Nephrology Dialysis Transplantation, Vol 13, Issue 1 53-58, Copyright © 1998 by Oxford University Press
H de Valk, H van Rijn, J Wielder and H Koomans
Background: Lower plasma magnesium concentrations are
associated with clinical problems such as arrhythmias and hypertension.
Plasma magnesium concentration is tightly controlled by the kidney.
Modifying renal magnesium threshold may provide a means to increase the
plasma magnesium concentration. Since evidence has been presented that
potassium deficiency by itself may increase renal magnesium loss, the
hypothesis that elevating plasma potassium would result in an increase in
plasma magnesium concentration was tested in healthy volunteers.
Methods: Plasma potassium was raised in nine healthy
volunteers by oral administration of 20 mg amiloride daily during 3 weeks.
Magnesium metabolism was assessed before and after this period by plasma
levels, urinary magnesium excretion and fractional magnesium excretion, and
magnesium loading test (MLT). This MLT allows calculation of renal
retention of magnesium load. Results: Basal plasma
magnesium levels (0.84±0.07 vs
0.84±0.05 mmol/l) as well as urinary magnesium excretion
(4.37±1.73 vs 3.67±1.37
mmol/day) and erythrocyte magnesium levels (1.72±0.16
vs 1.76±0.14 mmol Mg/l red blood cells)
were similar before and on amiloride. Plasma potassium rose significantly
on amiloride (3.64±0.24 vs
4.07±0.54 mmol/l, P <0.05). No change was observed in
magnesium retention with the MLT: 22.7±26.7
vs 29.2±20.6% (P=0.5).
Conclusions: Despite an increased plasma potassium
concentration, no change was observed in plasma magnesium levels, urinary
magnesium excretion or renal magnesium retention of an intravenously
administered magnesium load. This indicates that increasing plasma
potassium within the normal range does not modify the renal magnesium
threshold. Key words: amiloride; magnesium; magnesium
loading test; potassium
ORIGINAL ARTICLES
Effect of an increase in the plasma potassium concentration on renal magnesium handling in healthy volunteers
Departments of Internal Medicine, Clinical Chemistry, and Nephrology, University Hospital, Utrecht, The Netherlands; Department of Clinical Chemistry, Eemland Hospital, Amersfoort, The Netherlands; Corresponding author at: Department of Internal Medicine, G02.228, Utrecht University Hospital, Heidelberglaan 100, 3584 CX, Utrecht, The Netherlands
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