1. Spizofurone, a new anti-ulcer agent, increases alkaline secretion in isolated bullfrog duodenal mucosa
- Author
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Hiroshi Satoh, Nobuhiro Inatomi, Hideaki Nagaya, Ikuko Inada, and Yoshitaka Maki
- Subjects
Male ,medicine.medical_specialty ,Duodenum ,medicine.medical_treatment ,Indomethacin ,Stimulation ,In Vitro Techniques ,Biology ,Dinoprostone ,Bullfrog ,1-Methyl-3-isobutylxanthine ,Internal medicine ,medicine ,Animals ,Secretion ,Intestinal Mucosa ,Prostaglandin E2 ,Benzofurans ,Pharmacology ,Rana catesbeiana ,Ussing chamber ,Prostaglandins E ,Anti-ulcer Agent ,Hydrogen-Ion Concentration ,Anti-Ulcer Agents ,Endocrinology ,medicine.anatomical_structure ,Female ,lipids (amino acids, peptides, and proteins) ,Prostaglandin E ,medicine.drug - Abstract
The effect of spizofurone, a new anti-ulcer agent, on alkaline secretion was studied in an isolated sheet of bullfrog proximal duodenal mucosa mounted in an Ussing chamber. Spizofurone (10−4-10−3 M) as well as prostaglandin E2 (PGE2, 10−8-10−5 M) added to the nutrient solution increased alkaline secretion, transmucosal potential difference (PD) and short-circuit current (Isc), in a concentration-dependent manner. The maximum increases in alkaline secretion stimulated by spizofurone and PGE2 were much the same. Spizofurone also showed this effect when added to the secretory solution while PGE2 did not. Treatment with indomethacin partly but significantly inhibited the effect of spizofurone, but did not affect that of PGE2. These results indicate that the increase in alkaline secretion in bullfrog duodenal mucosa seen in the presence of spizofurone is mediated, at least in part, by stimulation of endogenous PGs synthesis.
- Published
- 1986
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