5-HT 7 receptor efficacy distribution throughout the canine stomach

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Abstract

1 This study aimed to determine, quantify and explain regional differences in the relaxant response to the selective 5-HT 1 and 5-HT 7 receptor agonist 5-carboxamidotryptamine (5-CT) throughout the canine stomach. 2 Longitudinal muscle strips from eight gastric corpus regions and six antrum regions were mounted for isotonic measurement. The 5-CT-induced relaxation was examined on a prostaglandin F 2α-induced submaximal response, expressed as percentage of this response and fitted to the operational model of agonism (OMOA). 5-HT 7 receptor messenger RNA (mRNA) expression was compared by means of quantitative PCR. 3 5-CT inhibited PGF 2α- induced tonic contraction (corpus) and increase of phasic contraction amplitude (antrum). The consistent antagonism produced by the selective 5-HT 7 receptor antagonist SB-269970 (10 nM, pA 2 estimates 8.2-8.9) confirmed that in every region, the inhibition by 5-CT was 5-HT 7 receptor mediated. However, variation in the maximum effect (61-108%) and pEC 50 (6.4-8.6) was observed throughout the different regions. The OMOA explained these differences as differences in the efficacy parameter τ (ratio of receptor density and coupling efficiency; log τ estimates ranging from 0.1 to 2.1). The log τ gradient decreases going from the lesser to the greater curvature. A proportional difference (68%) in the relative expression of 5-HT 7 receptor mRNA between the lesser and the greater curvature indicates that differences in receptor density contribute to the observed functional differences. 4 This study illustrates that 5-HT 7 receptors are present throughout the ventral wall of the canine stomach, but the efficacy (expressed as log τ) is clearly greater close to the lesser curvature. Differences in 5-HT 7 receptor expression at least partially explain the functional differences.

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Janssen, P., Prins, N. H., Peeters, P. J., Zuideveld, K. P., & Lefebvre, R. A. (2004). 5-HT 7 receptor efficacy distribution throughout the canine stomach. British Journal of Pharmacology, 143(3), 331–342. https://doi.org/10.1038/sj.bjp.0705922

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