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Scavenging rate constants of hydrophilic antioxidants against multiple reactive oxygen species
Scavenging rate constants of eight hydrophilic antioxidants, including caffeic acid, chlorogenic acid, genistein, glutathione, N-acetylcysteine, rutin, trolox, and uric acid against multiple ROS, namely superoxide anion, hydroxyl radical, singlet oxygen, and alkoxyl radical were determined with the...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
the Society for Free Radical Research Japan
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3947969/ https://www.ncbi.nlm.nih.gov/pubmed/24688213 http://dx.doi.org/10.3164/jcbn.13-53 |
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author | Sueishi, Yoshimi Hori, Masashi Ishikawa, Misa Matsu-ura, Keiko Kamogawa, Erisa Honda, Yusaku Kita, Masakazu Ohara, Keishi |
author_facet | Sueishi, Yoshimi Hori, Masashi Ishikawa, Misa Matsu-ura, Keiko Kamogawa, Erisa Honda, Yusaku Kita, Masakazu Ohara, Keishi |
author_sort | Sueishi, Yoshimi |
collection | PubMed |
description | Scavenging rate constants of eight hydrophilic antioxidants, including caffeic acid, chlorogenic acid, genistein, glutathione, N-acetylcysteine, rutin, trolox, and uric acid against multiple ROS, namely superoxide anion, hydroxyl radical, singlet oxygen, and alkoxyl radical were determined with the electron spin resonance method. Direct flash photolysis measurement of the second-order rate constant in the reaction of alkoxyl radical plus the spin trap 5,5-dimethyl-pyrroline N-oxide made it possible to evaluate scavenging rate constants in antioxidants. The magnitudes of scavenging rate constants were notably dependent on the character of each ROS and the overall rate constants were highest in hydroxyl radical scavenging and the lowest in superoxide anion. The highest scavenging rate constant against superoxide anion was obtained by chlorogenic acid (2.9 × 10(5) M(−1) s(−1)) and the lowest was by N-acetylcysteine (5.0 × 10(2) M(−1) s(−1)). For singlet oxygen, the highest was by glutathione (9.4 × 10(8) M(−1) s(−1)) and the lowest was by uric acid (2.3 × 10(6) M(−1) s(−1)). All other numbers are listed and illustrated. Redox potential measurements of the antioxidants indicated that the antioxidants are likely to react with superoxide anion and singlet oxygen through electron transfer processes. |
format | Online Article Text |
id | pubmed-3947969 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | the Society for Free Radical Research Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-39479692014-03-31 Scavenging rate constants of hydrophilic antioxidants against multiple reactive oxygen species Sueishi, Yoshimi Hori, Masashi Ishikawa, Misa Matsu-ura, Keiko Kamogawa, Erisa Honda, Yusaku Kita, Masakazu Ohara, Keishi J Clin Biochem Nutr Original Article Scavenging rate constants of eight hydrophilic antioxidants, including caffeic acid, chlorogenic acid, genistein, glutathione, N-acetylcysteine, rutin, trolox, and uric acid against multiple ROS, namely superoxide anion, hydroxyl radical, singlet oxygen, and alkoxyl radical were determined with the electron spin resonance method. Direct flash photolysis measurement of the second-order rate constant in the reaction of alkoxyl radical plus the spin trap 5,5-dimethyl-pyrroline N-oxide made it possible to evaluate scavenging rate constants in antioxidants. The magnitudes of scavenging rate constants were notably dependent on the character of each ROS and the overall rate constants were highest in hydroxyl radical scavenging and the lowest in superoxide anion. The highest scavenging rate constant against superoxide anion was obtained by chlorogenic acid (2.9 × 10(5) M(−1) s(−1)) and the lowest was by N-acetylcysteine (5.0 × 10(2) M(−1) s(−1)). For singlet oxygen, the highest was by glutathione (9.4 × 10(8) M(−1) s(−1)) and the lowest was by uric acid (2.3 × 10(6) M(−1) s(−1)). All other numbers are listed and illustrated. Redox potential measurements of the antioxidants indicated that the antioxidants are likely to react with superoxide anion and singlet oxygen through electron transfer processes. the Society for Free Radical Research Japan 2014-03 2014-02-21 /pmc/articles/PMC3947969/ /pubmed/24688213 http://dx.doi.org/10.3164/jcbn.13-53 Text en Copyright © 2014 JCBN This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Sueishi, Yoshimi Hori, Masashi Ishikawa, Misa Matsu-ura, Keiko Kamogawa, Erisa Honda, Yusaku Kita, Masakazu Ohara, Keishi Scavenging rate constants of hydrophilic antioxidants against multiple reactive oxygen species |
title | Scavenging rate constants of hydrophilic antioxidants against multiple reactive oxygen species |
title_full | Scavenging rate constants of hydrophilic antioxidants against multiple reactive oxygen species |
title_fullStr | Scavenging rate constants of hydrophilic antioxidants against multiple reactive oxygen species |
title_full_unstemmed | Scavenging rate constants of hydrophilic antioxidants against multiple reactive oxygen species |
title_short | Scavenging rate constants of hydrophilic antioxidants against multiple reactive oxygen species |
title_sort | scavenging rate constants of hydrophilic antioxidants against multiple reactive oxygen species |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3947969/ https://www.ncbi.nlm.nih.gov/pubmed/24688213 http://dx.doi.org/10.3164/jcbn.13-53 |
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