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Reactions of kynurenic acid with hypobromous acid and hypochlorous acid

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...

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Autores principales: Suzuki, Toshinori, Morishita, Hiroyuki, Fukuhara, Kosumo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: the Society for Free Radical Research Japan 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8129975/
https://www.ncbi.nlm.nih.gov/pubmed/34025023
http://dx.doi.org/10.3164/jcbn.20-62
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author Suzuki, Toshinori
Morishita, Hiroyuki
Fukuhara, Kosumo
author_facet Suzuki, Toshinori
Morishita, Hiroyuki
Fukuhara, Kosumo
author_sort Suzuki, Toshinori
collection PubMed
description 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(1H)-quinolinone as a by-product. Free amino acids suppressed the reactions of kynurenic acid with HOBr and HOCl. Taurine suppressed the HOCl reaction but not the HOBr reaction. An eosinophil peroxidase system containing H(2)O(2), NaCl, and NaBr reacted with kynurenic acid, generating 3-bromokynurenic acid under mildly acidic conditions. Although a myeloperoxidase system containing H(2)O(2) and NaCl reacted with kynurenic acid to generate 3-chlorokynurenic acid under mildly acidic conditions, the product was altered to 3-bromokynurenic acid by addition of NaBr to the system. These results suggest that 3-bromokynurenic acid and 3-chlorokynurenic acid may be generated from kynurenic acid at inflammation sites in humans, although their formation will be suppressed by coexistent amino acids.
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spelling pubmed-81299752021-05-20 Reactions of kynurenic acid with hypobromous acid and hypochlorous acid Suzuki, Toshinori Morishita, Hiroyuki Fukuhara, Kosumo J Clin Biochem Nutr Original Article 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(1H)-quinolinone as a by-product. Free amino acids suppressed the reactions of kynurenic acid with HOBr and HOCl. Taurine suppressed the HOCl reaction but not the HOBr reaction. An eosinophil peroxidase system containing H(2)O(2), NaCl, and NaBr reacted with kynurenic acid, generating 3-bromokynurenic acid under mildly acidic conditions. Although a myeloperoxidase system containing H(2)O(2) and NaCl reacted with kynurenic acid to generate 3-chlorokynurenic acid under mildly acidic conditions, the product was altered to 3-bromokynurenic acid by addition of NaBr to the system. These results suggest that 3-bromokynurenic acid and 3-chlorokynurenic acid may be generated from kynurenic acid at inflammation sites in humans, although their formation will be suppressed by coexistent amino acids. the Society for Free Radical Research Japan 2021-05 2020-10-31 /pmc/articles/PMC8129975/ /pubmed/34025023 http://dx.doi.org/10.3164/jcbn.20-62 Text en Copyright © 2021 JCBN https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ).
spellingShingle Original Article
Suzuki, Toshinori
Morishita, Hiroyuki
Fukuhara, Kosumo
Reactions of kynurenic acid with hypobromous acid and hypochlorous acid
title Reactions of kynurenic acid with hypobromous acid and hypochlorous acid
title_full Reactions of kynurenic acid with hypobromous acid and hypochlorous acid
title_fullStr Reactions of kynurenic acid with hypobromous acid and hypochlorous acid
title_full_unstemmed Reactions of kynurenic acid with hypobromous acid and hypochlorous acid
title_short Reactions of kynurenic acid with hypobromous acid and hypochlorous acid
title_sort reactions of kynurenic acid with hypobromous acid and hypochlorous acid
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8129975/
https://www.ncbi.nlm.nih.gov/pubmed/34025023
http://dx.doi.org/10.3164/jcbn.20-62
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