biol. Chem. , vol.283 , pp. 17131-17138
    • Kuiper, H.C.1    Miranda, C.L.2    Sowell, J.D.3    Stevens, J.F.4
  • 38
    • 0036852609 scopus 로고    scopus 로고
    • Covalent modification of amino acid nucleophiles by the lipid peroxidation products 4-hydroxy-2-nonenal and 4-oxo-2-nonenal
    • Doorn J.A., Petersen D.R. Covalent modification of amino acid nucleophiles by the lipid peroxidation products 4-hydroxy-2-nonenal and 4-oxo-2-nonenal. Chem. Res. Toxicol. 2002, 15:1445-1450.
    • (2002) Chem. Res. Toxicol. , vol.15 , pp. 1445-1450
    • Doorn, J.A.1    Petersen, D.R.2
  • 39
    • 0037327992 scopus 로고    scopus 로고
    • Covalent adduction of nucleophilic amino acids by 4-hydroxynonenal and 4-oxononenal
    • Doorn J.A., Petersen D.R. Covalent adduction of nucleophilic amino acids by 4-hydroxynonenal and 4-oxononenal. Chem. Biol. Interact. 2003, 143-144:93-100.
    • (2003) Chem. Biol. Interact. , pp. 93-100
    • Doorn, J.A.1    Petersen, D.R.2
  • 40
    • 0025814980 scopus 로고
    • Chemistry and biochemistry of 4-hydroxynonenal, malondialdehyde, and related aldehydes
    • Esterbauer H., Schaur R., Zollner H. Chemistry and biochemistry of 4-hydroxynonenal, malondialdehyde, and related aldehydes. Free Radic. Biol. Med. 1991, 11:81-128.
    • (1991) Free Radic. Biol. Med. , vol.11 , pp. 81-128
    • Esterbauer, H.1    Schaur, R.2    Zollner, H.3
  • 41
    • 70349492687 scopus 로고    scopus 로고
    • Molecular mechanisms of 4-hydroxy-2-nonenal and acrolein toxicity: Nucleophilic targets and adduct formation
    • LoPachin R.M., Gavin T., Petersen D.R., Barber D.S. Molecular mechanisms of 4-hydroxy-2-nonenal and acrolein toxicity: Nucleophilic targets and adduct formation. Chem. Res. Toxicol. 2009, 22:1499-1508.
    • (2009) Chem. Res. Toxicol. , vol.22 , pp. 1499-1508
    • LoPachin, R.M.1    Gavin, T.2    Petersen, D.R.3    Barber, D.S.4
  • 44
    • 0023009007 scopus 로고
    • Formation of cyclic adducts of deoxyguanosine with the aldehydes trans-4-hydroxy-2-hexenal and trans-4-hydroxy-2-nonenal in vitro
    • Winter C.K., Segall H.J., Haddon W.F. Formation of cyclic adducts of deoxyguanosine with the aldehydes trans-4-hydroxy-2-hexenal and trans-4-hydroxy-2-nonenal in vitro. Cancer Res. 1986, 46:5682-5686.
    • (1986) Cancer Res. , vol.46 , pp. 5682-5686
    • Winter, C.K.1    Segall, H.J.2    Haddon, W.F.3
  • 46
    • 0022340445 scopus 로고
    • In vivo covalent binding of trans-4-hydroxy-2-hexenal to rat liver macromolecules
    • Grasse L.D., Lame M.W., Segall H.J. In vivo covalent binding of trans-4-hydroxy-2-hexenal to rat liver macromolecules. Toxicol. Lett. 1985, 29:43-49.
    • (1985) Toxicol. Lett. , vol.29 , pp. 43-49
    • Grasse, L.D.1    Lame, M.W.2    Segall, H.J.3
  • 47
    • 0022537754 scopus 로고
    • Cytotoxicity, DNA fragmentation and sister-chromatid exchange in chinese hamster ovary cells exposed to the lipid peroxidation product 4-hydroxynonenal and homologous aldehydes
    • Brambilla G., Sciaba L., Faggin P., Maura A., Marinari U.M., Ferro M., Esterbauer H. Cytotoxicity, DNA fragmentation and sister-chromatid exchange in chinese hamster ovary cells exposed to the lipid peroxidation product 4-hydroxynonenal and homologous aldehydes. Mutat. Res. 1986, 171:169-176.
    • (1986) Mutat. Res. , vol.171 , pp. 169-176
    • Brambilla, G.1    Sciaba, L.2    Faggin, P.3    Maura, A.4    Marinari, U.M.5    Ferro, M.6    Esterbauer, H.7
  • 48
    • 0027504262 scopus 로고
    • Genotoxic properties of 4-hydroxyalkenals and analogous aldehydes
    • Eckl P.M., Ortner A., Esterbauer H. Genotoxic properties of 4-hydroxyalkenals and analogous aldehydes. Mutat. Res. 1993, 290:183-192.
