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Recent Development of the Molecular and Cellular Mechanisms of Hydrogen Sulfide Gasotransmitter
Hydrogen sulfide has been recently identified as the third biological gasotransmitter, along with the more well studied nitric oxide (NO) and carbon monoxide (CO). Intensive studies on its potential as a therapeutic agent for cardiovascular, inflammatory, infectious and neuropathological diseases ha...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9495975/ https://www.ncbi.nlm.nih.gov/pubmed/36139861 http://dx.doi.org/10.3390/antiox11091788 |
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author | Liu, Jianyun Mesfin, Fikir M. Hunter, Chelsea E. Olson, Kenneth R. Shelley, W. Christopher Brokaw, John P. Manohar, Krishna Markel, Troy A. |
author_facet | Liu, Jianyun Mesfin, Fikir M. Hunter, Chelsea E. Olson, Kenneth R. Shelley, W. Christopher Brokaw, John P. Manohar, Krishna Markel, Troy A. |
author_sort | Liu, Jianyun |
collection | PubMed |
description | Hydrogen sulfide has been recently identified as the third biological gasotransmitter, along with the more well studied nitric oxide (NO) and carbon monoxide (CO). Intensive studies on its potential as a therapeutic agent for cardiovascular, inflammatory, infectious and neuropathological diseases have been undertaken. Here we review the possible direct targets of H(2)S in mammals. H(2)S directly interacts with reactive oxygen/nitrogen species and is involved in redox signaling. H(2)S also reacts with hemeproteins and modulates metal-containing complexes. Once being oxidized, H(2)S can persulfidate proteins by adding -SSH to the amino acid cysteine. These direct modifications by H(2)S have significant impact on cell structure and many cellular functions, such as tight junctions, autophagy, apoptosis, vesicle trafficking, cell signaling, epigenetics and inflammasomes. Therefore, we conclude that H(2)S is involved in many important cellular and physiological processes. Compounds that donate H(2)S to biological systems can be developed as therapeutics for different diseases. |
format | Online Article Text |
id | pubmed-9495975 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-94959752022-09-23 Recent Development of the Molecular and Cellular Mechanisms of Hydrogen Sulfide Gasotransmitter Liu, Jianyun Mesfin, Fikir M. Hunter, Chelsea E. Olson, Kenneth R. Shelley, W. Christopher Brokaw, John P. Manohar, Krishna Markel, Troy A. Antioxidants (Basel) Review Hydrogen sulfide has been recently identified as the third biological gasotransmitter, along with the more well studied nitric oxide (NO) and carbon monoxide (CO). Intensive studies on its potential as a therapeutic agent for cardiovascular, inflammatory, infectious and neuropathological diseases have been undertaken. Here we review the possible direct targets of H(2)S in mammals. H(2)S directly interacts with reactive oxygen/nitrogen species and is involved in redox signaling. H(2)S also reacts with hemeproteins and modulates metal-containing complexes. Once being oxidized, H(2)S can persulfidate proteins by adding -SSH to the amino acid cysteine. These direct modifications by H(2)S have significant impact on cell structure and many cellular functions, such as tight junctions, autophagy, apoptosis, vesicle trafficking, cell signaling, epigenetics and inflammasomes. Therefore, we conclude that H(2)S is involved in many important cellular and physiological processes. Compounds that donate H(2)S to biological systems can be developed as therapeutics for different diseases. MDPI 2022-09-10 /pmc/articles/PMC9495975/ /pubmed/36139861 http://dx.doi.org/10.3390/antiox11091788 Text en © 2022 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 Liu, Jianyun Mesfin, Fikir M. Hunter, Chelsea E. Olson, Kenneth R. Shelley, W. Christopher Brokaw, John P. Manohar, Krishna Markel, Troy A. Recent Development of the Molecular and Cellular Mechanisms of Hydrogen Sulfide Gasotransmitter |
title | Recent Development of the Molecular and Cellular Mechanisms of Hydrogen Sulfide Gasotransmitter |
title_full | Recent Development of the Molecular and Cellular Mechanisms of Hydrogen Sulfide Gasotransmitter |
title_fullStr | Recent Development of the Molecular and Cellular Mechanisms of Hydrogen Sulfide Gasotransmitter |
title_full_unstemmed | Recent Development of the Molecular and Cellular Mechanisms of Hydrogen Sulfide Gasotransmitter |
title_short | Recent Development of the Molecular and Cellular Mechanisms of Hydrogen Sulfide Gasotransmitter |
title_sort | recent development of the molecular and cellular mechanisms of hydrogen sulfide gasotransmitter |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9495975/ https://www.ncbi.nlm.nih.gov/pubmed/36139861 http://dx.doi.org/10.3390/antiox11091788 |
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