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Experimental colitis in rats induces de novo synthesis of cytokines at distant intestinal sites: role of capsaicin-sensitive primary afferent fibers

Fadi. H. Mourad1,2, Tamim. Hamdi1, Kassem. A. Barada1,2, Nayef. E. Saadé1

1 Department of Anatomy, Cell Biology and Physiology
2 Department of Internal Medicine, American University of Beirut, Beirut-Lebanon PO Box 113-6044, Hamra 110-32090, Beirut, Lebanon

* Corresponding Author: F.H. Mourad, email

European Cytokine Network 2016, 27(2), 41-53. https://doi.org/10.1684/ecn.2016.0376

Abstract

Introduction: Increased levels of pro- and anti-inflammatory cytokines were observed in various segments of histologically-intact small intestine in animal models of acute and chronic colitis. Whether these cytokines are produced locally or spread from the inflamed colon is not known. In addition, the role of gut innervation in this upregulation is not fully understood. Aims: To examine whether cytokines are produced de novo in the small intestine in two rat models of colitis; and to investigate the role of capsaicin-sensitive primary afferents in the synthesis of these inflammatory cytokines. Methods: Colitis was induced by rectal instillation of iodoacetamide (IA) or trinitrobenzene sulphonic acid (TNBS) in adult Sprague-Dawley rats. Using reverse transcriptase (RT) and realtime PCR, TNF-α, and IL-10 mRNA expression was measured in mucosal scrapings of the duodenum, jejunum, ileum and colon at different time intervals after induction of colitis. Capsaicin-sensitive primary afferents (CSPA) were ablated using subcutaneous injections of capsaicin at time 0, 8 and 32 h, and the experiment was repeated at specific time intervals to detect any effect on cytokines expression. Results: TNF-α mRNA expression increased by 3-40 times in the different intestinal segments (p<0.05 to p<0.001), 48h after IA-induced colitis. CSPA ablation completely inhibited this upregulation in the small intestine, but not in the colon. Similar results were obtained in TNBS-induced colitis at 24 h. Intestinal IL-10 mRNA expression significantly decreased at 12 h and then increased by 6-43 times (p<0.05 to p<0.001) 48h after IA administration. This increase was abolished in rats subjected to CSPA ablation except in the colon, where IL-10 further increased by twice (p<0.05). In the TNBS group, there was 4-12- and 4-7-fold increases in small intestinal IL-10 mRNA expression at 1 and 21 days after colitis induction, respectively (both p<0.01). This increase was not observed in rats pretreated with capsaicin. Capsaicin-treated and untreated rats had comparable visual ulcer scores after colitis induction. Conclusion: Inflammatory cytokines are produced de novo in distant intestinal segments in colitis. CSPA fibers play a key role in the upregulation of this synthesis.

Keywords

inflammatory bowel disease, cytokines, TNF-α, IL-10, colitis, intestinal inflammation

Cite This Article

APA Style
Mourad, F.H., Hamdi, T., Barada, K.A., Saadé, N.E. (2016). Experimental colitis in rats induces de novo synthesis of cytokines at distant intestinal sites: role of capsaicin-sensitive primary afferent fibers. European Cytokine Network, 27(2), 41–53. https://doi.org/10.1684/ecn.2016.0376
Vancouver Style
Mourad FH, Hamdi T, Barada KA, Saadé NE. Experimental colitis in rats induces de novo synthesis of cytokines at distant intestinal sites: role of capsaicin-sensitive primary afferent fibers. Eur Cytokine Network. 2016;27(2):41–53. https://doi.org/10.1684/ecn.2016.0376
IEEE Style
F.H. Mourad, T. Hamdi, K.A. Barada, and N.E. Saadé, “Experimental colitis in rats induces de novo synthesis of cytokines at distant intestinal sites: role of capsaicin-sensitive primary afferent fibers,” Eur. Cytokine Network, vol. 27, no. 2, pp. 41–53, 2016. https://doi.org/10.1684/ecn.2016.0376



cc Copyright © 2016 The Author(s). Published by Tech Science Press.
This work is licensed under a Creative Commons Attribution 4.0 International License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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