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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...

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Detalles Bibliográficos
Autores principales: Deavall, Damian G., Martin, Elizabeth A., Horner, Judith M., Roberts, Ruth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
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.
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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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