Kynurenic Acid in the Digestive System–-New Facts, New Challenges

Author:

Turski Michal P.1,Turska Monika2,Paluszkiewicz Piotr3,Parada-Turska Jolanta4,Oxenkrug Gregory F.5

Affiliation:

1. Department of Toxicology, Institute of Rural Health, Jaczewskiego, Lublin, Poland.

2. Department of Experimental and Clinical Pharmacology, Medical University, Jaczewskiego, Lublin, Poland.

3. Department of Surgery and Surgical Nursing, Medical University, Chodzki, Lublin, Poland.

4. Department of Rheumatology and Connective Tissue Diseases, Medical University, Jaczewskiego, Lublin, Poland.

5. Department of Psychiatry, Tufts University School of Medicine, Psychiatry and Inflammation Program, Tufts Medical Center, Boston, Massachusetts, USA.

Abstract

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.

Publisher

SAGE Publications

Subject

Molecular Biology,Biochemistry

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