Characterization of the contractile response induced by 5-methoxytryptamine in rat stomach fundus strips

This study examined effects of 5-methoxytryptamine (5-MOT), an agonist at 5-HT 4 and 5-HT 2B receptors, on the contractile response and acetylcholine release in rat stomach fundus strips. 5-MOT (10 −9 − 10 −5 M) produced a concentration-dependent increase in the contraction, while it evoked acetylch...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:European journal of pharmacology 1996-12, Vol.318 (2), p.403-409
Hauptverfasser: Amemiya, Norihito, Hatta, Shinichi, Takemura, Haruo, Ohshika, Hideyo
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:This study examined effects of 5-methoxytryptamine (5-MOT), an agonist at 5-HT 4 and 5-HT 2B receptors, on the contractile response and acetylcholine release in rat stomach fundus strips. 5-MOT (10 −9 − 10 −5 M) produced a concentration-dependent increase in the contraction, while it evoked acetylcholine release in a ‘bell-shaped’ concentration-dependent manner. Atropine reduced 5-MOT (10 −8 − 10 −6 M)-induced contractions, but it had little effect on the contractions evoked by higher concentrations. 5-MOT-induced contraction and acetylcholine release were inhibited by SDZ 205–557 (2-methoxy-4-amino-5-chloro-benzoic acid 2-[diethylamino] ethyl ester), a 5-HT 4 receptor antagonist. In the presence of atropine, both SDZ 205–557 and yohimbine, a 5-HT 2B receptor antagonist, inhibited the contraction. In the presence of tetrodotoxin, the contraction was inhibited by yohimbine, but not by SDZ –557. These results suggest that the contractile action of 5-MOT in rat stomach fundus involves atropine-sensitive and atropine-resistant components. The sensitive contraction appears to be mediated through 5-HT 4 receptors located on cholinergic neurons, whereas the resistant contraction is mediated through 5-HT 4 receptors located on non-cholinergic neurons and through 5-HT 2B receptors.
ISSN:0014-2999
1879-0712
DOI:10.1016/S0014-2999(96)00777-7