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New Insights into the Mechanism of Ulva pertusa on Colitis in Mice: Modulation of the Pain and Immune System
Inflammatory bowel diseases (IBDs) involving Crohn’s disease (CD) and ulcerative colitis (UC) are gastrointestinal (GI) disorders in which abdominal pain, discomfort, and diarrhea are the major symptoms. The immune system plays an important role in the pathogenesis of IBD and, as indicated by severa...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10223675/ https://www.ncbi.nlm.nih.gov/pubmed/37233492 http://dx.doi.org/10.3390/md21050298 |
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author | Ardizzone, Alessio Mannino, Deborah Capra, Anna Paola Repici, Alberto Filippone, Alessia Esposito, Emanuela Campolo, Michela |
author_facet | Ardizzone, Alessio Mannino, Deborah Capra, Anna Paola Repici, Alberto Filippone, Alessia Esposito, Emanuela Campolo, Michela |
author_sort | Ardizzone, Alessio |
collection | PubMed |
description | Inflammatory bowel diseases (IBDs) involving Crohn’s disease (CD) and ulcerative colitis (UC) are gastrointestinal (GI) disorders in which abdominal pain, discomfort, and diarrhea are the major symptoms. The immune system plays an important role in the pathogenesis of IBD and, as indicated by several clinical studies, both innate and adaptative immune response has the faculty to induce gut inflammation in UC patients. An inappropriate mucosal immune response to normal intestinal constituents is a main feature of UC, thus leading to an imbalance in local pro- and anti-inflammatory species. Ulva pertusa, a marine green alga, is known for its important biological properties, which could represent a source of beneficial effects in various human pathologies. We have already demonstrated the anti-inflammatory, antioxidant, and antiapoptotic effects of an Ulva pertusa extract in a murine model of colitis. In this study, we aimed to examine thoroughly Ulva pertusa immunomodulatory and pain-relieving properties. Colitis was induced by using the DNBS model (4 mg in 100 μL of 50% ethanol), whereas Ulva pertusa was administered daily at the dosage of 50 and 100 mg/kg by oral gavage. Ulva pertusa treatments have been shown to relieve abdominal pain while modulating innate and adaptative immune-inflammatory responses. This powerful immunomodulatory activity was specifically linked with TLR4 and NLRP3 inflammasome modulation. In conclusion, our data suggest Ulva pertusa as a valid approach to counteract immune dysregulation and abdominal discomfort in IBD. |
format | Online Article Text |
id | pubmed-10223675 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102236752023-05-28 New Insights into the Mechanism of Ulva pertusa on Colitis in Mice: Modulation of the Pain and Immune System Ardizzone, Alessio Mannino, Deborah Capra, Anna Paola Repici, Alberto Filippone, Alessia Esposito, Emanuela Campolo, Michela Mar Drugs Article Inflammatory bowel diseases (IBDs) involving Crohn’s disease (CD) and ulcerative colitis (UC) are gastrointestinal (GI) disorders in which abdominal pain, discomfort, and diarrhea are the major symptoms. The immune system plays an important role in the pathogenesis of IBD and, as indicated by several clinical studies, both innate and adaptative immune response has the faculty to induce gut inflammation in UC patients. An inappropriate mucosal immune response to normal intestinal constituents is a main feature of UC, thus leading to an imbalance in local pro- and anti-inflammatory species. Ulva pertusa, a marine green alga, is known for its important biological properties, which could represent a source of beneficial effects in various human pathologies. We have already demonstrated the anti-inflammatory, antioxidant, and antiapoptotic effects of an Ulva pertusa extract in a murine model of colitis. In this study, we aimed to examine thoroughly Ulva pertusa immunomodulatory and pain-relieving properties. Colitis was induced by using the DNBS model (4 mg in 100 μL of 50% ethanol), whereas Ulva pertusa was administered daily at the dosage of 50 and 100 mg/kg by oral gavage. Ulva pertusa treatments have been shown to relieve abdominal pain while modulating innate and adaptative immune-inflammatory responses. This powerful immunomodulatory activity was specifically linked with TLR4 and NLRP3 inflammasome modulation. In conclusion, our data suggest Ulva pertusa as a valid approach to counteract immune dysregulation and abdominal discomfort in IBD. MDPI 2023-05-13 /pmc/articles/PMC10223675/ /pubmed/37233492 http://dx.doi.org/10.3390/md21050298 Text en © 2023 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 Ardizzone, Alessio Mannino, Deborah Capra, Anna Paola Repici, Alberto Filippone, Alessia Esposito, Emanuela Campolo, Michela New Insights into the Mechanism of Ulva pertusa on Colitis in Mice: Modulation of the Pain and Immune System |
title | New Insights into the Mechanism of Ulva pertusa on Colitis in Mice: Modulation of the Pain and Immune System |
title_full | New Insights into the Mechanism of Ulva pertusa on Colitis in Mice: Modulation of the Pain and Immune System |
title_fullStr | New Insights into the Mechanism of Ulva pertusa on Colitis in Mice: Modulation of the Pain and Immune System |
title_full_unstemmed | New Insights into the Mechanism of Ulva pertusa on Colitis in Mice: Modulation of the Pain and Immune System |
title_short | New Insights into the Mechanism of Ulva pertusa on Colitis in Mice: Modulation of the Pain and Immune System |
title_sort | new insights into the mechanism of ulva pertusa on colitis in mice: modulation of the pain and immune system |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10223675/ https://www.ncbi.nlm.nih.gov/pubmed/37233492 http://dx.doi.org/10.3390/md21050298 |
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