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Role of Hydrogen Sulfide in the Pathology of Inflammation

Hydrogen sulfide (H(2)S) is a well-known toxic gas that is synthesized in the human body from the amino acids cystathionine, homocysteine, and cysteine by the action of at least two distinct enzymes: cystathionine-γ-lyase and cystathionine-β-synthase. In the past few years, H(2)S has emerged as a no...

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Autor principal: Bhatia, Madhav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3820548/
https://www.ncbi.nlm.nih.gov/pubmed/24278674
http://dx.doi.org/10.6064/2012/159680
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author Bhatia, Madhav
author_facet Bhatia, Madhav
author_sort Bhatia, Madhav
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description Hydrogen sulfide (H(2)S) is a well-known toxic gas that is synthesized in the human body from the amino acids cystathionine, homocysteine, and cysteine by the action of at least two distinct enzymes: cystathionine-γ-lyase and cystathionine-β-synthase. In the past few years, H(2)S has emerged as a novel and increasingly important biological mediator. Imbalances in H(2)S have also been shown to be associated with various disease conditions. However, defining the precise pathophysiology of H(2)S is proving to be a complex challenge. Recent research in our laboratory has shown H(2)S as a novel mediator of inflammation and work in several groups worldwide is currently focused on determining the role of H(2)S in inflammation. H(2)S has been implicated in different inflammatory conditions, such as acute pancreatitis, sepsis, joint inflammation, and chronic obstructive pulmonary disease (COPD). Active research on the role of H(2)S in inflammation will unravel the pathophysiology of its actions in inflammatory conditions and may help develop novel therapeutic approaches for several, as yet incurable, disease conditions.
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spelling pubmed-38205482013-11-25 Role of Hydrogen Sulfide in the Pathology of Inflammation Bhatia, Madhav Scientifica (Cairo) Review Article Hydrogen sulfide (H(2)S) is a well-known toxic gas that is synthesized in the human body from the amino acids cystathionine, homocysteine, and cysteine by the action of at least two distinct enzymes: cystathionine-γ-lyase and cystathionine-β-synthase. In the past few years, H(2)S has emerged as a novel and increasingly important biological mediator. Imbalances in H(2)S have also been shown to be associated with various disease conditions. However, defining the precise pathophysiology of H(2)S is proving to be a complex challenge. Recent research in our laboratory has shown H(2)S as a novel mediator of inflammation and work in several groups worldwide is currently focused on determining the role of H(2)S in inflammation. H(2)S has been implicated in different inflammatory conditions, such as acute pancreatitis, sepsis, joint inflammation, and chronic obstructive pulmonary disease (COPD). Active research on the role of H(2)S in inflammation will unravel the pathophysiology of its actions in inflammatory conditions and may help develop novel therapeutic approaches for several, as yet incurable, disease conditions. Hindawi Publishing Corporation 2012 2012-10-09 /pmc/articles/PMC3820548/ /pubmed/24278674 http://dx.doi.org/10.6064/2012/159680 Text en Copyright © 2012 Madhav Bhatia. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Bhatia, Madhav
Role of Hydrogen Sulfide in the Pathology of Inflammation
title Role of Hydrogen Sulfide in the Pathology of Inflammation
title_full Role of Hydrogen Sulfide in the Pathology of Inflammation
title_fullStr Role of Hydrogen Sulfide in the Pathology of Inflammation
title_full_unstemmed Role of Hydrogen Sulfide in the Pathology of Inflammation
title_short Role of Hydrogen Sulfide in the Pathology of Inflammation
title_sort role of hydrogen sulfide in the pathology of inflammation
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3820548/
https://www.ncbi.nlm.nih.gov/pubmed/24278674
http://dx.doi.org/10.6064/2012/159680
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