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Drug-Induced Oxidative Stress and Toxicity
Reactive oxygen species (ROS) are a byproduct of normal metabolism and have roles in cell signaling and homeostasis. Species include oxygen radicals and reactive nonradicals. Mechanisms exist that regulate cellular levels of ROS, as their reactive nature may otherwise cause damage to key cellular co...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3420138/ https://www.ncbi.nlm.nih.gov/pubmed/22919381 http://dx.doi.org/10.1155/2012/645460 |
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author | Deavall, Damian G. Martin, Elizabeth A. Horner, Judith M. Roberts, Ruth |
author_facet | Deavall, Damian G. Martin, Elizabeth A. Horner, Judith M. Roberts, Ruth |
author_sort | Deavall, Damian G. |
collection | PubMed |
description | Reactive oxygen species (ROS) are a byproduct of normal metabolism and have roles in cell signaling and homeostasis. Species include oxygen radicals and reactive nonradicals. Mechanisms exist that regulate cellular levels of ROS, as their reactive nature may otherwise cause damage to key cellular components including DNA, protein, and lipid. When the cellular antioxidant capacity is exceeded, oxidative stress can result. Pleiotropic deleterious effects of oxidative stress are observed in numerous disease states and are also implicated in a variety of drug-induced toxicities. In this paper, we examine the nature of ROS-induced damage on key cellular targets of oxidative stress. We also review evidence implicating ROS in clinically relevant, drug-related side effects including doxorubicin-induced cardiac damage, azidothymidine-induced myopathy, and cisplatin-induced ototoxicity. |
format | Online Article Text |
id | pubmed-3420138 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-34201382012-08-23 Drug-Induced Oxidative Stress and Toxicity Deavall, Damian G. Martin, Elizabeth A. Horner, Judith M. Roberts, Ruth J Toxicol Review Article Reactive oxygen species (ROS) are a byproduct of normal metabolism and have roles in cell signaling and homeostasis. Species include oxygen radicals and reactive nonradicals. Mechanisms exist that regulate cellular levels of ROS, as their reactive nature may otherwise cause damage to key cellular components including DNA, protein, and lipid. When the cellular antioxidant capacity is exceeded, oxidative stress can result. Pleiotropic deleterious effects of oxidative stress are observed in numerous disease states and are also implicated in a variety of drug-induced toxicities. In this paper, we examine the nature of ROS-induced damage on key cellular targets of oxidative stress. We also review evidence implicating ROS in clinically relevant, drug-related side effects including doxorubicin-induced cardiac damage, azidothymidine-induced myopathy, and cisplatin-induced ototoxicity. Hindawi Publishing Corporation 2012 2012-08-05 /pmc/articles/PMC3420138/ /pubmed/22919381 http://dx.doi.org/10.1155/2012/645460 Text en Copyright © 2012 Damian G. Deavall et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Deavall, Damian G. Martin, Elizabeth A. Horner, Judith M. Roberts, Ruth Drug-Induced Oxidative Stress and Toxicity |
title | Drug-Induced Oxidative Stress and Toxicity |
title_full | Drug-Induced Oxidative Stress and Toxicity |
title_fullStr | Drug-Induced Oxidative Stress and Toxicity |
title_full_unstemmed | Drug-Induced Oxidative Stress and Toxicity |
title_short | Drug-Induced Oxidative Stress and Toxicity |
title_sort | drug-induced oxidative stress and toxicity |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3420138/ https://www.ncbi.nlm.nih.gov/pubmed/22919381 http://dx.doi.org/10.1155/2012/645460 |
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