Reactions of kynurenic acid with hypobromous acid and hypochlorous acid.

eosinophil peroxidase hypobromous acid hypochlorous acid kynurenic acid myeloperoxidase

Journal

Journal of clinical biochemistry and nutrition
ISSN: 0912-0009
Titre abrégé: J Clin Biochem Nutr
Pays: Japan
ID NLM: 8700907

Informations de publication

Date de publication:
May 2021
Historique:
received: 14 04 2020
accepted: 31 08 2020
entrez: 24 5 2021
pubmed: 25 5 2021
medline: 25 5 2021
Statut: ppublish

Résumé

Kynurenic acid, a tryptophan metabolite, acts as antagonist or agonist of several receptors. Hypobromous acid (HOBr) and hypochlorous acid (HOCl) are generated by eosinophils and neutrophils. At inflammation sites, kynurenic acid may encounter HOBr and HOCl to generate products. When kynurenic acid was incubated with HOBr under neutral conditions, kynurenic acid generated a single product almost exclusively. This was identified as 3-bromokynurenic acid. Kynurenic acid reacted with HOCl, generating two products. The major product was identified as 3-chlorokynurenic acid with its oxidative decarboxylation product, 3-chloro-4-hydroxy-2(1

Identifiants

pubmed: 34025023
doi: 10.3164/jcbn.20-62
pii: DN/JST.JSTAGE/jcbn/20-62
pmc: PMC8129975
doi:

Types de publication

Journal Article

Langues

eng

Pagination

215-220

Informations de copyright

Copyright © 2021 JCBNCopyright © 2021 JCBN.

Déclaration de conflit d'intérêts

No potential conflicts of interest were disclosed.

Références

Arch Biochem Biophys. 1962 Mar;96:465-7
pubmed: 13909511
Ann Clin Biochem. 2016 May;53(Pt 3):357-64
pubmed: 25829462
Proc Natl Acad Sci U S A. 2001 Oct 9;98(21):11961-6
pubmed: 11593004
J Immunol. 2001 May 1;166(9):5763-72
pubmed: 11313420
Arch Biochem Biophys. 2006 Jan 15;445(2):256-60
pubmed: 16297853
Redox Rep. 1997 Feb;3(1):3-15
pubmed: 27414766
Chem Pharm Bull (Tokyo). 2019;67(11):1250-1254
pubmed: 31685753
Clin Biochem. 1980 Dec;13(6):277-8
pubmed: 7214696
Int J Tryptophan Res. 2017 Mar 15;10:1178646917691938
pubmed: 28469468
Metabolites. 2019 Nov 01;9(11):
pubmed: 31683910
Parkinsons Dis. 2011;2011:716859
pubmed: 21687761
Anal Biochem. 2002 Jan 15;300(2):252-9
pubmed: 11779118
N Engl J Med. 1998 May 28;338(22):1592-600
pubmed: 9603798
J Pharmacol Exp Ther. 1986 Jan;236(1):293-9
pubmed: 2867215
J Biol Chem. 1995 Feb 17;270(7):2906-13
pubmed: 7852368
Front Neurosci. 2015 Oct 21;9:372
pubmed: 26539073
Neurosci Lett. 2001 Nov 2;313(1-2):96-8
pubmed: 11684348
J Biol Chem. 2010 Mar 19;285(12):9282-91
pubmed: 20081197
Int J Tryptophan Res. 2013 Sep 04;6:47-55
pubmed: 24049450
Proc Natl Acad Sci U S A. 1988 Sep;85(17):6547-50
pubmed: 2842779
J Biol Chem. 2001 Mar 16;276(11):7867-75
pubmed: 11096071
J Psychiatry Neurosci. 2010 May;35(3):195-9
pubmed: 20420770
J Neurosci. 2001 Oct 1;21(19):7463-73
pubmed: 11567036
Adv Exp Med Biol. 2003;527:395-400
pubmed: 15206756
Water Res. 2014 Jan 1;48:15-42
pubmed: 24184020
J Leukoc Biol. 2013 Feb;93(2):185-98
pubmed: 23066164
Mol Pharmacol. 1992 May;41(5):914-22
pubmed: 1375317
Chem Pharm Bull (Tokyo). 2019;67(10):1164-1167
pubmed: 31582637
J Biol Chem. 2006 Aug 4;281(31):22021-22028
pubmed: 16754668
Pharmacol Biochem Behav. 2019 Feb;177:12-19
pubmed: 30586559
J Leukoc Biol. 1990 Aug;48(2):174-82
pubmed: 2370482
Water Res. 2017 Mar 1;110:91-101
pubmed: 27998787
J Am Chem Soc. 1946 Dec;68(12):2570-4
pubmed: 20282396
Science. 1986 Oct 10;234(4773):200-3
pubmed: 3018933
Methods Enzymol. 1999;300:88-105
pubmed: 9919513
Biochem Pharmacol. 1990 Aug 15;40(4):851-7
pubmed: 1696821

Auteurs

Toshinori Suzuki (T)

School of Pharmacy, Shujitsu University, 1-6-1 Nishigawara, Okayama 703-8516, Japan.

Hiroyuki Morishita (H)

School of Pharmacy, Shujitsu University, 1-6-1 Nishigawara, Okayama 703-8516, Japan.

Kosumo Fukuhara (K)

School of Pharmacy, Shujitsu University, 1-6-1 Nishigawara, Okayama 703-8516, Japan.

Classifications MeSH