Denatonium and 6-n-Propyl-2-thiouracil, Agonists of Bitter Taste Receptor, Inhibit Contraction of Various Types of Smooth Muscles in the Rat and Mouse

• Published in: Biological & pharmaceutical bulletin 2016/01/01, Vol.39(1), pp.33-41
• Main Authors: Sakai, Hiroyasu, Sato, Ken, Kai, Yuki, Chiba, Yoshihiko, Narita, Minoru
• Format: Article
• Language: English
• Subjects: Animals; aorta; bitter-taste type-2 receptor; bronchus; Carbachol - pharmacology; Humans; ileum; Male; Mice; Mice, Inbred C57BL; Muscle Contraction - drug effects; Muscle, Smooth - drug effects; Potassium - pharmacology; Propylthiouracil - pharmacology; Quaternary Ammonium Compounds - pharmacology; Rats; Receptors, G-Protein-Coupled - agonists; smooth muscle contraction; Sodium Fluoride - pharmacology
• ISSN: 0918-6158; 1347-5215
• DOI: 10.1248/bpb.b15-00426

Recently the global expression of taste 2 receptors (TAS2Rs) on smooth muscle cells in human airways was demonstrated. Here, the effects of agonists of taste receptor, type 2, denatonium and 6-n-propyl-2-thiouracil, on smooth-muscle contraction were examined in the rat and mouse. Contractions induced by carbachol (CCh), high K+, and sodium fluoride, but not calyculin-A, were inhibited significantly in the presence of a TAS2R agonist in the bronchial smooth muscle of mice. The contraction induced by CCh was inhibited by TAS2R agonists in ileal smooth muscle. Phenylephrine-induced contraction was also inhibited by TAS2R agonists in aortic smooth muscle. Gastrointestinal motility and blood pressure were attenuated by administration of TAS2R agonists in vivo. These findings suggest that TAS2R may be receptor for endogenous biologically active substances as well as for bitter tastes on the tongue. TAS2R signaling could be employed in the development of anti-asthmatic, anti-spasmodic, and anti-hypertensive drugs.