    • (1993) Mutat. Res. , vol.290 , pp. 183-192
    • Eckl, P.M.1    Ortner, A.2    Esterbauer, H.3
  • 50
    • 67649739492 scopus 로고    scopus 로고
    • High levels of retinal membrane docosahexaenoic acid increase susceptibility to stress-induced degeneration
    • Tanito M., Brush R.S., Elliott M.H., Wicker L.D., Henry K.R., Anderson R.E. High levels of retinal membrane docosahexaenoic acid increase susceptibility to stress-induced degeneration. J. Lipid Res. 2009, 50:807-819.
    • (2009) J. Lipid Res. , vol.50 , pp. 807-819
    • Tanito, M.1    Brush, R.S.2    Elliott, M.H.3    Wicker, L.D.4    Henry, K.R.5    Anderson, R.E.6
  • 54
    • 67349279818 scopus 로고    scopus 로고
    • Proteomic identification of hne-bound proteins in early alzheimer disease: Insights into the role of lipid peroxidation in the progression of ad
    • Reed T.T., Pierce W.M., Markesbery W.R., Butterfield D.A. Proteomic identification of hne-bound proteins in early alzheimer disease: Insights into the role of lipid peroxidation in the progression of ad. Brain Res. 2009, 1274:66-76.
    • (2009) Brain Res. , vol.1274 , pp. 66-76
    • Reed, T.T.1    Pierce, W.M.2    Markesbery, W.R.3    Butterfield, D.A.4
  • 55
    • 40849120274 scopus 로고    scopus 로고
    • Redox proteomic identification of 4-hydroxy-2-nonenal-modified brain proteins in amnestic mild cognitive impairment: Insight into the role of lipid peroxidation in the progression and pathogenesis of alzheimer's disease
    • Reed T., Perluigi M., Sultana R., Pierce W.M., Klein J.B., Turner D.M., Coccia R., Markesbery W.R., Butterfield D.A. Redox proteomic identification of 4-hydroxy-2-nonenal-modified brain proteins in amnestic mild cognitive impairment: Insight into the role of lipid peroxidation in the progression and pathogenesis of alzheimer's disease. Neurobiol. Dis. 2008, 30:107-120.
    • (2008) Neurobiol. Dis. , vol.30 , pp. 107-120
    • Reed, T.1    Perluigi, M.2    Sultana, R.3    Pierce, W.M.4    Klein, J.B.5    Turner, D.M.6    Coccia, R.7    Markesbery, W.R.8    Butterfield, D.A.9
  • 56
    • 41649118986 scopus 로고    scopus 로고
    • Identification of protein targets of 4-hydroxynonenal using click chemistry for ex vivo biotinylation of azido and alkynyl derivatives
    • Vila A., Tallman K.A., Jacobs A.T., Liebler D.C., Porter N.A., Marnett L.J. Identification of protein targets of 4-hydroxynonenal using click chemistry for ex vivo biotinylation of azido and alkynyl derivatives. Chem. Res. Toxicol. 2008, 21:432-444.
    • (2008) Chem. Res. Toxicol. , vol.21 , pp. 432-444
    • Vila, A.1    Tallman, K.A.2    Jacobs, A.T.3    Liebler, D.C.4    Porter, N.A.5    Marnett, L.J.6
  • 57
    • 33751516438 scopus 로고    scopus 로고
    • Identification of 4-hydroxynonenal-modified retinal proteins induced by photooxidative stress prior to retinal degeneration
    • Tanito M., Haniu H., Elliott M.H., Singh A.K., Matsumoto H., Anderson R.E. Identification of 4-hydroxynonenal-modified retinal proteins induced by photooxidative stress prior to retinal degeneration. Free Radic. Biol. Med. 2006, 41:1847-1859.
    • (2006) Free Radic. Biol. Med. , vol.41 , pp. 1847-1859
    • Tanito, M.1    Haniu, H.2    Elliott, M.H.3    Singh, A.K.4    Matsumoto, H.5    Anderson, R.E.6
  • 59
    • 25644451257 scopus 로고    scopus 로고
    • Modification of heat shock protein 90 by 4-hydroxynonenal in a rat model of chronic alcoholic liver disease
    • Carbone D.L., Doorn J.A., Kiebler Z., Ickes B.R., Petersen D.R. Modification of heat shock protein 90 by 4-hydroxynonenal in a rat model of chronic alcoholic liver disease. J. Pharmacol. Exp. Ther. 2005, 315:8-15.
    • (2005) J. Pharmacol. Exp. Ther. , vol.315 , pp. 8-15
    • Carbone, D.L.1    Doorn, J.A.2    Kiebler, Z.3    Ickes, B.R.4    Petersen, D.R.5
  • 60
    • 23844442198 scopus 로고    scopus 로고
    • Cysteine modification by lipid peroxidation products inhibits protein disulfide isomerase
    • Carbone D.L., Doorn J.A., Kiebler Z., Petersen D.R. Cysteine modification by lipid peroxidation products inhibits protein disulfide isomerase. Chem. Res. Toxicol. 2005, 18:1324-1331.
