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Role of Hydrogen Sulfide, Substance P and Adhesion Molecules in Acute Pancreatitis
Inflammation is a natural response to tissue injury. Uncontrolled inflammatory response leads to inflammatory disease. Acute pancreatitis is one of the main reasons for hospitalization amongst gastrointestinal disorders worldwide. It has been demonstrated that endogenous hydrogen sulfide (H(2)S), a...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8622943/ https://www.ncbi.nlm.nih.gov/pubmed/34830018 http://dx.doi.org/10.3390/ijms222212136 |
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author | Kumar, Ayush Bhatia, Madhav |
author_facet | Kumar, Ayush Bhatia, Madhav |
author_sort | Kumar, Ayush |
collection | PubMed |
description | Inflammation is a natural response to tissue injury. Uncontrolled inflammatory response leads to inflammatory disease. Acute pancreatitis is one of the main reasons for hospitalization amongst gastrointestinal disorders worldwide. It has been demonstrated that endogenous hydrogen sulfide (H(2)S), a gasotransmitter and substance P, a neuropeptide, are involved in the inflammatory process in acute pancreatitis. Cell adhesion molecules (CAM) are key players in inflammatory disease. Immunoglobulin (Ig) gene superfamily, selectins, and integrins are involved at different steps of leukocyte migration from blood to the site of injury. When the endothelial cells get activated, the CAMs are upregulated which leads to them interacting with leukocytes. This review summarizes our current understanding of the roles H(2)S, substance P and adhesion molecules play in acute pancreatitis. |
format | Online Article Text |
id | pubmed-8622943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86229432021-11-27 Role of Hydrogen Sulfide, Substance P and Adhesion Molecules in Acute Pancreatitis Kumar, Ayush Bhatia, Madhav Int J Mol Sci Review Inflammation is a natural response to tissue injury. Uncontrolled inflammatory response leads to inflammatory disease. Acute pancreatitis is one of the main reasons for hospitalization amongst gastrointestinal disorders worldwide. It has been demonstrated that endogenous hydrogen sulfide (H(2)S), a gasotransmitter and substance P, a neuropeptide, are involved in the inflammatory process in acute pancreatitis. Cell adhesion molecules (CAM) are key players in inflammatory disease. Immunoglobulin (Ig) gene superfamily, selectins, and integrins are involved at different steps of leukocyte migration from blood to the site of injury. When the endothelial cells get activated, the CAMs are upregulated which leads to them interacting with leukocytes. This review summarizes our current understanding of the roles H(2)S, substance P and adhesion molecules play in acute pancreatitis. MDPI 2021-11-09 /pmc/articles/PMC8622943/ /pubmed/34830018 http://dx.doi.org/10.3390/ijms222212136 Text en © 2021 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 Kumar, Ayush Bhatia, Madhav Role of Hydrogen Sulfide, Substance P and Adhesion Molecules in Acute Pancreatitis |
title | Role of Hydrogen Sulfide, Substance P and Adhesion Molecules in Acute Pancreatitis |
title_full | Role of Hydrogen Sulfide, Substance P and Adhesion Molecules in Acute Pancreatitis |
title_fullStr | Role of Hydrogen Sulfide, Substance P and Adhesion Molecules in Acute Pancreatitis |
title_full_unstemmed | Role of Hydrogen Sulfide, Substance P and Adhesion Molecules in Acute Pancreatitis |
title_short | Role of Hydrogen Sulfide, Substance P and Adhesion Molecules in Acute Pancreatitis |
title_sort | role of hydrogen sulfide, substance p and adhesion molecules in acute pancreatitis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8622943/ https://www.ncbi.nlm.nih.gov/pubmed/34830018 http://dx.doi.org/10.3390/ijms222212136 |
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