New Insights into the Mechanism of on Colitis in Mice: Modulation of the Pain and Immune System.

Mar Drugs

Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, Viale Ferdinando Stagno d'Alcontres, 98166 Messina, Italy.

Published: May 2023

AI Article Synopsis

  • Inflammatory bowel diseases (IBD), including Crohn's disease (CD) and ulcerative colitis (UC), cause symptoms like abdominal pain and diarrhea due to an immune system imbalance.
  • A marine green alga extract has shown potential benefits, including anti-inflammatory and antioxidant effects, in a mouse model of colitis.
  • The study examines the extract's ability to relieve pain and modulate the immune response, suggesting it could be an effective treatment for managing symptoms of IBD.

Article Abstract

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. , 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 extract in a murine model of colitis. In this study, we aimed to examine thoroughly immunomodulatory and pain-relieving properties. Colitis was induced by using the DNBS model (4 mg in 100 μL of 50% ethanol), whereas was administered daily at the dosage of 50 and 100 mg/kg by oral gavage. 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 as a valid approach to counteract immune dysregulation and abdominal discomfort in IBD.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10223675PMC
http://dx.doi.org/10.3390/md21050298DOI Listing

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