Alary J - Search Results

1

Identification of intermediate pathways of 4-hydroxynonenal metabolism in the rat.

Alary J, Fernandez Y, Debrauwer L, Perdu E, Guéraud F. Alary J, et al. Chem Res Toxicol. 2003 Mar;16(3):320-7. doi: 10.1021/tx025671k. Chem Res Toxicol. 2003. PMID: 12641432

2

Fate of 4-hydroxynonenal in vivo: disposition and metabolic pathways.

Alary J, Guéraud F, Cravedi JP. Alary J, et al. Mol Aspects Med. 2003 Aug-Oct;24(4-5):177-87. doi: 10.1016/s0098-2997(03)00012-8. Mol Aspects Med. 2003. PMID: 12892995 Review.

3

Enzyme immunoassay for a urinary metabolite of 4-hydroxynonenal as a marker of lipid peroxidation.

Guéraud F, Peiro G, Bernard H, Alary J, Créminon C, Debrauwer L, Rathahao E, Drumare MF, Canlet C, Wal JM, Bories G. Guéraud F, et al. Among authors: alary j. Free Radic Biol Med. 2006 Jan 1;40(1):54-62. doi: 10.1016/j.freeradbiomed.2005.08.011. Epub 2005 Sep 2. Free Radic Biol Med. 2006. PMID: 16337879

4

Enantioselective metabolism of (R)- and (S)-4-hydroxy-2-nonenal in rat.

Guéraud F, Crouzet F, Alary J, Rao D, Debrauwer L, Laurent F, Cravedi JP. Guéraud F, et al. Among authors: alary j. Biofactors. 2005;24(1-4):97-104. doi: 10.1002/biof.5520240111. Biofactors. 2005. PMID: 16403968

5

Chloramphenicol oxamylethanolamine as an end product of chloramphenicol metabolism in rat and humans: evidence for the formation of a phospholipid adduct.

Cravedi JP, Perdu-Durand E, Baradat M, Alary J, Debrauwer L, Bories G. Cravedi JP, et al. Among authors: alary j. Chem Res Toxicol. 1995 Jul-Aug;8(5):642-8. doi: 10.1021/tx00047a003. Chem Res Toxicol. 1995. PMID: 7548746

6

Mercapturic acid conjugates as urinary end metabolites of the lipid peroxidation product 4-hydroxy-2-nonenal in the rat.

Alary J, Bravais F, Cravedi JP, Debrauwer L, Rao D, Bories G. Alary J, et al. Chem Res Toxicol. 1995 Jan-Feb;8(1):34-9. doi: 10.1021/tx00043a004. Chem Res Toxicol. 1995. PMID: 7703364

7

1,4-Dihydroxynonene mercapturic acid, the major end metabolite of exogenous 4-hydroxy-2-nonenal, is a physiological component of rat and human urine.

Alary J, Debrauwer L, Fernandez Y, Cravedi JP, Rao D, Bories G. Alary J, et al. Chem Res Toxicol. 1998 Feb;11(2):130-5. doi: 10.1021/tx970139w. Chem Res Toxicol. 1998. PMID: 9511904

8

Identification of novel urinary metabolites of the lipid peroxidation product 4-hydroxy-2-nonenal in rats.

Alary J, Debrauwer L, Fernandez Y, Paris A, Cravedi JP, Dolo L, Rao D, Bories G. Alary J, et al. Chem Res Toxicol. 1998 Nov;11(11):1368-76. doi: 10.1021/tx980068g. Chem Res Toxicol. 1998. PMID: 9815199

9

In vivo involvement of cytochrome P450 4A family in the oxidative metabolism of the lipid peroxidation product trans-4-hydroxy-2-nonenal, using PPARalpha-deficient mice.

Guéraud F, Alary J, Costet P, Debrauwer L, Dolo L, Pineau T, Paris A. Guéraud F, et al. Among authors: alary j. J Lipid Res. 1999 Jan;40(1):152-9. J Lipid Res. 1999. PMID: 9869661 Free article.

10

Analysis in the rat of 4-hydroxynonenal metabolites excreted in bile: evidence of enterohepatic circulation of these byproducts of lipid peroxidation.

Laurent A, Alary J, Debrauwer L, Cravedi JP. Laurent A, et al. Among authors: alary j. Chem Res Toxicol. 1999 Oct;12(10):887-94. doi: 10.1021/tx9900425. Chem Res Toxicol. 1999. PMID: 10525263

Within 4 h of injection, the bile accounted for 19.5% (+/-2.8%) of the injected radioactivity, whereas only 3% was found in the feces within 48 h [Alary, J., et al. (1995) Chem. Res. Toxicol. 8, 34-39]. The extent of HNE enterohepatic recycling was estimated utilizi …

Within 4 h of injection, the bile accounted for 19.5% (+/-2.8%) of the injected radioactivity, whereas only 3% was found in the feces within …

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