    • (2005) Chem. Res. Toxicol. , vol.18 , pp. 1324-1331
    • Carbone, D.L.1    Doorn, J.A.2    Kiebler, Z.3    Petersen, D.R.4
  • 61
    • 34247361278 scopus 로고    scopus 로고
    • Carbonylation of adipose proteins in obesity and insulin resistance: Identification of adipocyte fatty acid-binding protein as a cellular target of 4-hydroxynonenal
    • Grimsrud P.A., Picklo M.J., Griffin T.J., Bernlohr D.A. Carbonylation of adipose proteins in obesity and insulin resistance: Identification of adipocyte fatty acid-binding protein as a cellular target of 4-hydroxynonenal. Mol. Cell. Proteomics 2007, 6:624-637.
    • (2007) Mol. Cell. Proteomics , vol.6 , pp. 624-637
    • Grimsrud, P.A.1    Picklo, M.J.2    Griffin, T.J.3    Bernlohr, D.A.4
  • 63
    • 16244389318 scopus 로고    scopus 로고
    • Reduced effect on apoptosis of 4-hydroxyhexenal and oxidized ldl enriched with n-3 fatty acids from postmenopausal women
    • Lee Y.S., Wander R.C. Reduced effect on apoptosis of 4-hydroxyhexenal and oxidized ldl enriched with n-3 fatty acids from postmenopausal women. J. Nutr. Biochem. 2005, 16:213-221.
    • (2005) J. Nutr. Biochem. , vol.16 , pp. 213-221
    • Lee, Y.S.1    Wander, R.C.2
  • 66
    • 0029866196 scopus 로고    scopus 로고
    • 4-hydroxyhexenal is a potent inducer of the mitochondrial permeability transition
    • Kristal B.S., Park B.K., Yu B.P. 4-hydroxyhexenal is a potent inducer of the mitochondrial permeability transition. J. Biol. Chem. 1996, 271:6033-6038.
    • (1996) J. Biol. Chem. , vol.271 , pp. 6033-6038
    • Kristal, B.S.1    Park, B.K.2    Yu, B.P.3
  • 67
    • 0030800033 scopus 로고    scopus 로고
    • Mitochondrial permeability transition in the central nervous system: Induction by calcium cycling-dependent and -independent pathways
    • Kristal B.S., Dubinsky J.M. Mitochondrial permeability transition in the central nervous system: Induction by calcium cycling-dependent and -independent pathways. J. Neurochem. 1997, 69:524-538.
    • (1997) J. Neurochem. , vol.69 , pp. 524-538
    • Kristal, B.S.1    Dubinsky, J.M.2
  • 69
    • 29644437160 scopus 로고    scopus 로고
    • 4-hydroxynonenal induces adaptive response and enhances pc12 cell tolerance primarily through induction of thioredoxin reductase 1 via activation of nrf2
    • Chen Z.H., Saito Y., Yoshida Y., Sekine A., Noguchi N., Niki E. 4-hydroxynonenal induces adaptive response and enhances pc12 cell tolerance primarily through induction of thioredoxin reductase 1 via activation of nrf2. J. Biol. Chem. 2005, 280:41921-41927.
    • (2005) J. Biol. Chem. , vol.280 , pp. 41921-41927
    • Chen, Z.H.1    Saito, Y.2    Yoshida, Y.3    Sekine, A.4    Noguchi, N.5    Niki, E.6
  • 71
    • 9144219652 scopus 로고    scopus 로고
    • A lipid peroxidation-derived inflammatory mediator: Identification of 4-hydroxy-2-nonenal as a potential inducer of cyclooxygenase-2 in macrophages
    • Kumagai T., Matsukawa N., Kaneko Y., Kusumi Y., Mitsumata M., Uchida K. A lipid peroxidation-derived inflammatory mediator: Identification of 4-hydroxy-2-nonenal as a potential inducer of cyclooxygenase-2 in macrophages. J. Biol. Chem. 2004, 279:48389-48396.
    • (2004) J. Biol. Chem. , vol.279 , pp. 48389-48396
    • Kumagai, T.1    Matsukawa, N.2    Kaneko, Y.3    Kusumi, Y.4    Mitsumata, M.5    Uchida, K.6
  • 72
    • 70249087960 scopus 로고    scopus 로고
    • The role of c-jun phosphorylation in epre activation of phase ii genes
    • Levy S., Jaiswal A.K., Forman H.J. The role of c-jun phosphorylation in epre activation of phase ii genes. Free Radic. Biol. Med. 2009, 47:1172-1179.
