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The Impact of Drugs on Hydrogen Sulfide Homeostasis in Mammals
Mammalian cells and tissues have the capacity to generate hydrogen sulfide gas (H(2)S) via catabolic routes involving cysteine metabolism. H(2)S acts on cell signaling cascades that are necessary in many biochemical and physiological roles important in the heart, brain, liver, kidney, urogenital tra...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10135325/ https://www.ncbi.nlm.nih.gov/pubmed/37107283 http://dx.doi.org/10.3390/antiox12040908 |
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author | Alsaeedi, Asrar Welham, Simon Rose, Peter Zhu, Yi-Zhun |
author_facet | Alsaeedi, Asrar Welham, Simon Rose, Peter Zhu, Yi-Zhun |
author_sort | Alsaeedi, Asrar |
collection | PubMed |
description | Mammalian cells and tissues have the capacity to generate hydrogen sulfide gas (H(2)S) via catabolic routes involving cysteine metabolism. H(2)S acts on cell signaling cascades that are necessary in many biochemical and physiological roles important in the heart, brain, liver, kidney, urogenital tract, and cardiovascular and immune systems of mammals. Diminished levels of this molecule are observed in several pathophysiological conditions including heart disease, diabetes, obesity, and immune function. Interestingly, in the last two decades, it has become apparent that some commonly prescribed pharmacological drugs can impact the expression and activities of enzymes responsible for hydrogen sulfide production in cells and tissues. Therefore, the current review provides an overview of the studies that catalogue key drugs and their impact on hydrogen sulfide production in mammals. |
format | Online Article Text |
id | pubmed-10135325 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-101353252023-04-28 The Impact of Drugs on Hydrogen Sulfide Homeostasis in Mammals Alsaeedi, Asrar Welham, Simon Rose, Peter Zhu, Yi-Zhun Antioxidants (Basel) Review Mammalian cells and tissues have the capacity to generate hydrogen sulfide gas (H(2)S) via catabolic routes involving cysteine metabolism. H(2)S acts on cell signaling cascades that are necessary in many biochemical and physiological roles important in the heart, brain, liver, kidney, urogenital tract, and cardiovascular and immune systems of mammals. Diminished levels of this molecule are observed in several pathophysiological conditions including heart disease, diabetes, obesity, and immune function. Interestingly, in the last two decades, it has become apparent that some commonly prescribed pharmacological drugs can impact the expression and activities of enzymes responsible for hydrogen sulfide production in cells and tissues. Therefore, the current review provides an overview of the studies that catalogue key drugs and their impact on hydrogen sulfide production in mammals. MDPI 2023-04-11 /pmc/articles/PMC10135325/ /pubmed/37107283 http://dx.doi.org/10.3390/antiox12040908 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Alsaeedi, Asrar Welham, Simon Rose, Peter Zhu, Yi-Zhun The Impact of Drugs on Hydrogen Sulfide Homeostasis in Mammals |
title | The Impact of Drugs on Hydrogen Sulfide Homeostasis in Mammals |
title_full | The Impact of Drugs on Hydrogen Sulfide Homeostasis in Mammals |
title_fullStr | The Impact of Drugs on Hydrogen Sulfide Homeostasis in Mammals |
title_full_unstemmed | The Impact of Drugs on Hydrogen Sulfide Homeostasis in Mammals |
title_short | The Impact of Drugs on Hydrogen Sulfide Homeostasis in Mammals |
title_sort | impact of drugs on hydrogen sulfide homeostasis in mammals |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10135325/ https://www.ncbi.nlm.nih.gov/pubmed/37107283 http://dx.doi.org/10.3390/antiox12040908 |
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