Fate of 4-hydroxynonenal in vivo: disposition and metabolic pathways
Tài liệu tham khảo
Alary, 1995, Mercapturic acid conjugates as urinary end metabolites of the lipid peroxidation product 4-hydroxy-nonenal in the rat, Chem. Res. Toxicol., 8, 34, 10.1021/tx00043a004
Alary, 1998, 1,4-Dihydroxynonene mercapturic acid, the major end metabolite of exogenous 4-hydroxy-2-nonenal, is a physiological component of rat and human urine, Chem. Res. Toxicol., 11, 130, 10.1021/tx970139w
Alary, 1998, Identification of novel urinary metabolites of the lipid peroxidation product 4-hydroxy-2-nonenal in rats, Chem. Res. Toxicol., 11, 1368, 10.1021/tx980068g
Alary, 2003, Identification of intermediate pathways of 4-hydroxynonenal metabolism in the rat, Chem. Res. Toxicol., 16, 320, 10.1021/tx025671k
Boon, 1999, Glutathione conjugation of 4-hydroxy-trans-2,3-nonenal in the rat in vivo, the isolated perfused liver and erythrocytes, Toxicol. Appl. Pharmacol., 159, 214, 10.1006/taap.1999.8742
Bruenner, 1995, Direct characterization of protein adducts of the lipid peroxidation product 4-hydroxy-2-nonenal using electrospray mass spectrometry, Chem. Res. Toxicol., 8, 552, 10.1021/tx00046a009
Crouzet, F., 1996. Métabolisme in vivo d’un produit de la peroxydation lipidique, le 4-hydroxynonénal. Ph.D. Thesis, Institut National Polytechnique de Toulouse, Toulouse
Danielson, 1987, Structure-activity relationships of 4-hydroxyalkenals in the conjugation catalysed by mammalian glutathione transferase, Biochem. J., 247, 707, 10.1042/bj2470707
De Zwart, 1996, Disposition in rat of [2-3H]-trans-4-hydroxy-2,3-nonenal, a product of lipid peroxidation, Xenobiotica, 26, 1087, 10.3109/00498259609167424
Dianzani, 1998, 4-Hydroxynonenal and cell signaling, Free Rad. Res., 28, 553, 10.3109/10715769809065811
Esterbauer, 1970, Kinetics of the reaction of sulfhydryl compounds with alpha-beta-unsaturated aldehydes in aqueous system, Monatsh. Chem., 101, 782, 10.1007/BF00909898
Esterbauer, 1991, Chemistry and biochemistry of 4-hydroxynonenal, malonaldehyde and related aldehydes, Free Rad. Biol. Med., 11, 81, 10.1016/0891-5849(91)90192-6
Guéraud, 1999, In vivo involvement of cytochrome P450 4A family in the oxidative metabolism of the lipid peroxidation product trans-4-hydroxy-2-nonenal, using PPAR α-deficient mice, J. Lip. Res., 40, 152, 10.1016/S0022-2275(20)33350-2
Hinchman, 1991, Intrahepatic conversion of a glutathione conjugate to its mercapturic acid. Metabolism of 1-chloro-2,4-dinitrobenzene in isolated perfused rat and guinea pig livers, J. Biol. Chem., 266, 22179, 10.1016/S0021-9258(18)54551-8
Hiratsuka, 2001, (S)-preferential detoxification of 4-hydroxy-2(E)-nonenal enantiomers by hepatic glutathione S-transferase isoforms in guinea-pigs and rats, Biochem. J., 355, 237, 10.1042/0264-6021:3550237
Hubatsch, 1998, Human glutathione transferaseA4-4:an alpha class enzyme with high catalytic efficiency in the conjugation of 4-hydroxynonenal and other genotoxic products of lipid peroxidation, Biochem. J., 330, 175, 10.1042/bj3300175
Laurent, 1999, Analysis in the rat of 4-hydroxynonenal metabolites excreted in bile: evidence of enterohepatic circulation of these byproducts of lipid peroxidation, Chem. Res. Toxicol., 12, 887, 10.1021/tx9900425
Nadkarni, 1995, Structural definition of early lysine and histidine adduction chemistry of 4-hydroxynonenal, Chem. Res. Toxicol., 8, 284, 10.1021/tx00044a014
Nair, 1999, Etheno DNA-base adducts from endogenous reactive species, Mutat. Res., 424, 59, 10.1016/S0027-5107(99)00008-1
Okada, 1999, 4-Hydroxy-2-nonenal-mediated impairment of intracellular proteolysis during oxidative stress: identification of proteasomes as target molecules, J. Biol. Chem., 274, 23787, 10.1074/jbc.274.34.23787
Parola, 1999, 4-Hydroxynonenal as a biological signal: molecular basis and pathophysiological implications, Antioxid. Redox Signal., 1, 255, 10.1089/ars.1999.1.3-255
Poli, 2000, 4-Hydroxynonenal in the pathomechanisms of oxidative stress, IUBMB Life., 50, 315, 10.1080/15216540051081092
Schauenstein, 1968, Uber die Bindung von 4-hydroxy-2,3-enalen an protein SH-grupen, Z. Naturforsch., 23b, 316, 10.1515/znb-1968-0306
Siems, 1997, Metabolic fate of 4-hydroxynonenal in hepatocytes: 1,4-dihydroxynonene is not the main product, J. Lipid. Res., 38, 612, 10.1016/S0022-2275(20)37269-2
Srivastava, 1995, Lipid peroxidation product, 4-hydroxynonenal and its conjugate with GSH are excellent substrates of bovine lens aldose reductase, Biochem. Biophys. Res. Commun., 217, 741, 10.1006/bbrc.1995.2835
Toyokuni, 2000, Serum 4-hydroxy-2-nonenal-modified albumin is elevated in patients with type 2 diabetes mellitus, Antioxid. Redox Signal., 2, 681, 10.1089/ars.2000.2.4-681
Winter, 1987, Distribution of trans-4-hydroxy-2-hexenal and tandem mass spectrometric detection of its urinary mercapturic acid in the rat, Drug Metab. Dispos., 15, 608