Renal calcium and magnesium handling during pregnancy: modeling and analysis.

Shervin Hakimi, Pritha Dutta, Anita T Layton
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Abstract

Pregnancy is associated with elevated demand of most nutrients, with many trace elements and minerals critical for the development of fetus. In particular, calcium (Ca2+) and magnesium (Mg2+) are essential for cellular function, and their deficiency can lead to impaired fetal growth. A key contributor to the homeostasis of these ions is the kidney, which in a pregnant rat undergoes major changes in morphology, hemodynamics, and molecular structure. The goal of this study is to unravel the functional implications of these pregnancy-induced changes in renal handling of Ca2+ and Mg2+, two cations that are essential in a healthy pregnancy. To achieve that goal, we developed computational models of electrolyte and water transport along the nephrons of a rat in mid and late pregnancy. Model simulations reveal a substantial increase in the reabsorption of Mg2+ along the proximal tubules and thick ascending limbs. In contrast, the reabsorption of Ca2+ is increased in the proximal tubules but decreased in the thick ascending limbs, due to the lower transepithelial concentration gradient of Ca2+ along the latter. Despite the enhanced transport capacity, the marked increase in glomerular filtration rate results in elevated urinary excretions of Ca2+ and Mg2+ in pregnancy. Furthermore, we conducted simulations of hypocalcemia and hypomagnesemia. We found that hypocalcemia lowers Ca2+ excretion substantially more than Mg2+ excretion, with this effect being more pronounced in virgin rats than in pregnant ones. Conversely, hypomagnesemia reduces the excretion of Mg2+ and Ca2+ to more similar degrees. These differences can be explained by the greater sensitivity of the calcium-sensing receptor (CaSR) to Ca2+ compared with Mg2+.NEW & NOTEWORTHY A growing fetus' demands of minerals, notably calcium and magnesium, necessitate adaptations in pregnancy. In particular, the kidney undergoes major changes in morphology, hemodynamics, and molecular structure. This computational modeling study provides insights into how these pregnancy-induced renal adaptation impact calcium and magnesium transport along different nephron segments. Model simulations indicate that, despite the enhanced transport capacity, the marked increase in glomerular filtration rate results in elevated urinary excretions of calcium and magnesium in pregnancy.

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妊娠期肾脏钙和镁的处理:建模与分析
妊娠期对大多数营养素的需求都会增加,其中许多微量元素和矿物质对胎儿的发育至关重要。其中,钙(Ca2+)和镁(Mg2+)对细胞功能至关重要,它们的缺乏会导致胎儿发育受损。对这些离子的平衡起关键作用的是肾脏,怀孕大鼠的肾脏在形态、血液动力学和分子结构方面都发生了重大变化。本研究的目的是揭示妊娠引起的这些变化对肾脏处理 Ca2+ 和 Mg2+ 的功能影响。我们建立了妊娠中期和晚期大鼠肾小球电解质和水转运的计算模型。模型模拟显示,近端肾小管和粗升支对 Mg2+ 的重吸收量大幅增加。相比之下,近端肾小管对 Ca2+ 的重吸收增加,但粗升支对 Ca2+ 的重吸收减少,原因是粗升支的 Ca2+ 经上皮浓度梯度较低。尽管运输能力增强,但肾小球滤过率的显著增加导致妊娠期尿液中 Ca2+ 和 Mg2+ 的排泄量增加。此外,我们还模拟了低钙血症和低镁血症。我们发现,低钙血症降低 Ca2+排泄量的程度远远高于降低 Mg2+排泄量的程度,尤其是对处女鼠而言。相反,低镁血症减少 Mg2+ 和 Ca2+ 排泄的程度较为相似。与 Mg2+ 相比,钙感应受体(CaSR)对 Ca2+ 的敏感性更高,这可以解释这些差异。
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