» Articles » PMID: 37831752

Protective Actions of a Luminally Acting 5-HT Receptor Agonist in Mouse Models of Colitis

Overview
Date 2023 Oct 13
PMID 37831752
Authors
Affiliations
Soon will be listed here.
Abstract

Background: 5-hydroxytryptamine 4 receptors (5-HT Rs) are expressed in the colonic epithelium, and previous studies have demonstrated that luminal administration of agonists enhances motility, suppresses nociception, and is protective in models of inflammation. We investigated whether stimulation with a luminally acting 5-HT R agonist is comparable to previously tested absorbable compounds.

Methods: The dextran sodium sulfate (DSS), trinitrobenzene sulfonic acid (TNBS), and interleukin 10 knockout (IL-10KO) models of colitis were used to test the protective effects of the luminally acting 5-HT R agonist, 5HT4-LA1, in the absence and presence of a 5-HT R antagonist. The compounds were delivered by enema to mice either before (prevention) or after (recovery) the onset of active colitis. Outcome measure included disease activity index (DAI) and histological evaluation of colon tissue, and effects on wound healing and fecal water content were also assessed.

Key Results: Daily enema of 5HT4-LA1 attenuated the development of, and accelerated recovery from, active colitis. Enema administration of 5HT4-LA1 did not attenuate the development of colitis in 5-HT R knockout mice. Stimulation of 5-HT Rs with 5HT4-LA1 increased Caco-2 cell migration (accelerated wound healing). Daily administration of 5HT4-LA1 did not increase fecal water content in active colitis.

Conclusions And Inferences: Luminally restricted 5-HT R agonists are comparable to absorbable compounds in attenuating and accelerating recovery from active colitis. Luminally acting 5-HT R agonists may be useful as an adjuvant to current inflammatory bowel disease (IBD) treatments to enhance epithelial healing.

References
1.
Li N, Ghia J, Wang H, McClemens J, Cote F, Suehiro Y . Serotonin activates dendritic cell function in the context of gut inflammation. Am J Pathol. 2011; 178(2):662-71. PMC: 3069907. DOI: 10.1016/j.ajpath.2010.10.028. View

2.
Mawe G, Hoffman J . Serotonin signalling in the gut--functions, dysfunctions and therapeutic targets. Nat Rev Gastroenterol Hepatol. 2013; 10(8):473-86. PMC: 4048923. DOI: 10.1038/nrgastro.2013.105. View

3.
Fukudo S, Nakamura M, Hamatani T, Kazumori K, Miwa H . Efficacy and Safety of 5-HT4 Receptor Agonist Minesapride for Irritable Bowel Syndrome with Constipation in a Randomized Controlled Trial. Clin Gastroenterol Hepatol. 2020; 19(3):538-546.e8. DOI: 10.1016/j.cgh.2020.03.019. View

4.
Fang X, Liu S, Wang X, Gao N, Hu H, Wang G . Neurogastroenterology of tegaserod (HTF 919) in the submucosal division of the guinea-pig and human enteric nervous system. Neurogastroenterol Motil. 2007; 20(1):80-93. DOI: 10.1111/j.1365-2982.2007.00983.x. View

5.
Idzko M, Panther E, Stratz C, Muller T, Bayer H, Zissel G . The serotoninergic receptors of human dendritic cells: identification and coupling to cytokine release. J Immunol. 2004; 172(10):6011-9. DOI: 10.4049/jimmunol.172.10.6011. View