    • (2009) Free Radic. Biol. Med. , vol.47 , pp. 1172-1179
    • Levy, S.1    Jaiswal, A.K.2    Forman, H.J.3
  • 74
    • 33646372991 scopus 로고    scopus 로고
    • Reactive lipid species from cyclooxygenase-2 inactivate tumor suppressor lkb1/stk11: Cyclopentenone prostaglandins and 4-hydroxy-2-nonenal covalently modify and inhibit the amp-kinase kinase that modulates cellular energy homeostasis and protein translation
    • Wagner T.M., Mullally J.E., Fitzpatrick F.A. Reactive lipid species from cyclooxygenase-2 inactivate tumor suppressor lkb1/stk11: Cyclopentenone prostaglandins and 4-hydroxy-2-nonenal covalently modify and inhibit the amp-kinase kinase that modulates cellular energy homeostasis and protein translation. J. Biol. Chem. 2006, 281:2598-2604.
    • (2006) J. Biol. Chem. , vol.281 , pp. 2598-2604
    • Wagner, T.M.1    Mullally, J.E.2    Fitzpatrick, F.A.3
  • 75
    • 34248598495 scopus 로고    scopus 로고
    • The lipid peroxidation end-product 4-hne induces cox-2 expression through p38mapk activation in 3t3-l1 adipose cell
    • Zarrouki B., Soares A.F., Guichardant M., Lagarde M., Geloen A. The lipid peroxidation end-product 4-hne induces cox-2 expression through p38mapk activation in 3t3-l1 adipose cell. FEBS Lett. 2007, 581:2394-2400.
    • (2007) FEBS Lett. , vol.581 , pp. 2394-2400
    • Zarrouki, B.1    Soares, A.F.2    Guichardant, M.3    Lagarde, M.4    Geloen, A.5
  • 76
    • 33744970045 scopus 로고    scopus 로고
    • Gamma-glutamyl transpeptidase is induced by 4-hydroxynonenal via epre/nrf2 signaling in rat epithelial type ii cells
    • Zhang H., Liu H., Dickinson D.A., Liu R.M., Postlethwait E.M., Laperche Y., Forman H.J. Gamma-glutamyl transpeptidase is induced by 4-hydroxynonenal via epre/nrf2 signaling in rat epithelial type ii cells. Free Radic. Biol. Med. 2006, 40:1281-1292.
    • (2006) Free Radic. Biol. Med. , vol.40 , pp. 1281-1292
    • Zhang, H.1    Liu, H.2    Dickinson, D.A.3    Liu, R.M.4    Postlethwait, E.M.5    Laperche, Y.6    Forman, H.J.7
  • 77
    • 32044466295 scopus 로고    scopus 로고
    • 4-hydroxynonenal induces rat gamma-glutamyl transpeptidase through mitogen-activated protein kinase-mediated electrophile response element/nuclear factor erythroid 2-related factor 2 signaling
    • Zhang H., Liu H., Iles K.E., Liu R.M., Postlethwait E.M., Laperche Y., Forman H.J. 4-hydroxynonenal induces rat gamma-glutamyl transpeptidase through mitogen-activated protein kinase-mediated electrophile response element/nuclear factor erythroid 2-related factor 2 signaling. Am. J. Respir. Cell Mol. Biol. 2006, 34:174-181.
    • (2006) Am. J. Respir. Cell Mol. Biol. , vol.34 , pp. 174-181
    • Zhang, H.1    Liu, H.2    Iles, K.E.3    Liu, R.M.4    Postlethwait, E.M.5    Laperche, Y.6    Forman, H.J.7
  • 78
    • 2442693082 scopus 로고    scopus 로고
    • Nf-kappab activation mechanism of 4-hydroxyhexenal via nik/ikk and p38 mapk pathway
    • Je J.H., Lee J.Y., Jung K.J., Sung B., Go E.K., Yu B.P., Chung H.Y. Nf-kappab activation mechanism of 4-hydroxyhexenal via nik/ikk and p38 mapk pathway. FEBS Lett. 2004, 566:183-189.
    • (2004) FEBS Lett. , vol.566 , pp. 183-189
    • Je, J.H.1    Lee, J.Y.2    Jung, K.J.3    Sung, B.4    Go, E.K.5    Yu, B.P.6    Chung, H.Y.7
  • 79
    • 3142574551 scopus 로고    scopus 로고
    • Induction of endothelial inos by 4-hydroxyhexenal through nf-kappab activation
    • Lee J.Y., Je J.H., Jung K.J., Yu B.P., Chung H.Y. Induction of endothelial inos by 4-hydroxyhexenal through nf-kappab activation. Free Radic. Biol. Med. 2004, 37:539-548.
