Narongrit ThongonNateetip KrishnamraBurapha UniversityMahidol University2018-05-032018-05-032011-03-28World Journal of Gastroenterology. Vol.17, No.12 (2011), 1574-1583100793272-s2.0-79955934886https://repository.li.mahidol.ac.th/handle/20.500.14594/12585AIM: To elucidate the effect and underlying mechanisms of omeprazole action on Mg 2+ transport across the intestinal epithelium. METHODS: Caco-2 monolayers were cultured in various dose omeprazole-containing media for 14 or 21 d before being inserted into a modified Ussing chamber apparatus to investigate the bi-directional Mg 2+ transport and electrical parameters. Paracellular permeability of the monolayer was also observed by the dilution potential technique and a cation permeability study. An Arrhenius plot was performed to elucidate the activation energy of passive Mg 2+ transport across the Caco-2 monolayers. RESULTS: Both apical to basolateral and basolateral to apical passive Mg 2+ fluxes of omeprazole-treated epithelium were decreased in a dose- and time-dependent manner. Omeprazole also decreased the paracellular cation selectivity and changed the paracellular selective permeability profile of Caco-2 epithelium to Li + , Na + , K + , Rb + , and Cs + from series VII to series VI of the Eisenman sequence. The Arrhenius plot revealed the higher activation energy for passive Mg 2+ transport in omeprazole treated epithelium than that of control epithelium, indicating that omeprazole affected the paracellular channel of Caco-2 epithelium in such a way that Mg 2+ movement was impeded. CONCLUSION: Omeprazole decreased paracellular cation permeability and increased the activation energy for passive Mg 2+ transport of Caco-2 monolayers that led to the suppression of passive Mg 2+ absorption. © 2011 Baishideng. All rights received.Mahidol UniversityMedicineArticleSCOPUS10.3748/wjg.v17.i12.1574