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Protective Actions of Epithelial 5-Hydroxytryptamine 4 Receptors in Normal and Inflamed Colon
Stephanie N Spohn1, Francesca Bianco2, Rachel B Scott3
1Neurological Sciences, University of Vermont, Burlington, Vermont.
Background & Aims:
The 5-hydroxytryptamine receptor 4 (5-HT4R or HTR4) is expressed in the colonic epithelium but little is known about its functions there. We examined whether activation of colonic epithelial 5-HT4R protects colons of mice from inflammation.
Methods:
The 5-HT4R agonist tegaserod (1 mg/kg), the 5-HT4R antagonist GR113808 (1 mg/kg), or vehicle (control) were delivered by enema to wild-type or 5-HT4R knockout mice at the onset of, or during, active colitis, induced by administration of dextran sodium sulfate or trinitrobenzene sulfonic acid. Inflammation was measured using the colitis disease activity index and by histologic analysis of intestinal tissues. Epithelial proliferation, wound healing, and resistance to oxidative stress-induced apoptosis were assessed, as was colonic motility.
Results:
Rectal administration of tegaserod reduced the severity of colitis compared with mice given vehicle, and accelerated recovery from active colitis. Rectal tegaserod did not improve colitis in 5-HT4R knockout mice, and intraperitoneally administered tegaserod did not protect wild-type mice from colitis. Tegaserod increased proliferation of crypt epithelial cells. Stimulation of 5-HT4R increased Caco-2 cell migration and reduced oxidative stress-induced apoptosis; these actions were blocked by co-administration of the 5-HT4R antagonist GR113808. In noninflamed colons of wild-type mice not receiving tegaserod, inhibition of 5-HT4Rs resulted in signs of colitis within 3 days. In these mice, epithelial proliferation decreased and bacterial translocation to the liver and spleen was detected. Daily administration of tegaserod increased motility in inflamed colons of guinea pigs and mice, whereas administration of GR113808 disrupted motility in animals without colitis.
Conclusions:
5-HT4R activation maintains motility in healthy colons of mice and guinea pigs, and reduces inflammation in colons of mice with colitis. Agonists might be developed as treatments for patients with inflammatory bowel diseases.
Insights
Activation of the 5-hydroxytryptamine receptor 4 (5-HT4R) in the colon reduces inflammation and improves gut motility. This suggests 5-HT4R agonists could be potential treatments for inflammatory bowel diseases.
Area of Science:
- Gastroenterology
- Pharmacology
- Immunology
Background:
- The 5-hydroxytryptamine receptor 4 (5-HT4R) is present in the colonic epithelium, but its specific functions there are not well understood.
- Investigating the role of 5-HT4R in colonic inflammation is crucial for understanding its potential therapeutic applications.
Purpose of the Study:
- To determine if activating colonic epithelial 5-HT4R can protect against and reduce inflammation in the colon.
- To explore the effects of 5-HT4R activation on epithelial cell proliferation, wound healing, and resistance to apoptosis.
Main Methods:
- Colitis was induced in wild-type and 5-HT4R knockout mice using dextran sodium sulfate or trinitrobenzene sulfonic acid.
- Mice were treated with the 5-HT4R agonist tegaserod or antagonist GR113808 via enema or intraperitoneally.
- Inflammation was assessed using disease activity index and histological analysis; epithelial cell proliferation, wound healing, and apoptosis resistance were also measured.
Main Results:
- Rectal administration of tegaserod significantly reduced colitis severity and accelerated recovery in wild-type mice, but not in knockout mice.
- Tegaserod enhanced epithelial cell proliferation, migration, and resistance to oxidative stress-induced apoptosis.
- Inhibition of 5-HT4R in healthy colons led to colitis signs, decreased proliferation, and bacterial translocation.
Conclusions:
- 5-HT4R activation is essential for maintaining colonic motility in healthy states and reducing inflammation during colitis.
- Targeting 5-HT4R with agonists presents a promising therapeutic strategy for managing inflammatory bowel diseases.
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