    • (2004) Free Radic. Biol. Med. , vol.37 , pp. 539-548
    • Lee, J.Y.1    Je, J.H.2    Jung, K.J.3    Yu, B.P.4    Chung, H.Y.5
  • 80
    • 1642396537 scopus 로고    scopus 로고
    • Role of nrf2 in the regulation of cd36 and stress protein expression in murine macrophages: Activation by oxidatively modified ldl and 4-hydroxynonenal
    • Ishii T., Itoh K., Ruiz E., Leake D.S., Unoki H., Yamamoto M., Mann G.E. Role of nrf2 in the regulation of cd36 and stress protein expression in murine macrophages: Activation by oxidatively modified ldl and 4-hydroxynonenal. Circ. Res. 2004, 94:609-616.
    • (2004) Circ. Res. , vol.94 , pp. 609-616
    • Ishii, T.1    Itoh, K.2    Ruiz, E.3    Leake, D.S.4    Unoki, H.5    Yamamoto, M.6    Mann, G.E.7
  • 81
    • 1642282736 scopus 로고    scopus 로고
    • Cellular mechanisms of redox cell signalling: Role of cysteine modification in controlling antioxidant defences in response to electrophilic lipid oxidation products
    • Levonen A.L., Landar A., Ramachandran A., Ceaser E.K., Dickinson D.A., Zanoni G., Morrow J.D., Darley-Usmar V.M. Cellular mechanisms of redox cell signalling: Role of cysteine modification in controlling antioxidant defences in response to electrophilic lipid oxidation products. Biochem. J. 2004, 378:373-382.
    • (2004) Biochem. J. , vol.378 , pp. 373-382
    • Levonen, A.L.1    Landar, A.2    Ramachandran, A.3    Ceaser, E.K.4    Dickinson, D.A.5    Zanoni, G.6    Morrow, J.D.7    Darley-Usmar, V.M.8
  • 82
    • 0344185338 scopus 로고    scopus 로고
    • Oxidized low-density lipoprotein and 15-deoxy-delta 12, 14-pgj2 increase mitochondrial complex i activity in endothelial cells
    • Ceaser E.K., Ramachandran A., Levonen A.L., Darley-Usmar V.M. Oxidized low-density lipoprotein and 15-deoxy-delta 12, 14-pgj2 increase mitochondrial complex i activity in endothelial cells. Am. J. Physiol. Heart Circ. Physiol. 2003, 285:H2298-H2308.
    • (2003) Am. J. Physiol. Heart Circ. Physiol. , vol.285
    • Ceaser, E.K.1    Ramachandran, A.2    Levonen, A.L.3    Darley-Usmar, V.M.4
  • 83
    • 33947517977 scopus 로고    scopus 로고
    • Proteasome inhibition induces glutathione synthesis and protects cells from oxidative stress: Relevance to parkinson disease
    • Yamamoto N., Sawada H., Izumi Y., Kume T., Katsuki H., Shimohama S., Akaike A. Proteasome inhibition induces glutathione synthesis and protects cells from oxidative stress: Relevance to parkinson disease. J. Biol. Chem. 2007, 282:4364-4372.
    • (2007) J. Biol. Chem. , vol.282 , pp. 4364-4372
    • Yamamoto, N.1    Sawada, H.2    Izumi, Y.3    Kume, T.4    Katsuki, H.5    Shimohama, S.6    Akaike, A.7
  • 84
    • 33344469643 scopus 로고    scopus 로고
    • Oxidative and electrophilic stresses activate nrf2 through inhibition of ubiquitination activity of keap1
    • Kobayashi A., Kang M.I., Watai Y., Tong K.I., Shibata T., Uchida K., Yamamoto M. Oxidative and electrophilic stresses activate nrf2 through inhibition of ubiquitination activity of keap1. Mol. Cell. Biol. 2006, 26:221-229.
    • (2006) Mol. Cell. Biol. , vol.26 , pp. 221-229
    • Kobayashi, A.1    Kang, M.I.2    Watai, Y.3    Tong, K.I.4    Shibata, T.5    Uchida, K.6    Yamamoto, M.7
  • 86
    • 1942520367 scopus 로고    scopus 로고
    • Nrf2 signaling in coordinated activation of antioxidant gene expression
    • Jaiswal A.K. Nrf2 signaling in coordinated activation of antioxidant gene expression. Free Radic. Biol. Med. 2004, 36:1199-1207.
    • (2004) Free Radic. Biol. Med. , vol.36 , pp. 1199-1207
    • Jaiswal, A.K.1
  • 87
    • 67649402187 scopus 로고    scopus 로고
    • The nrf2-antioxidant response element signaling pathway and its activation by oxidative stress
    • Nguyen T., Nioi P., Pickett C.B. The nrf2-antioxidant response element signaling pathway and its activation by oxidative stress. J. Biol. Chem. 2009, 284:13291-13295.
