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Kynurenic Acid in the Digestive System—New Facts, New Challenges

This review provides information on the most recent findings concerning presence, origin, and role of kynurenic acid (KYNA), a tryptophan metabolite, in the digestive system. KYNA is an antagonist of both the ionotropic glutamate receptors and the alpha7 nicotinic acetylcholine receptor, as well as...

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Autores principales: Turski, Michal P., Turska, Monika, Paluszkiewicz, Piotr, Parada-Turska, Jolanta, Oxenkrug, Gregory F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3772988/
https://www.ncbi.nlm.nih.gov/pubmed/24049450
http://dx.doi.org/10.4137/IJTR.S12536
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author Turski, Michal P.
Turska, Monika
Paluszkiewicz, Piotr
Parada-Turska, Jolanta
Oxenkrug, Gregory F.
author_facet Turski, Michal P.
Turska, Monika
Paluszkiewicz, Piotr
Parada-Turska, Jolanta
Oxenkrug, Gregory F.
author_sort Turski, Michal P.
collection PubMed
description This review provides information on the most recent findings concerning presence, origin, and role of kynurenic acid (KYNA), a tryptophan metabolite, in the digestive system. KYNA is an antagonist of both the ionotropic glutamate receptors and the alpha7 nicotinic acetylcholine receptor, as well as an agonist of G-protein coupled GPR35 receptor. Since the GPR35 receptor is mainly present in the gastrointestinal tract, researchers have concentrated on the digestive system in recent years. They have found that KYNA content increases gradually and significantly along the gastrointestinal tract. Interestingly, the concentration of KYNA in the lumen is much higher than in the wall of intestine. It has been documented that KYNA may have a positive influence on the number of pathologies in the gastrointestinal tract, in particular ulcers, colon obstruction, or colitis. Future studies might determine whether it is advisable to supplement KYNA to a human organism.
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spelling pubmed-37729882013-09-18 Kynurenic Acid in the Digestive System—New Facts, New Challenges Turski, Michal P. Turska, Monika Paluszkiewicz, Piotr Parada-Turska, Jolanta Oxenkrug, Gregory F. Int J Tryptophan Res Concise Review This review provides information on the most recent findings concerning presence, origin, and role of kynurenic acid (KYNA), a tryptophan metabolite, in the digestive system. KYNA is an antagonist of both the ionotropic glutamate receptors and the alpha7 nicotinic acetylcholine receptor, as well as an agonist of G-protein coupled GPR35 receptor. Since the GPR35 receptor is mainly present in the gastrointestinal tract, researchers have concentrated on the digestive system in recent years. They have found that KYNA content increases gradually and significantly along the gastrointestinal tract. Interestingly, the concentration of KYNA in the lumen is much higher than in the wall of intestine. It has been documented that KYNA may have a positive influence on the number of pathologies in the gastrointestinal tract, in particular ulcers, colon obstruction, or colitis. Future studies might determine whether it is advisable to supplement KYNA to a human organism. Libertas Academica 2013-09-04 /pmc/articles/PMC3772988/ /pubmed/24049450 http://dx.doi.org/10.4137/IJTR.S12536 Text en © 2013 the author(s), publisher and licensee Libertas Academica Ltd. This is an open access article published under the Creative Commons CC-BY-NC 3.0 license.
spellingShingle Concise Review
Turski, Michal P.
Turska, Monika
Paluszkiewicz, Piotr
Parada-Turska, Jolanta
Oxenkrug, Gregory F.
Kynurenic Acid in the Digestive System—New Facts, New Challenges
title Kynurenic Acid in the Digestive System—New Facts, New Challenges
title_full Kynurenic Acid in the Digestive System—New Facts, New Challenges
title_fullStr Kynurenic Acid in the Digestive System—New Facts, New Challenges
title_full_unstemmed Kynurenic Acid in the Digestive System—New Facts, New Challenges
title_short Kynurenic Acid in the Digestive System—New Facts, New Challenges
title_sort kynurenic acid in the digestive system—new facts, new challenges
topic Concise Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3772988/
https://www.ncbi.nlm.nih.gov/pubmed/24049450
http://dx.doi.org/10.4137/IJTR.S12536
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