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10.1684/mrh.2015.0394

http://scihub22266oqcxt.onion/10.1684/mrh.2015.0394
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26878252!ä!26878252

suck abstract from ncbi


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pmid26878252      Magnes+Res 2015 ; 28 (4): 126-35
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  • Hyperphosphatemia, hypocalcemia and increased serum potassium concentration as distinctive features of early hypomagnesemia in magnesium-deprived mice #MMPMID26878252
  • Ortega B; MacWilliams JR; Dey JM; Courtright VB
  • Magnes Res 2015[Dec]; 28 (4): 126-35 PMID26878252show ga
  • Magnesium-deficient patients show dysfunctional calcium (Ca(2+)) metabolism due to defective parathyroid hormone (PTH) secretion. In mice and rats, long-term magnesium (Mg(2+)) deprivation causes hyperphosphaturia and increases fibroblast growth factor 23 (FGF23) secretion, despite normal serum phosphate (Pi) and Ca(2+). Electrolyte disturbances during early hypomagnesemia may explain the response of mice to long-term Mg(2+) deprivation, but our knowledge of electrolyte homeostasis during this stage is limited. This study compares the effect of both short- and long-term Mg(2+) restriction on the electrolyte balance in mice. Mice were fed control or Mg(2+)-deficient diets for one to three days, one week, or three weeks. Prior to killing the mice, urine was collected over 24 h using metabolic cages. Within 24 h of Mg(2+) deprivation, hypomagnesemia, hypocalcemia and hyperphosphatemia developed, and after three days of Mg(2+) deprivation, serum potassium (K(+)) was increased. These changes were accompanied by a reduction in urinary volume, hyperphosphaturia, hypocalciuria and decreased Mg(2+), sodium (Na(+)) and K(+) excretion. Surprisingly, after one week of Mg(2+) deprivation, serum K(+), Pi and Ca(2+) had normalized, showing that mineral homeostasis is most affected during early hypomagnesemia. Serum Pi and K(+) are known to stimulate secretion of FGF23 and aldosterone, which are usually elevated during Mg(2+) deficiency. Thus, the hyperphosphatemia and increased serum K(+) concentration observed during short-term Mg(2+) deprivation may help our understanding of adaptation to chronic Mg(2+) deficiency.
  • |Adaptation, Physiological[MESH]
  • |Animals[MESH]
  • |Biomarkers/blood/urine[MESH]
  • |Body Weight[MESH]
  • |Calcium/*blood/urine[MESH]
  • |Disease Models, Animal[MESH]
  • |Fibroblast Growth Factor-23[MESH]
  • |Hyperkalemia/blood/*etiology/physiopathology/urine[MESH]
  • |Hyperphosphatemia/blood/*etiology/physiopathology/urine[MESH]
  • |Hypocalcemia/blood/*etiology/physiopathology/urine[MESH]
  • |Magnesium Deficiency/blood/*complications/physiopathology/urine[MESH]
  • |Magnesium/*blood/urine[MESH]
  • |Male[MESH]
  • |Mice, Inbred C57BL[MESH]
  • |Phosphates/*blood/urine[MESH]
  • |Potassium/*blood/urine[MESH]
  • |Time Factors[MESH]


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