    • (2009) J. Biol. Chem. , vol.284 , pp. 13291-13295
    • Nguyen, T.1    Nioi, P.2    Pickett, C.B.3
  • 88
    • 3142570440 scopus 로고    scopus 로고
    • The pathways and molecular mechanisms regulating nrf2 activation in response to chemical stress
    • Nguyen T., Yang C.S., Pickett C.B. The pathways and molecular mechanisms regulating nrf2 activation in response to chemical stress. Free Radic. Biol. Med. 2004, 37:433-441.
    • (2004) Free Radic. Biol. Med. , vol.37 , pp. 433-441
    • Nguyen, T.1    Yang, C.S.2    Pickett, C.B.3
  • 90
    • 13844298275 scopus 로고    scopus 로고
    • The effect of ethanol-induced cyp2e1 on proteasome activity: The role of 4-hydroxynonenal
    • Bardag-Gorce F., Li J., French B.A., French S.W. The effect of ethanol-induced cyp2e1 on proteasome activity: The role of 4-hydroxynonenal. Exp. Mol. Pathol. 2005, 78:109-115.
    • (2005) Exp. Mol. Pathol. , vol.78 , pp. 109-115
    • Bardag-Gorce, F.1    Li, J.2    French, B.A.3    French, S.W.4
  • 91
    • 10044294918 scopus 로고    scopus 로고
    • Catalytic site-specific inhibition of the 20s proteasome by 4-hydroxynonenal
    • Ferrington D.A., Kapphahn R.J. Catalytic site-specific inhibition of the 20s proteasome by 4-hydroxynonenal. FEBS Lett. 2004, 578:217-223.
    • (2004) FEBS Lett. , vol.578 , pp. 217-223
    • Ferrington, D.A.1    Kapphahn, R.J.2
  • 92
    • 0025193490 scopus 로고
    • Effect of 4-hydroxylalkenals on hepatic phosphatidylinositol-4, 5-bisphosphate-phospholipase c
    • Rossi M.A., Fidale F., Garramone A., Esterbauer H., Dianzani M.U. Effect of 4-hydroxylalkenals on hepatic phosphatidylinositol-4, 5-bisphosphate-phospholipase c. Biochem. Pharmacol. 1990, 39:1715-1719.
    • (1990) Biochem. Pharmacol. , vol.39 , pp. 1715-1719
    • Rossi, M.A.1    Fidale, F.2    Garramone, A.3    Esterbauer, H.4    Dianzani, M.U.5
  • 93
    • 3042695161 scopus 로고    scopus 로고
    • 4-hydroxy-trans-2-nonenoic acid is a gamma-hydroxybutyrate receptor ligand in the cerebral cortex and hippocampus
    • Murphy T.C., Poppe C., Porter J.E., Montine T.J., Picklo M.J. 4-hydroxy-trans-2-nonenoic acid is a gamma-hydroxybutyrate receptor ligand in the cerebral cortex and hippocampus. J. Neurochem. 2004, 89:1462-1470.
    • (2004) J. Neurochem. , vol.89 , pp. 1462-1470
    • Murphy, T.C.1    Poppe, C.2    Porter, J.E.3    Montine, T.J.4    Picklo, M.J.5
  • 94
    • 33745892100 scopus 로고    scopus 로고
    • Mitogenic responses of vascular smooth muscle cells to lipid peroxidation-derived aldehyde 4-hydroxy-trans-2-nonenal (hne): Role of aldose reductase-catalyzed reduction of the hne-glutathione conjugates in regulating cell growth
    • Ramana K.V., Bhatnagar A., Srivastava S., Yadav U.C., Awasthi S., Awasthi Y.C., Srivastava S.K. Mitogenic responses of vascular smooth muscle cells to lipid peroxidation-derived aldehyde 4-hydroxy-trans-2-nonenal (hne): Role of aldose reductase-catalyzed reduction of the hne-glutathione conjugates in regulating cell growth. J. Biol. Chem. 2006, 281:17652-17660.
    • (2006) J. Biol. Chem. , vol.281 , pp. 17652-17660
    • Ramana, K.V.1    Bhatnagar, A.2    Srivastava, S.3    Yadav, U.C.4    Awasthi, S.5    Awasthi, Y.C.6    Srivastava, S.K.7
  • 95
    • 70149123025 scopus 로고    scopus 로고
    • Resolvin d1 controls inflammation initiated by glutathione-lipid conjugates formed during oxidative stress
    • Spite M., Summers L., Porter T.F., Srivastava S., Bhatnagar A., Serhan C.N. Resolvin d1 controls inflammation initiated by glutathione-lipid conjugates formed during oxidative stress. Br. J. Pharmacol. 2009, 158:1062-1073.
    • (2009) Br. J. Pharmacol. , vol.158 , pp. 1062-1073
    • Spite, M.1    Summers, L.2    Porter, T.F.3    Srivastava, S.4    Bhatnagar, A.5    Serhan, C.N.6
  • 96
    • 77953023671 scopus 로고    scopus 로고
    • Inflammatory neurodegeneration and mechanisms of microglial killing of neurons
    • Mol. Neurobiol. in press
    • Brown, G. C.; Neher, J. J. Inflammatory neurodegeneration and mechanisms of microglial killing of neurons. Mol. Neurobiol. in press.
