Department of Physiology, Radboud University Medical Center, Nijmegen, The Netherlands;
School of Medicine, University of Tampere, Tampere, Finland; Department of Internal Medicine, Tampere University Hospital, Tampere, Finland;
Am J Physiol Gastrointest Liver Physiol. 2015 Feb 1;308(3):G206-16. doi: 10.1152/ajpgi.00093.2014. Epub 2014 Dec 4.
Calcium (Ca(2+)) and magnesium (Mg(2+)) ions are involved in many vital physiological functions. Since dietary intake is the only source of minerals for the body, intestinal absorption is essential for normal homeostatic levels. The aim of this study was to characterize the absorption of Ca(2+) as well as Mg(2+) along the gastrointestinal tract at a molecular and functional level. In both humans and mice the Ca(2+) channel transient receptor potential vanilloid subtype 6 (TRPV6) is expressed in the proximal intestinal segments, whereas Mg(2+) channel transient receptor potential melastatin subtype 6 (TRPM6) is expressed in the distal parts of the intestine. A method was established to measure the rate of Mg(2+) absorption from the intestine in a time-dependent manner by use of (25)Mg(2+). In addition, local absorption of Ca(2+) and Mg(2+) in different segments of the intestine of mice was determined by using surgically implanted intestinal cannulas. By these methods, it was demonstrated that intestinal absorption of Mg(2+) is regulated by dietary needs in a vitamin D-independent manner. Also, it was shown that at low luminal concentrations, favoring transcellular absorption, Ca(2+) transport mainly takes place in the proximal segments of the intestine, whereas Mg(2+) absorption predominantly occurs in the distal part of the gastrointestinal tract. Vitamin D treatment of mice increased serum Mg(2+) levels and 24-h urinary Mg(2+) excretion, but not intestinal absorption of (25)Mg(2+). Segmental cannulation of the intestine and time-dependent absorption studies using (25)Mg(2+) provide new ways to study intestinal Mg(2+) absorption.
钙(Ca(2+))和镁(Mg(2+))离子参与许多重要的生理功能。由于饮食摄入是身体矿物质的唯一来源,因此肠道吸收对于正常的体内平衡水平至关重要。本研究的目的是从分子和功能水平上描述 Ca(2+)以及 Mg(2+)在胃肠道中的吸收。在人和小鼠中,钙通道瞬时受体电位香草酸亚型 6(TRPV6)在肠道的近端节段表达,而镁通道瞬时受体电位 melastatin 亚型 6(TRPM6)在肠道的远端部分表达。建立了一种方法,通过使用(25)Mg(2+),以时间依赖性方式测量从肠道吸收 Mg(2+)的速率。此外,通过使用手术植入的肠道套管,确定了不同肠道段中 Ca(2+)和 Mg(2+)的局部吸收。通过这些方法,证明了 Mg(2+)的肠道吸收受维生素 D 独立的饮食需求调节。此外,还表明在低腔浓度下,有利于细胞旁吸收,Ca(2+)转运主要发生在肠道的近端段,而 Mg(2+)吸收主要发生在胃肠道的远端部分。用维生素 D 处理小鼠会增加血清 Mg(2+)水平和 24 小时尿 Mg(2+)排泄,但不会增加(25)Mg(2+)的肠道吸收。肠道的分段套管和使用(25)Mg(2+)的时间依赖性吸收研究为研究肠道 Mg(2+)吸收提供了新的方法。