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Updated: May 19, 2026

Induction of Murine Intestinal Inflammation by Adoptive Transfer of Effector CD4+CD45RBhigh T Cells into Immunodeficient Mice
Published on: April 21, 2015
Transient receptor potential vanilloid 4 blockade protects against experimental colitis in mice: a new strategy for
J Fichna1, A Mokrowiecka, A I Cygankiewicz
1Snyder Institute for Chronic Diseases, University of Calgary, Calgary, AB, Canada.
Abstract:
Recent reports suggested that the activation of Transient Receptor Potential Vanilloid 4 (TRPV4) receptors in the gastrointestinal tract has pro-inflammatory effects. In this study, we demonstrated for the first time that TRPV4 mRNA expression is up-regulated in patients with inflammatory bowel diseases (IBD). Furthermore, selective blockade of TRPV4 in the 2,4,6-trinitrobenzenesulfonic acid animal model alleviates colitis and pain associated with the intestinal inflammation. Our study indicates that TRPV4 may play a role in mechanisms of defense in intestinal inflammation and that TRPV4 may be an attractive target for future systemic or topic anti-inflammatory treatment in patients with IBD.
Insights
Transient Receptor Potential Vanilloid 4 (TRPV4) is upregulated in inflammatory bowel diseases (IBD). Blocking TRPV4 alleviates colitis and pain, suggesting it as a therapeutic target for IBD.
Area of Science:
- Gastroenterology
- Immunology
- Pharmacology
Background:
- Emerging evidence links Transient Receptor Potential Vanilloid 4 (TRPV4) activation in the gut to inflammation.
- The specific role of TRPV4 in inflammatory bowel diseases (IBD) remains largely unexplored.
Purpose of the Study:
- To investigate the expression of TRPV4 in IBD patients.
- To evaluate the therapeutic potential of TRPV4 blockade in an experimental model of colitis.
Main Methods:
- Quantitative analysis of TRPV4 mRNA expression in IBD patient samples.
- Administration of a selective TRPV4 antagonist in the 2,4,6-trinitrobenzenesulfonic acid-induced colitis model in animals.
Main Results:
- TRPV4 mRNA expression was significantly increased in patients with inflammatory bowel diseases.
- Selective TRPV4 blockade markedly reduced colitis severity and associated pain in the animal model.
- These findings highlight the involvement of TRPV4 in the pathophysiology of intestinal inflammation.
Conclusions:
- TRPV4 is upregulated in inflammatory bowel diseases.
- Targeting TRPV4 offers a promising strategy for managing intestinal inflammation and pain in IBD patients.
- TRPV4 represents a potential therapeutic target for novel anti-inflammatory treatments in IBD.
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