NAD+ in sulfur mustard toxicity
•Sulfur mustard (SM) and its derivatives are potent toxicants.•The molecular mechanisms behind SM-induced toxicity are not fully understood.•The paper discusses the role of NAD + in SM toxicity.•The beneficial effects of NAD + precursors in SM toxicity are also discussed. Sulfur mustard (SM) is a to...
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Published in | Toxicology letters Vol. 324; pp. 95 - 103 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
15.05.2020
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Subjects | |
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Abstract | •Sulfur mustard (SM) and its derivatives are potent toxicants.•The molecular mechanisms behind SM-induced toxicity are not fully understood.•The paper discusses the role of NAD + in SM toxicity.•The beneficial effects of NAD + precursors in SM toxicity are also discussed.
Sulfur mustard (SM) is a toxicant and chemical warfare agent with strong vesicant properties. The mechanisms behind SM-induced toxicity are not fully understood and no antidote or effective therapy against SM exists. Both, the risk of SM release in asymmetric conflicts or terrorist attacks and the usage of SM-derived nitrogen mustards as cancer chemotherapeutics, render the mechanisms of mustard-induced toxicity a highly relevant research subject. Herein, we review a central role of the abundant cellular molecule nicotinamide adenine dinucleotide (NAD+) in molecular mechanisms underlying SM toxicity. We also discuss the potential beneficial effects of NAD+ precursors in counteracting SM-induced damage. |
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AbstractList | Sulfur mustard (SM) is a toxicant and chemical warfare agent with strong vesicant properties. The mechanisms behind SM-induced toxicity are not fully understood and no antidote or effective therapy against SM exists. Both, the risk of SM release in asymmetric conflicts or terrorist attacks and the usage of SM-derived nitrogen mustards as cancer chemotherapeutics, render the mechanisms of mustard-induced toxicity a highly relevant research subject. Herein, we review a central role of the abundant cellular molecule nicotinamide adenine dinucleotide (NAD
) in molecular mechanisms underlying SM toxicity. We also discuss the potential beneficial effects of NAD
precursors in counteracting SM-induced damage. Sulfur mustard (SM) is a toxicant and chemical warfare agent with strong vesicant properties. The mechanisms behind SM-induced toxicity are not fully understood and no antidote or effective therapy against SM exists. Both, the risk of SM release in asymmetric conflicts or terrorist attacks and the usage of SM-derived nitrogen mustards as cancer chemotherapeutics, render the mechanisms of mustard-induced toxicity a highly relevant research subject. Herein, we review a central role of the abundant cellular molecule nicotinamide adenine dinucleotide (NAD+) in molecular mechanisms underlying SM toxicity. We also discuss the potential beneficial effects of NAD+ precursors in counteracting SM-induced damage.Sulfur mustard (SM) is a toxicant and chemical warfare agent with strong vesicant properties. The mechanisms behind SM-induced toxicity are not fully understood and no antidote or effective therapy against SM exists. Both, the risk of SM release in asymmetric conflicts or terrorist attacks and the usage of SM-derived nitrogen mustards as cancer chemotherapeutics, render the mechanisms of mustard-induced toxicity a highly relevant research subject. Herein, we review a central role of the abundant cellular molecule nicotinamide adenine dinucleotide (NAD+) in molecular mechanisms underlying SM toxicity. We also discuss the potential beneficial effects of NAD+ precursors in counteracting SM-induced damage. •Sulfur mustard (SM) and its derivatives are potent toxicants.•The molecular mechanisms behind SM-induced toxicity are not fully understood.•The paper discusses the role of NAD + in SM toxicity.•The beneficial effects of NAD + precursors in SM toxicity are also discussed. Sulfur mustard (SM) is a toxicant and chemical warfare agent with strong vesicant properties. The mechanisms behind SM-induced toxicity are not fully understood and no antidote or effective therapy against SM exists. Both, the risk of SM release in asymmetric conflicts or terrorist attacks and the usage of SM-derived nitrogen mustards as cancer chemotherapeutics, render the mechanisms of mustard-induced toxicity a highly relevant research subject. Herein, we review a central role of the abundant cellular molecule nicotinamide adenine dinucleotide (NAD+) in molecular mechanisms underlying SM toxicity. We also discuss the potential beneficial effects of NAD+ precursors in counteracting SM-induced damage. |
Author | Ruszkiewicz, Joanna A. Bürkle, Alexander Mangerich, Aswin |
Author_xml | – sequence: 1 givenname: Joanna A. surname: Ruszkiewicz fullname: Ruszkiewicz, Joanna A. email: joanna.ruszkiewicz@uni-konstanz.de – sequence: 2 givenname: Alexander orcidid: 0000-0003-1069-2656 surname: Bürkle fullname: Bürkle, Alexander email: alexander.buerkle@uni-konstanz.de – sequence: 3 givenname: Aswin orcidid: 0000-0001-9742-2338 surname: Mangerich fullname: Mangerich, Aswin email: aswin.mangerich@uni-konstanz.de, amang@mit.edu |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32017979$$D View this record in MEDLINE/PubMed |
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Keywords | NAD Sirtuins Nicotinamide adenine dinucleotide Cytotoxicity PARP Sulfur mustard |
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Snippet | •Sulfur mustard (SM) and its derivatives are potent toxicants.•The molecular mechanisms behind SM-induced toxicity are not fully understood.•The paper... Sulfur mustard (SM) is a toxicant and chemical warfare agent with strong vesicant properties. The mechanisms behind SM-induced toxicity are not fully... |
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SubjectTerms | Animals Chemical Warfare Agents - toxicity Cytotoxicity Dietary Supplements Humans Mustard Gas - toxicity NAD NAD - administration & dosage NAD - physiology Niacinamide - administration & dosage Nicotinamide adenine dinucleotide Oxidative Stress - drug effects PARP Poly(ADP-ribose) Polymerases - metabolism Reactive Nitrogen Species - metabolism Sirtuins Sirtuins - antagonists & inhibitors Sulfur mustard |
Title | NAD+ in sulfur mustard toxicity |
URI | https://dx.doi.org/10.1016/j.toxlet.2020.01.024 https://www.ncbi.nlm.nih.gov/pubmed/32017979 https://www.proquest.com/docview/2351502997 |
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