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Hydrogen Sulfide Metabolizing Enzymes in the Intestinal Mucosa in Pediatric and Adult Inflammatory Bowel Disease

Hydrogen sulfide (H(2)S) is a toxic gas that has important regulatory functions. In the colon, H(2)S can be produced and detoxified endogenously. Both too little and too much H(2)S exposure are associated with inflammatory bowel disease (IBD), a chronic intestinal disease mainly classified as Crohn’...

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Autores principales: Stummer, Nathalie, Weghuber, Daniel, Feichtinger, René G., Huber, Sara, Mayr, Johannes A., Kofler, Barbara, Neureiter, Daniel, Klieser, Eckhard, Hochmann, Sarah, Lauth, Wanda, Schneider, Anna M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9686699/
https://www.ncbi.nlm.nih.gov/pubmed/36421421
http://dx.doi.org/10.3390/antiox11112235
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author Stummer, Nathalie
Weghuber, Daniel
Feichtinger, René G.
Huber, Sara
Mayr, Johannes A.
Kofler, Barbara
Neureiter, Daniel
Klieser, Eckhard
Hochmann, Sarah
Lauth, Wanda
Schneider, Anna M.
author_facet Stummer, Nathalie
Weghuber, Daniel
Feichtinger, René G.
Huber, Sara
Mayr, Johannes A.
Kofler, Barbara
Neureiter, Daniel
Klieser, Eckhard
Hochmann, Sarah
Lauth, Wanda
Schneider, Anna M.
author_sort Stummer, Nathalie
collection PubMed
description Hydrogen sulfide (H(2)S) is a toxic gas that has important regulatory functions. In the colon, H(2)S can be produced and detoxified endogenously. Both too little and too much H(2)S exposure are associated with inflammatory bowel disease (IBD), a chronic intestinal disease mainly classified as Crohn’s disease (CD) and ulcerative colitis (UC). As the pathogenesis of IBD remains elusive, this study’s aim was to investigate potential differences in the expression of H(2)S-metabolizing enzymes in normal aging and IBD. Intestinal mucosal biopsies of 25 adults and 22 children with IBD along with those of 26 healthy controls were stained immunohistochemically for cystathionine-γ-lyase (CSE), 3-mercapto-sulfurtransferase (3-MST), ethylmalonic encephalopathy 1 protein (ETHE1), sulfide:quinone oxidoreductase (SQOR) and thiosulfate sulfurtransferase (TST). Expression levels were calculated by multiplication of the staining intensity and percentage of positively stained cells. Healthy adults showed an overall trend towards lower expression of H(2)S-metabolizing enzymes than healthy children. Adults with IBD also tended to have lower expression compared to controls. A similar trend was seen in the enzyme expression of children with IBD compared to controls. These results indicate an age-related decrease in the expression of H(2)S-metabolizing enzymes and a dysfunctional H(2)S metabolism in IBD, which was less pronounced in children.
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spelling pubmed-96866992022-11-25 Hydrogen Sulfide Metabolizing Enzymes in the Intestinal Mucosa in Pediatric and Adult Inflammatory Bowel Disease Stummer, Nathalie Weghuber, Daniel Feichtinger, René G. Huber, Sara Mayr, Johannes A. Kofler, Barbara Neureiter, Daniel Klieser, Eckhard Hochmann, Sarah Lauth, Wanda Schneider, Anna M. Antioxidants (Basel) Article Hydrogen sulfide (H(2)S) is a toxic gas that has important regulatory functions. In the colon, H(2)S can be produced and detoxified endogenously. Both too little and too much H(2)S exposure are associated with inflammatory bowel disease (IBD), a chronic intestinal disease mainly classified as Crohn’s disease (CD) and ulcerative colitis (UC). As the pathogenesis of IBD remains elusive, this study’s aim was to investigate potential differences in the expression of H(2)S-metabolizing enzymes in normal aging and IBD. Intestinal mucosal biopsies of 25 adults and 22 children with IBD along with those of 26 healthy controls were stained immunohistochemically for cystathionine-γ-lyase (CSE), 3-mercapto-sulfurtransferase (3-MST), ethylmalonic encephalopathy 1 protein (ETHE1), sulfide:quinone oxidoreductase (SQOR) and thiosulfate sulfurtransferase (TST). Expression levels were calculated by multiplication of the staining intensity and percentage of positively stained cells. Healthy adults showed an overall trend towards lower expression of H(2)S-metabolizing enzymes than healthy children. Adults with IBD also tended to have lower expression compared to controls. A similar trend was seen in the enzyme expression of children with IBD compared to controls. These results indicate an age-related decrease in the expression of H(2)S-metabolizing enzymes and a dysfunctional H(2)S metabolism in IBD, which was less pronounced in children. MDPI 2022-11-12 /pmc/articles/PMC9686699/ /pubmed/36421421 http://dx.doi.org/10.3390/antiox11112235 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 Article
Stummer, Nathalie
Weghuber, Daniel
Feichtinger, René G.
Huber, Sara
Mayr, Johannes A.
Kofler, Barbara
Neureiter, Daniel
Klieser, Eckhard
Hochmann, Sarah
Lauth, Wanda
Schneider, Anna M.
Hydrogen Sulfide Metabolizing Enzymes in the Intestinal Mucosa in Pediatric and Adult Inflammatory Bowel Disease
title Hydrogen Sulfide Metabolizing Enzymes in the Intestinal Mucosa in Pediatric and Adult Inflammatory Bowel Disease
title_full Hydrogen Sulfide Metabolizing Enzymes in the Intestinal Mucosa in Pediatric and Adult Inflammatory Bowel Disease
title_fullStr Hydrogen Sulfide Metabolizing Enzymes in the Intestinal Mucosa in Pediatric and Adult Inflammatory Bowel Disease
title_full_unstemmed Hydrogen Sulfide Metabolizing Enzymes in the Intestinal Mucosa in Pediatric and Adult Inflammatory Bowel Disease
title_short Hydrogen Sulfide Metabolizing Enzymes in the Intestinal Mucosa in Pediatric and Adult Inflammatory Bowel Disease
title_sort hydrogen sulfide metabolizing enzymes in the intestinal mucosa in pediatric and adult inflammatory bowel disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9686699/
https://www.ncbi.nlm.nih.gov/pubmed/36421421
http://dx.doi.org/10.3390/antiox11112235
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