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Evaluation of radical scavenging properties of shikonin
With the aim of developing effective anti-inflammatory drugs, we have been investigating the biochemical effects of shikonin of “Shikon” roots, which is a naphthoquinone with anti-inflammatory and antioxidative properties. Shikonin scavenged reactive oxygen species like hydroxyl radical, superoxide...
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/PMC4186383/ https://www.ncbi.nlm.nih.gov/pubmed/25320455 http://dx.doi.org/10.3164/jcbn.13-107 |
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author | Yoshida, Lucia S. Kohri, Shunji Tsunawaki, Shohko Kakegawa, Tomohito Taniguchi, Taizo Takano-Ohmuro, Hiromi Fujii, Hirotada |
author_facet | Yoshida, Lucia S. Kohri, Shunji Tsunawaki, Shohko Kakegawa, Tomohito Taniguchi, Taizo Takano-Ohmuro, Hiromi Fujii, Hirotada |
author_sort | Yoshida, Lucia S. |
collection | PubMed |
description | With the aim of developing effective anti-inflammatory drugs, we have been investigating the biochemical effects of shikonin of “Shikon” roots, which is a naphthoquinone with anti-inflammatory and antioxidative properties. Shikonin scavenged reactive oxygen species like hydroxyl radical, superoxide anion (O(2)(•−)) and singlet oxygen in previous studies, but its reactivity with reactive oxygen species is not completely understood, and comparison with standard antioxidants is lacking. This study aimed elucidation of the reactivity of shikonin with nitric oxide radical and reactive oxygen species such as alkyl-oxy radical and O(2)(•−). By using electron paramagnetic resonance spectrometry, shikonin was found unable of reacting with nitric oxide radical in a competition assay with oxyhemoglobin. However, shikonin scavenged alkyl-oxy radical from 2,2'-azobis(2-aminopropane) dihydrochloride with oxygen radical absorbance capacity, ORAC of 0.25 relative to Trolox, and showed a strong O(2)(•−)-scavenging ability (42-fold of Trolox; estimated reaction rate constant: 1.7 × 10(5) M(−1)s(−1)) in electron paramagnetic resonance assays with CYPMPO as spin trap. Concerning another source of O(2)(•−), the phagocyte NADPH oxidase (Nox2), shikonin inhibited the Nox2 activity by impairing catalysis when added before enzyme activation (IC(50): 1.1 µM; NADPH oxidation assay). However, shikonin did not affect the preactivated Nox2 activity, although having potential to scavenge produced O(2)(•−). In conclusion, shikonin scavenged O(2)(•−) and alkyl-oxy radical, but not nitric oxide radical. |
format | Online Article Text |
id | pubmed-4186383 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | the Society for Free Radical Research Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-41863832014-10-15 Evaluation of radical scavenging properties of shikonin Yoshida, Lucia S. Kohri, Shunji Tsunawaki, Shohko Kakegawa, Tomohito Taniguchi, Taizo Takano-Ohmuro, Hiromi Fujii, Hirotada J Clin Biochem Nutr Original Article With the aim of developing effective anti-inflammatory drugs, we have been investigating the biochemical effects of shikonin of “Shikon” roots, which is a naphthoquinone with anti-inflammatory and antioxidative properties. Shikonin scavenged reactive oxygen species like hydroxyl radical, superoxide anion (O(2)(•−)) and singlet oxygen in previous studies, but its reactivity with reactive oxygen species is not completely understood, and comparison with standard antioxidants is lacking. This study aimed elucidation of the reactivity of shikonin with nitric oxide radical and reactive oxygen species such as alkyl-oxy radical and O(2)(•−). By using electron paramagnetic resonance spectrometry, shikonin was found unable of reacting with nitric oxide radical in a competition assay with oxyhemoglobin. However, shikonin scavenged alkyl-oxy radical from 2,2'-azobis(2-aminopropane) dihydrochloride with oxygen radical absorbance capacity, ORAC of 0.25 relative to Trolox, and showed a strong O(2)(•−)-scavenging ability (42-fold of Trolox; estimated reaction rate constant: 1.7 × 10(5) M(−1)s(−1)) in electron paramagnetic resonance assays with CYPMPO as spin trap. Concerning another source of O(2)(•−), the phagocyte NADPH oxidase (Nox2), shikonin inhibited the Nox2 activity by impairing catalysis when added before enzyme activation (IC(50): 1.1 µM; NADPH oxidation assay). However, shikonin did not affect the preactivated Nox2 activity, although having potential to scavenge produced O(2)(•−). In conclusion, shikonin scavenged O(2)(•−) and alkyl-oxy radical, but not nitric oxide radical. the Society for Free Radical Research Japan 2014-09 2014-08-05 /pmc/articles/PMC4186383/ /pubmed/25320455 http://dx.doi.org/10.3164/jcbn.13-107 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 Yoshida, Lucia S. Kohri, Shunji Tsunawaki, Shohko Kakegawa, Tomohito Taniguchi, Taizo Takano-Ohmuro, Hiromi Fujii, Hirotada Evaluation of radical scavenging properties of shikonin |
title | Evaluation of radical scavenging properties of shikonin |
title_full | Evaluation of radical scavenging properties of shikonin |
title_fullStr | Evaluation of radical scavenging properties of shikonin |
title_full_unstemmed | Evaluation of radical scavenging properties of shikonin |
title_short | Evaluation of radical scavenging properties of shikonin |
title_sort | evaluation of radical scavenging properties of shikonin |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4186383/ https://www.ncbi.nlm.nih.gov/pubmed/25320455 http://dx.doi.org/10.3164/jcbn.13-107 |
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