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奥美拉唑可降低 Caco-2 单层细胞对镁的转运。

Omeprazole decreases magnesium transport across Caco-2 monolayers.

机构信息

Faculty of Allied Health Sciences, Burapha University, Chonburi 20131, Thailand.

出版信息

World J Gastroenterol. 2011 Mar 28;17(12):1574-83. doi: 10.3748/wjg.v17.i12.1574.

Abstract

AIM

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.

摘要

目的

阐明奥美拉唑对肠上皮细胞镁(Mg2+)转运的作用及其机制。

方法

用含不同浓度奥美拉唑的培养液培养 Caco-2 单层细胞 14 或 21 天后,将其插入改良的 Ussing 室装置,研究双向镁(Mg2+)转运和电参数。还通过稀释电位技术和阳离子通透性研究观察单层细胞的旁道通透性。通过阿仑尼乌斯图阐明被动跨 Caco-2 单层细胞的镁(Mg2+)转运的活化能。

结果

奥美拉唑处理的上皮细胞中,镁(Mg2+)从顶侧向基底侧和从基底侧向顶侧的被动转运均呈剂量和时间依赖性下降。奥美拉唑还降低了细胞旁阳离子选择性,并改变了 Caco-2 上皮细胞的细胞旁选择性通透性谱,使 Li(+)、Na(+)、K(+)、Rb(+)和 Cs(+)从 Eisenman 序列的 VII 系列变为 VI 系列。阿仑尼乌斯图显示,奥美拉唑处理的上皮细胞中镁(Mg2+)的被动转运的活化能高于对照上皮细胞,表明奥美拉唑以某种方式影响了 Caco-2 上皮细胞的细胞旁通道,从而阻碍了镁(Mg2+)的运动。

结论

奥美拉唑降低了细胞旁阳离子通透性,增加了 Caco-2 单层细胞的镁(Mg2+)被动转运的活化能,从而抑制了镁(Mg2+)的被动吸收。

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