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Redox biology of hydrogen sulfide: Implications for physiology, pathophysiology, and pharmacology()

Hydrogen sulfide (H(2)S) has emerged as a critical mediator of multiple physiological processes in mammalian systems. The pathways involved in the production, consumption, and mechanism of action of H(2)S appear to be sensitive to alterations in the cellular redox state and O(2) tension. Indeed, the...

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Detalles Bibliográficos
Autores principales: Stein, Asaf, Bailey, Shannon M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3685875/
https://www.ncbi.nlm.nih.gov/pubmed/23795345
http://dx.doi.org/10.1016/j.redox.2012.11.006
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author Stein, Asaf
Bailey, Shannon M.
author_facet Stein, Asaf
Bailey, Shannon M.
author_sort Stein, Asaf
collection PubMed
description Hydrogen sulfide (H(2)S) has emerged as a critical mediator of multiple physiological processes in mammalian systems. The pathways involved in the production, consumption, and mechanism of action of H(2)S appear to be sensitive to alterations in the cellular redox state and O(2) tension. Indeed, the catabolism of H(2)S through a putative oxidation pathway, the sulfide quinone oxido-reductase system, is highly dependent on O(2) tension. Dysregulation of H(2)S homeostasis has also been implicated in numerous pathological conditions and diseases. In this review, the chemistry and the main physiological actions of H(2)S are presented. Some examples highlighting the cytoprotective actions of H(2)S within the context of cardiovascular disease are also reported. Elucidation of the redox biology of H(2)S will enable the development of new pharmacological agents based on this intriguing new redox cellular signal.
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spelling pubmed-36858752013-09-10 Redox biology of hydrogen sulfide: Implications for physiology, pathophysiology, and pharmacology() Stein, Asaf Bailey, Shannon M. Redox Biol Mini Review Hydrogen sulfide (H(2)S) has emerged as a critical mediator of multiple physiological processes in mammalian systems. The pathways involved in the production, consumption, and mechanism of action of H(2)S appear to be sensitive to alterations in the cellular redox state and O(2) tension. Indeed, the catabolism of H(2)S through a putative oxidation pathway, the sulfide quinone oxido-reductase system, is highly dependent on O(2) tension. Dysregulation of H(2)S homeostasis has also been implicated in numerous pathological conditions and diseases. In this review, the chemistry and the main physiological actions of H(2)S are presented. Some examples highlighting the cytoprotective actions of H(2)S within the context of cardiovascular disease are also reported. Elucidation of the redox biology of H(2)S will enable the development of new pharmacological agents based on this intriguing new redox cellular signal. Elsevier 2013-01-18 /pmc/articles/PMC3685875/ /pubmed/23795345 http://dx.doi.org/10.1016/j.redox.2012.11.006 Text en © 2013 The Authors http://creativecommons.org/licenses/BY-license/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
spellingShingle Mini Review
Stein, Asaf
Bailey, Shannon M.
Redox biology of hydrogen sulfide: Implications for physiology, pathophysiology, and pharmacology()
title Redox biology of hydrogen sulfide: Implications for physiology, pathophysiology, and pharmacology()
title_full Redox biology of hydrogen sulfide: Implications for physiology, pathophysiology, and pharmacology()
title_fullStr Redox biology of hydrogen sulfide: Implications for physiology, pathophysiology, and pharmacology()
title_full_unstemmed Redox biology of hydrogen sulfide: Implications for physiology, pathophysiology, and pharmacology()
title_short Redox biology of hydrogen sulfide: Implications for physiology, pathophysiology, and pharmacology()
title_sort redox biology of hydrogen sulfide: implications for physiology, pathophysiology, and pharmacology()
topic Mini Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3685875/
https://www.ncbi.nlm.nih.gov/pubmed/23795345
http://dx.doi.org/10.1016/j.redox.2012.11.006
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