    • Brown, G.C.1    Neher, J.J.2
  • 97
    • 77953023629 scopus 로고    scopus 로고
    • Microglia activation and antiinflammatory regulation in alzheimer's disease
    • Mol. Neurobiol. in press
    • Lue, L. F.; Kuo, Y. M.; Beach, T.; Walker, D. G. Microglia activation and antiinflammatory regulation in alzheimer's disease. Mol. Neurobiol. in press.
    • Lue, L.F.1    Kuo, Y.M.2    Beach, T.3    Walker, D.G.4
  • 99
    • 0037181320 scopus 로고    scopus 로고
    • Oxidative stability of fish and algae oils containing long-chain polyunsaturated fatty acids in bulk and in oil-in-water emulsions
    • Frankel E.N., Satue-Gracia T., Meyer A.S., German J.B. Oxidative stability of fish and algae oils containing long-chain polyunsaturated fatty acids in bulk and in oil-in-water emulsions. J. Agric. Food Chem. 2002, 50:2094-2099.
    • (2002) J. Agric. Food Chem. , vol.50 , pp. 2094-2099
    • Frankel, E.N.1    Satue-Gracia, T.2    Meyer, A.S.3    German, J.B.4
  • 100
    • 33845901002 scopus 로고    scopus 로고
    • Effects of nacl on 4-hydroxy-2-hexenal formation in yellowtail meat stored at 0 degrees c
    • Munasinghe D.M., Kawahara S., Sakai T. Effects of nacl on 4-hydroxy-2-hexenal formation in yellowtail meat stored at 0 degrees c. Biosci. Biotechnol. Biochem. 2006, 70:3036-3038.
    • (2006) Biosci. Biotechnol. Biochem. , vol.70 , pp. 3036-3038
    • Munasinghe, D.M.1    Kawahara, S.2    Sakai, T.3
  • 101
    • 75049085322 scopus 로고    scopus 로고
    • Subgram daily supplementation with docosahexaenoic acid protects low-density lipoproteins from oxidation in healthy men
    • Calzada C., Colas R., Guillot N., Guichardant M., Laville M., Vericel E., Lagarde M. Subgram daily supplementation with docosahexaenoic acid protects low-density lipoproteins from oxidation in healthy men. Atherosclerosis 2010, 208:467-472.
    • (2010) Atherosclerosis , vol.208 , pp. 467-472
    • Calzada, C.1    Colas, R.2    Guillot, N.3    Guichardant, M.4    Laville, M.5    Vericel, E.6    Lagarde, M.7
  • 102
    • 57549111041 scopus 로고    scopus 로고
    • Oxidation products of polyunsaturated fatty acids in infant formulas compared to human milk-a preliminary study
    • Michalski M.C., Calzada C., Makino A., Michaud S., Guichardant M. Oxidation products of polyunsaturated fatty acids in infant formulas compared to human milk-a preliminary study. Mol. Nutr. Food Res. 2008, 52:1478-1485.
    • (2008) Mol. Nutr. Food Res. , vol.52 , pp. 1478-1485
    • Michalski, M.C.1    Calzada, C.2    Makino, A.3    Michaud, S.4    Guichardant, M.5
  • 103
    • 35248888920 scopus 로고    scopus 로고
    • 4-hydroxy-2-alkenals in polyunsaturated fatty acids-fortified infant formulas and other commercial food products
    • Surh J., Lee S., Kwon H. 4-hydroxy-2-alkenals in polyunsaturated fatty acids-fortified infant formulas and other commercial food products. Food Addit. Contam. 2007, 24:1209-1218.
    • (2007) Food Addit. Contam. , vol.24 , pp. 1209-1218
    • Surh, J.1    Lee, S.2    Kwon, H.3
  • 104
    • 47849083192 scopus 로고    scopus 로고
    • 4-oxo-2-hexenal, a mutagen formed by omega-3 fat peroxidation: Occurrence, detection and adduct formation
    • Kasai H., Kawai K. 4-oxo-2-hexenal, a mutagen formed by omega-3 fat peroxidation: Occurrence, detection and adduct formation. Mutat. Res. 2008, 659:56-59.
    • (2008) Mutat. Res. , vol.659 , pp. 56-59
    • Kasai, H.1    Kawai, K.2
  • 106
    • 32344436279 scopus 로고    scopus 로고
    • Detection of 4-oxo-2-hexenal, a novel mutagenic product of lipid peroxidation, in human diet and cooking vapor
    • Kawai K., Matsuno K., Kasai H. Detection of 4-oxo-2-hexenal, a novel mutagenic product of lipid peroxidation, in human diet and cooking vapor. Mutat. Res. 2006, 603:186-192.
