Magnesium and Calcium Transport along the Male Rat Kidney: Effect of Diuretics

Author:

Dutta Pritha1ORCID,Layton Anita T.1234

Affiliation:

1. Department of Applied Mathematics, University of Waterloo, Waterloo, ON N2L 3G1, Canada

2. Cheriton School of Computer Science, University of Waterloo, Waterloo, ON N2L 3G1, Canada

3. Department of Biology, University of Waterloo, Waterloo, ON N2L 3G1, Canada

4. School of Pharmacy, University of Waterloo, Waterloo, ON N2L 3G1, Canada

Abstract

Calcium (Ca2+) and magnesium (Mg2+) are essential for cellular function. The kidneys play an important role in maintaining the homeostasis of these cations. Their reabsorption along the nephron is dependent on distinct trans- and paracellular pathways and is coupled to the transport of other electrolytes. Notably, sodium (Na+) transport establishes an electrochemical gradient to drive Ca2+ and Mg2+ reabsorption. Consequently, alterations in renal Na+ handling, under pathophysiological conditions or pharmacological manipulations, can have major effects on Ca2+ and Mg2+ transport. One such condition is the administration of diuretics, which are used to treat a large range of clinical conditions, but most commonly for the management of blood pressure and fluid balance. While the pharmacological targets of diuretics typically directly mediate Na+ transport, they also indirectly affect renal Ca2+ and Mg2+ handling through alterations in the electrochemical gradient. To investigate renal Ca2+ and Mg2 handling and how those processes are affected by diuretic treatment, we have developed computational models of electrolyte transport along the nephrons. Model simulations indicate that along the proximal tubule and thick ascending limb, the transport of Ca2+ and Mg2+ occurs in parallel with Na+, but those processes are dissociated along the distal convoluted tubule. We also simulated the effects of acute administration of loop, thiazide, and K-sparing diuretics. The model predicted significantly increased Ca2+ and Mg2+ excretions and significantly decreased Ca2+ and Mg2+ excretions on treatment with loop and K-sparing diuretics, respectively. Treatment with thiazide diuretics significantly decreased Ca2+ excretion, but there was no significant alteration in Mg2+ excretion. The present models can be used to conduct in silico studies on how the kidney adapts to alterations in Ca2+ and Mg2+ homeostasis during various physiological and pathophysiological conditions, such as pregnancy, diabetes, and chronic kidney disease.

Funder

Canada 150 Research Chair program

Canada Institutes of Health Research

Publisher

MDPI AG

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