Abstract
1. The aim of this study was to characterize the 5-HT receptors involved in the 5-HT-induced contraction of longitudinal muscle (LM) strips of porcine proximal stomach. This was done in a classical organ bath set-up for isotonic measurement. 2. The concentration-contraction curve to 5-HT was not modified by 5-HT 3 and 5-HT 4 receptor antagonism. Methysergide, ketanserin and mesulergine antagonized the curve to 5-HT. Concomitantly, increasing concentrations of ketanserin and mesulergine progressively revealed a biphasic nature of the 5-HT curve. Ketanserin antagonized the low-affinity receptor while it did not modify the high-affinity receptor. 3. Tetrodotoxin did not influence the concentration-contraction curve to 5-HT neither in the absence nor presence of ketanserin, indicating that nerves are not involved. 4. Ketanserin competitively antagonized the monophasic concentration-response curve to α-Methyl-5-HT, yielding a Schild slope that was not significantly different from unity. After constraining the Schild slope to unity, a pK B estimate of 8.23 ± 0.90 was obtained. This affinity estimate of ketanserin closely approximates previously reported affinities at 5-HT 2A receptors. 5. In the presence of ketanserin (0.1 μM; exposing the high-affinity receptor), a wide range of 5-HT receptor antagonists covering all 5-HT receptors known, was tested. Only methysergide and ritanserin inhibited the response to 5-HT, thus expressing affinity for the high-affinity receptor. This did not reveal the identity of the receptor involved. 6. It can be concluded that 5-HT induces pig proximal stomach (LM) contraction via 5-HT 2A receptors located on smooth muscle. A ketanserin-insensitive phase of contractions could not be characterized between the actually known classes of 5-HT receptors with the pharmacological tools that were used.
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Janssen, P., Prins, N. H., Meulemans, A. L., & Lefebvre, R. A. (2002). Smooth muscle 5-HT 2A receptors mediating contraction of porcine isolated proximal stomach strips. British Journal of Pharmacology, 137(8), 1217–1224. https://doi.org/10.1038/sj.bjp.0704992
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