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Sulfur mustard induced oxidative stress and its alteration using asoxime (HI-6)
Sulfur mustard (SM) is a blister agent with cytotoxic mechanism of action. There is no suitable treatment based on administration of an antidote. In this study, Wistar rats were exposed to SM in doses of 0–40 mg/kg body weight and treated with the compound HI-6. The treatment provided no significant...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Slovak Toxicology Society SETOX
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3945758/ https://www.ncbi.nlm.nih.gov/pubmed/24678258 http://dx.doi.org/10.2478/intox-2013-0029 |
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author | Pohanka, Miroslav Sobotka, Jakub Svobodova, Hana Stetina, Rudolf |
author_facet | Pohanka, Miroslav Sobotka, Jakub Svobodova, Hana Stetina, Rudolf |
author_sort | Pohanka, Miroslav |
collection | PubMed |
description | Sulfur mustard (SM) is a blister agent with cytotoxic mechanism of action. There is no suitable treatment based on administration of an antidote. In this study, Wistar rats were exposed to SM in doses of 0–40 mg/kg body weight and treated with the compound HI-6. The treatment provided no significant effect on ferric reducing antioxidant power of blood and plasma. However, HI-6 caused an increase in the level of thiobarbituric acid reactive substances. This stressogenic response was presumably the cause of the significant elevation of the blood level of both glutathione reductase and reduced glutathione. HI-6 appears to be suitable for enhancing prophylactically oxidative stress protection from small oxidative insult. |
format | Online Article Text |
id | pubmed-3945758 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Slovak Toxicology Society SETOX |
record_format | MEDLINE/PubMed |
spelling | pubmed-39457582014-03-27 Sulfur mustard induced oxidative stress and its alteration using asoxime (HI-6) Pohanka, Miroslav Sobotka, Jakub Svobodova, Hana Stetina, Rudolf Interdiscip Toxicol Original Article Sulfur mustard (SM) is a blister agent with cytotoxic mechanism of action. There is no suitable treatment based on administration of an antidote. In this study, Wistar rats were exposed to SM in doses of 0–40 mg/kg body weight and treated with the compound HI-6. The treatment provided no significant effect on ferric reducing antioxidant power of blood and plasma. However, HI-6 caused an increase in the level of thiobarbituric acid reactive substances. This stressogenic response was presumably the cause of the significant elevation of the blood level of both glutathione reductase and reduced glutathione. HI-6 appears to be suitable for enhancing prophylactically oxidative stress protection from small oxidative insult. Slovak Toxicology Society SETOX 2013-12 2013-12 /pmc/articles/PMC3945758/ /pubmed/24678258 http://dx.doi.org/10.2478/intox-2013-0029 Text en Copyright © 2013 Slovak Toxicology Society SETOX http://creativecommons.org/licenses/by/2.0/ 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 Pohanka, Miroslav Sobotka, Jakub Svobodova, Hana Stetina, Rudolf Sulfur mustard induced oxidative stress and its alteration using asoxime (HI-6) |
title | Sulfur mustard induced oxidative stress and its alteration using asoxime (HI-6) |
title_full | Sulfur mustard induced oxidative stress and its alteration using asoxime (HI-6) |
title_fullStr | Sulfur mustard induced oxidative stress and its alteration using asoxime (HI-6) |
title_full_unstemmed | Sulfur mustard induced oxidative stress and its alteration using asoxime (HI-6) |
title_short | Sulfur mustard induced oxidative stress and its alteration using asoxime (HI-6) |
title_sort | sulfur mustard induced oxidative stress and its alteration using asoxime (hi-6) |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3945758/ https://www.ncbi.nlm.nih.gov/pubmed/24678258 http://dx.doi.org/10.2478/intox-2013-0029 |
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