    • (2006) Mutat. Res. , vol.603 , pp. 186-192
    • Kawai, K.1    Matsuno, K.2    Kasai, H.3
  • 107
    • 20544476967 scopus 로고    scopus 로고
    • Attraction of male european tarnished plant bug, lygus rugulipennis to components of the female sex pheromone in the field
    • Innocenzi P.J., Hall D., Cross J.V., Hesketh H. Attraction of male european tarnished plant bug, lygus rugulipennis to components of the female sex pheromone in the field. J. Chem. Ecol. 2005, 31:1401-1413.
    • (2005) J. Chem. Ecol. , vol.31 , pp. 1401-1413
    • Innocenzi, P.J.1    Hall, D.2    Cross, J.V.3    Hesketh, H.4
  • 108
    • 4644252002 scopus 로고    scopus 로고
    • Investigation of long-range female sex pheromone of the european tarnished plant bug, lygus rugulipennis: Chemical, electrophysiological, and field studies
    • Innocenzi P.J., Hall D.R., Cross J.V., Masuh H., Phythian S.J., Chittamaru S., Guarino S. Investigation of long-range female sex pheromone of the european tarnished plant bug, lygus rugulipennis: Chemical, electrophysiological, and field studies. J. Chem. Ecol. 2004, 30:1509-1529.
    • (2004) J. Chem. Ecol. , vol.30 , pp. 1509-1529
    • Innocenzi, P.J.1    Hall, D.R.2    Cross, J.V.3    Masuh, H.4    Phythian, S.J.5    Chittamaru, S.6    Guarino, S.7
  • 109
    • 0035014357 scopus 로고    scopus 로고
    • Defensive chemistry of an aposematic bug, pachycoris stallii uhler and volatile compounds of its host plant croton californicus muell.-arg
    • Williams L., Evans P.E., Bowers W.S. Defensive chemistry of an aposematic bug, pachycoris stallii uhler and volatile compounds of its host plant croton californicus muell.-arg. J. Chem. Ecol. 2001, 27:203-216.
    • (2001) J. Chem. Ecol. , vol.27 , pp. 203-216
    • Williams, L.1    Evans, P.E.2    Bowers, W.S.3
  • 110
    • 36549035078 scopus 로고    scopus 로고
    • Production and predator-induced release of volatile chemicals by the plant bug lygus hesperus
    • Byers J.A. Production and predator-induced release of volatile chemicals by the plant bug lygus hesperus. J. Chem. Ecol. 2006, 32:2205-2218.
    • (2006) J. Chem. Ecol. , vol.32 , pp. 2205-2218
    • Byers, J.A.1
  • 111
    • 23844448026 scopus 로고    scopus 로고
    • 4-oxo-2-nonenal is both more neurotoxic and more protein reactive than 4-hydroxy-2-nonenal
    • Lin D., Lee H.G., Liu Q., Perry G., Smith M.A., Sayre L.M. 4-oxo-2-nonenal is both more neurotoxic and more protein reactive than 4-hydroxy-2-nonenal. Chem. Res. Toxicol. 2005, 18:1219-1231.
    • (2005) Chem. Res. Toxicol. , vol.18 , pp. 1219-1231
    • Lin, D.1    Lee, H.G.2    Liu, Q.3    Perry, G.4    Smith, M.A.5    Sayre, L.M.6
  • 112
    • 31844452548 scopus 로고    scopus 로고
    • Identification of 4-oxo-2-hexenal and other direct mutagens formed in model lipid peroxidation reactions as dguo adducts
    • Maekawa M., Kawai K., Takahashi Y., Nakamura H., Watanabe T., Sawa R., Hachisuka K., Kasai H. Identification of 4-oxo-2-hexenal and other direct mutagens formed in model lipid peroxidation reactions as dguo adducts. Chem. Res. Toxicol. 2006, 19:130-138.
    • (2006) Chem. Res. Toxicol. , vol.19 , pp. 130-138
    • Maekawa, M.1    Kawai, K.2    Takahashi, Y.3    Nakamura, H.4    Watanabe, T.5    Sawa, R.6    Hachisuka, K.7    Kasai, H.8
  • 114
    • 34547645204 scopus 로고    scopus 로고
    • A novel 4-oxo-2(e)-nonenal-derived endogenous thiadiazabicyclo glutathione adduct formed during cellular oxidative stress
    • Jian W., Lee S.H., Mesaros C., Oe T., Elipe M.V., Blair I.A. A novel 4-oxo-2(e)-nonenal-derived endogenous thiadiazabicyclo glutathione adduct formed during cellular oxidative stress. Chem. Res. Toxicol. 2007, 20:1008-1018.
    • (2007) Chem. Res. Toxicol. , vol.20 , pp. 1008-1018
    • Jian, W.1    Lee, S.H.2    Mesaros, C.3    Oe, T.4    Elipe, M.V.5    Blair, I.A.6


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