
Caffeic acid phenethyl ester (CAPE), one of the major components of propolis (honeybee resin), has demonstrated a wide spectrum of activities including suppression of eicosanoids by inhibition of cyclooxygenase-1 and cyclooxygenase-2 enzyme activities. The aim of this study was to investigate the effect of CAPE on basal and secretagogues-stimulated gastric acid secretion in vitro. In the isolated, lumen-perfused, stomach preparation of mouse, CAPE (10-100 microM) did not affect the basal gastric acid secretion nor the secretion stimulated by histamine, pentagastrin, isobutyl methylxanthine and high levels of K+. By contrast, CAPE increased the gastric acid secretion induced by the muscarinic receptor agonist, 5-methylfurmethide (5-MEF). CAPE also inhibited the acetylcholinesterase activity in an in vitro colorimetric assay. Eserine (10 microM), a well known acetylcholinesterase inhibitor, also increased 5-MEF-stimulated acid secretion. Our results show that CAPE increases gastric acid secretion stimulated by an acetylcholine agonist receptor likely through inhibition of acetylcholinesterase activity.
Male, Mice, Inbred ICR, Dose-Response Relationship, Drug, Nifedipine, Physostigmine, In Vitro Techniques, Phenylethyl Alcohol, Gastric Acid, Mice, Caffeic Acids, Gastrointestinal Agents, Gastric Mucosa, 1-Methyl-3-isobutylxanthine, Muscarine, Acetylcholinesterase, Potassium, Animals, Pentagastrin, Cholinesterase Inhibitors, Histamine
Male, Mice, Inbred ICR, Dose-Response Relationship, Drug, Nifedipine, Physostigmine, In Vitro Techniques, Phenylethyl Alcohol, Gastric Acid, Mice, Caffeic Acids, Gastrointestinal Agents, Gastric Mucosa, 1-Methyl-3-isobutylxanthine, Muscarine, Acetylcholinesterase, Potassium, Animals, Pentagastrin, Cholinesterase Inhibitors, Histamine
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