Abstract

Caffeine is known to stimulate gastric acid secretion, but, the effects of caffeine on gastric mucus secretion have not been clarified. To elucidate the action of caffeine on gastric mucin-producing cells and its underlying mechanism, the effects of caffeine on mucus glycoprotein secretion and agonist-induced [Ca 2+] i mobilization were examined in human gastric mucin secreting cells (JR-I cells). The measurement of [Ca 2+] i using Indo-1 and the whole cell voltage clamp technique were applied. Mucus glycoprotein secretion was assessed by release of [ 3H]glucosamine. Caffeine by itself failed to increase [Ca 2+] i and affect membrane currents, while it dose-dependently inhibited agonist (acetylcholine (ACh) or histamine)-induced [Ca 2+] i rise, resulting in inhibiting activation of Ca 2+-dependent K + current (I K.Ca) evoked by agonists. The effect of caffeine was reversible, and the half maximal inhibitory concentration was about 0.5 mM. But, caffeine did not suppress [Ca 2+] i rise and activation of I K.Ca induced by A23187 or inositol trisphosphate (IP 3). Theophylline or 3-isobutyl-1-methyl-xanthine (IBMX) did not mimic the effect of caffeine. Caffeine failed to stimulate mucus secretion, while it significantly decreased ACh-induced mucus secretion. These results indicate that caffeine selectively inhibits agonist-mediated [Ca 2+] i rise in human gastric epithelial cells, probably through the blockade of receptor-IP 3 signaling pathway, which may affect the mucin secretion. © 1997 Elsevier Science B.V. All rights reserved.

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