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Effects of Food Components That Activate TRPA1 Receptors on Mucosal Ion Transport in the Mouse Intestine
TRPA1 is a ligand-activated cation channel found in the intestine and other tissues. Components of food that stimulate TRPA1 receptors (phytonutrients) include allyl isothiocyanate, cinnamaldehyde and linalool, but these may also act at other receptors. Cells lining the intestinal mucosa are immunor...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5084011/ https://www.ncbi.nlm.nih.gov/pubmed/27735854 http://dx.doi.org/10.3390/nu8100623 |
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author | Fothergill, Linda J. Callaghan, Brid Rivera, Leni R. Lieu, TinaMarie Poole, Daniel P. Cho, Hyun-Jung Bravo, David M. Furness, John B. |
author_facet | Fothergill, Linda J. Callaghan, Brid Rivera, Leni R. Lieu, TinaMarie Poole, Daniel P. Cho, Hyun-Jung Bravo, David M. Furness, John B. |
author_sort | Fothergill, Linda J. |
collection | PubMed |
description | TRPA1 is a ligand-activated cation channel found in the intestine and other tissues. Components of food that stimulate TRPA1 receptors (phytonutrients) include allyl isothiocyanate, cinnamaldehyde and linalool, but these may also act at other receptors. Cells lining the intestinal mucosa are immunoreactive for TRPA1 and Trpa1 mRNA occurs in mucosal extracts, suggesting that the TRPA1 receptor is the target for these agonists. However, in situ hybridisation reveals Trpa1 expression in 5-HT containing enteroendocrine cells, not enterocytes. TRPA1 agonists evoke mucosal secretion, which may be indirect (through release of 5-HT) or direct by activation of enterocytes. We investigated effects of the phytonutrients on transmucosal ion currents in mouse duodenum and colon, and the specificity of the phytonutrients in cells transfected with Trpa1, and in Trpa1-deficient mice. The phytonutrients increased currents in the duodenum with the relative potencies: allyl isothiocyanate (AITC) > cinnamaldehyde > linalool (0.1 to 300 μM). The rank order was similar in the colon, but linalool was ineffective. Responses to AITC were reduced by the TRPA1 antagonist HC-030031 (100 μM), and were greatly diminished in Trpa1−/− duodenum and colon. Responses were not reduced by tetrodotoxin, 5-HT receptor antagonists, or atropine, but inhibition of prostaglandin synthesis reduced responses. Thus, functional TRPA1 channels are expressed by enterocytes of the duodenum and colon. Activation of enterocyte TRPA1 by food components has the potential to facilitate nutrient absorption. |
format | Online Article Text |
id | pubmed-5084011 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-50840112016-11-01 Effects of Food Components That Activate TRPA1 Receptors on Mucosal Ion Transport in the Mouse Intestine Fothergill, Linda J. Callaghan, Brid Rivera, Leni R. Lieu, TinaMarie Poole, Daniel P. Cho, Hyun-Jung Bravo, David M. Furness, John B. Nutrients Article TRPA1 is a ligand-activated cation channel found in the intestine and other tissues. Components of food that stimulate TRPA1 receptors (phytonutrients) include allyl isothiocyanate, cinnamaldehyde and linalool, but these may also act at other receptors. Cells lining the intestinal mucosa are immunoreactive for TRPA1 and Trpa1 mRNA occurs in mucosal extracts, suggesting that the TRPA1 receptor is the target for these agonists. However, in situ hybridisation reveals Trpa1 expression in 5-HT containing enteroendocrine cells, not enterocytes. TRPA1 agonists evoke mucosal secretion, which may be indirect (through release of 5-HT) or direct by activation of enterocytes. We investigated effects of the phytonutrients on transmucosal ion currents in mouse duodenum and colon, and the specificity of the phytonutrients in cells transfected with Trpa1, and in Trpa1-deficient mice. The phytonutrients increased currents in the duodenum with the relative potencies: allyl isothiocyanate (AITC) > cinnamaldehyde > linalool (0.1 to 300 μM). The rank order was similar in the colon, but linalool was ineffective. Responses to AITC were reduced by the TRPA1 antagonist HC-030031 (100 μM), and were greatly diminished in Trpa1−/− duodenum and colon. Responses were not reduced by tetrodotoxin, 5-HT receptor antagonists, or atropine, but inhibition of prostaglandin synthesis reduced responses. Thus, functional TRPA1 channels are expressed by enterocytes of the duodenum and colon. Activation of enterocyte TRPA1 by food components has the potential to facilitate nutrient absorption. MDPI 2016-10-10 /pmc/articles/PMC5084011/ /pubmed/27735854 http://dx.doi.org/10.3390/nu8100623 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Fothergill, Linda J. Callaghan, Brid Rivera, Leni R. Lieu, TinaMarie Poole, Daniel P. Cho, Hyun-Jung Bravo, David M. Furness, John B. Effects of Food Components That Activate TRPA1 Receptors on Mucosal Ion Transport in the Mouse Intestine |
title | Effects of Food Components That Activate TRPA1 Receptors on Mucosal Ion Transport in the Mouse Intestine |
title_full | Effects of Food Components That Activate TRPA1 Receptors on Mucosal Ion Transport in the Mouse Intestine |
title_fullStr | Effects of Food Components That Activate TRPA1 Receptors on Mucosal Ion Transport in the Mouse Intestine |
title_full_unstemmed | Effects of Food Components That Activate TRPA1 Receptors on Mucosal Ion Transport in the Mouse Intestine |
title_short | Effects of Food Components That Activate TRPA1 Receptors on Mucosal Ion Transport in the Mouse Intestine |
title_sort | effects of food components that activate trpa1 receptors on mucosal ion transport in the mouse intestine |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5084011/ https://www.ncbi.nlm.nih.gov/pubmed/27735854 http://dx.doi.org/10.3390/nu8100623 |
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