Exp Mol Med.  2012 Nov;44(11):684-693.

Apical acidity decreases inhibitory effect of omeprazole on Mg2+ absorption and claudin-7 and -12 expression in Caco-2 monolayers

Affiliations
  • 1Faculty of Allied Health Sciences, Burapha University, Chonburi 20131, Thailand. narongritt@buu.ac.th
  • 2Consortium for Calcium and Bone Research (COCAB), Faculty of Science, Mahidol University, Bangkok 10400, Thailand.
  • 3Department of Physiology, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.

Abstract

Clinical studies reported hypomagnesaemia in long-term omeprazole usage that was probably due to intestinal Mg2+ wasting. Our previous report demonstrated the inhibitory effect of omeprazole on passive Mg2+ transport across Caco-2 monolayers. The present study aimed to identify the underlying mechanism of omeprazole suppression of passive Mg2+ absorption. By using Caco-2 monolayers, we demonstrated a potent inhibitory effect of omeprazole on passive Mg2+, but not Ca2+, transport across Caco-2 monolayers. Omeprazole shifted the %maximum passive Mg2+ transport-Mg2+ concentration curves to the right, and increased the half maximal effective concentration of those dose-response curves, indicating a lower Mg2+ affinity of the paracellular channel. By continually monitoring the apical pH, we showed that omeprazole suppressed apical acid accumulation. Neomycin and spermine had no effect on passive Mg2+ transport of either control or omeprazole treated monolayers, indicating that omeprazole suppressed passive Mg2+ transport in a calcium sensing receptor (CaSR)-independent manner. The results of western blot analysis showed that omeprazole significantly suppressed claudin (Cldn)-7 and -12, but not Cldn-2, expression in Caco-2 cells. By using apical solution of pH 5.5, 6.0, 6.5, and 7.0, we found that apical acidity markedly increased passive Mg2+ transport, Mg2+ affinity of the paracellular channel, and Cldn-7 and -12 expression in Caco-2 monolayers. Apical acidity abolished the inhibitory effect of omeprazole on passive Mg2+ transport and Cldn-7 and -12 expression. Our results provided the evidence for the regulation of intestinal passive Mg2+ absorption by luminal acidity-induced increase in Cldn-7 and -12 expression.

Keyword

claudins; intestines; magnesium; omeprazole; proton pump inhibitors; tight junctions

MeSH Terms

Absorption/drug effects
Caco-2 Cells
Calcium/metabolism
Claudins/genetics/*metabolism
Dose-Response Relationship, Drug
Gene Expression/drug effects
Humans
Hydrogen-Ion Concentration
Magnesium/*metabolism
Omeprazole/*pharmacology
Proton Pump Inhibitors/*pharmacology
Receptors, Calcium-Sensing/metabolism
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