Metabolic activation of 2,4,6-trinitrotoluene; a case for ROS-induced cell damage

The explosive compound 2,4,6-trinitrotoluene (TNT) is well known as a major component of munitions. In addition to its potential carcinogenicity and mutagenicity in humans, recent reports have highlighted TNT toxicities in diverse organisms due to its occurrence in the environment. These toxic effec...

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Main Authors: Amma Gyapomah Adomako-Bonsu, Jana Jacobsen, Edmund Maser
Format: Article
Language:English
Published: Elsevier 2024-06-01
Series:Redox Biology
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2213231724000582
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author Amma Gyapomah Adomako-Bonsu
Jana Jacobsen
Edmund Maser
author_facet Amma Gyapomah Adomako-Bonsu
Jana Jacobsen
Edmund Maser
author_sort Amma Gyapomah Adomako-Bonsu
collection DOAJ
description The explosive compound 2,4,6-trinitrotoluene (TNT) is well known as a major component of munitions. In addition to its potential carcinogenicity and mutagenicity in humans, recent reports have highlighted TNT toxicities in diverse organisms due to its occurrence in the environment. These toxic effects have been linked to the intracellular metabolism of TNT, which is generally characterised by redox cycling and the generation of noxious reactive molecules. The reactive intermediates formed, such as nitroso and hydroxylamine compounds, also interact with oxygen molecules and cellular components to cause macromolecular damage and oxidative stress. The current review aims to highlight the crucial role of TNT metabolism in mediating TNT toxicity, via increased generation of reactive oxygen species. Cellular proliferation of reactive species results in depletion of cellular antioxidant enzymes, DNA and protein adduct formation, and oxidative stress. While TNT toxicity is well known, its ability to induce oxidative stress, resulting from its reductive activation, suggests that some of its toxic effects may be caused by its reactive metabolites. Hence, further research on TNT metabolism is imperative to elucidate TNT-induced toxicities.
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spelling doaj.art-3c56c74b9f3e4c87a3188d8160c59c872024-03-25T04:17:32ZengElsevierRedox Biology2213-23172024-06-0172103082Metabolic activation of 2,4,6-trinitrotoluene; a case for ROS-induced cell damageAmma Gyapomah Adomako-Bonsu0Jana Jacobsen1Edmund Maser2Institute of Toxicology and Pharmacology for Natural Scientists, University Medical School Schleswig-Holstein Campus Kiel, Brunswiker Str. 10, 24105, Kiel, GermanyInstitute of Toxicology and Pharmacology for Natural Scientists, University Medical School Schleswig-Holstein Campus Kiel, Brunswiker Str. 10, 24105, Kiel, GermanyCorresponding author. Institute of Toxicology and Pharmacology for Natural Scientists, University Medical School Schleswig-Holstein, Brunswiker Str. 10, 24105, Kiel, Germany.; Institute of Toxicology and Pharmacology for Natural Scientists, University Medical School Schleswig-Holstein Campus Kiel, Brunswiker Str. 10, 24105, Kiel, GermanyThe explosive compound 2,4,6-trinitrotoluene (TNT) is well known as a major component of munitions. In addition to its potential carcinogenicity and mutagenicity in humans, recent reports have highlighted TNT toxicities in diverse organisms due to its occurrence in the environment. These toxic effects have been linked to the intracellular metabolism of TNT, which is generally characterised by redox cycling and the generation of noxious reactive molecules. The reactive intermediates formed, such as nitroso and hydroxylamine compounds, also interact with oxygen molecules and cellular components to cause macromolecular damage and oxidative stress. The current review aims to highlight the crucial role of TNT metabolism in mediating TNT toxicity, via increased generation of reactive oxygen species. Cellular proliferation of reactive species results in depletion of cellular antioxidant enzymes, DNA and protein adduct formation, and oxidative stress. While TNT toxicity is well known, its ability to induce oxidative stress, resulting from its reductive activation, suggests that some of its toxic effects may be caused by its reactive metabolites. Hence, further research on TNT metabolism is imperative to elucidate TNT-induced toxicities.http://www.sciencedirect.com/science/article/pii/S2213231724000582Submerged munitions2,4,6-Trinitrotoluene (TNT) toxicity and carcinogenicityMetabolic activationMarine ecotoxicityHuman toxicity
spellingShingle Amma Gyapomah Adomako-Bonsu
Jana Jacobsen
Edmund Maser
Metabolic activation of 2,4,6-trinitrotoluene; a case for ROS-induced cell damage
Redox Biology
Submerged munitions
2,4,6-Trinitrotoluene (TNT) toxicity and carcinogenicity
Metabolic activation
Marine ecotoxicity
Human toxicity
title Metabolic activation of 2,4,6-trinitrotoluene; a case for ROS-induced cell damage
title_full Metabolic activation of 2,4,6-trinitrotoluene; a case for ROS-induced cell damage
title_fullStr Metabolic activation of 2,4,6-trinitrotoluene; a case for ROS-induced cell damage
title_full_unstemmed Metabolic activation of 2,4,6-trinitrotoluene; a case for ROS-induced cell damage
title_short Metabolic activation of 2,4,6-trinitrotoluene; a case for ROS-induced cell damage
title_sort metabolic activation of 2 4 6 trinitrotoluene a case for ros induced cell damage
topic Submerged munitions
2,4,6-Trinitrotoluene (TNT) toxicity and carcinogenicity
Metabolic activation
Marine ecotoxicity
Human toxicity
url http://www.sciencedirect.com/science/article/pii/S2213231724000582
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