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10.1007/BF02405119

http://scihub22266oqcxt.onion/10.1007/BF02405119
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6652550!ä!6652550

suck abstract from ncbi


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pmid6652550      Calcif+Tissue+Int 1983 ; 35 (6): 755-61
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  • Influence of magnesium supplementation on bone turnover in the normal young mouse #MMPMID6652550
  • Marie PJ; Travers R; Delvin EE
  • Calcif Tissue Int 1983[Sep]; 35 (6): 755-61 PMID6652550show ga
  • The effect of magnesium (Mg) supplementation on bone metabolism has been studied in the normal young mouse. Weanling male mice were given Mg-supplemented drinking water (5 mM or 32 mM Mg) for 4 weeks. Mineral and skeletal changes were assessed by biochemical methods and by histomorphometric analysis of endosteal bone formation and resorption parameters evaluated on tetracycline double-labeled, undecalcified caudal vertebrae. Magnesium supplementation increased serum and urinary Mg concentrations and bone Mg content. Both the calcification rate and the extent of tetracycline double-labeled osteoid surface increased progressively in Mg-treated mice, whereas the mineralization lag time was shortened. The osteoblastic surface was reduced, leading to a fall in osteoid surface. Stimulation of bone mineralization was associated with a rise in extracellular calcium (Ca) and phosphorus (P) concentrations whereas serum 25-OHD and 1,25(OH)2D levels remained normal. The Mg supplementation increased the number of acid phosphatase stained chondroclasts and osteoclasts and the extent of resorbing surface showing histochemically stained osteoclasts. Although urinary OH-proline increased above normal, Ca, P, and cyclic adenylic acid (cAMP) excretion and phosphate concentration (TmP/GFR) remained normal, suggesting that parathyroid hormone (PTH) secretion was not altered. The trabecular bone volume remained normal, showing that the increased bone resorption was balanced by the stimulated bone mineralization. The results show that Mg supplementation influenced both bone formation and resorption in the young mouse, and that the stimulation of bone mineralization was the result of increased extracellular mineral availability.(ABSTRACT TRUNCATED AT 250 WORDS)
  • |Animals[MESH]
  • |Bone Resorption/drug effects[MESH]
  • |Bone and Bones/cytology/*physiology[MESH]
  • |Calcification, Physiologic[MESH]
  • |Calcium/metabolism[MESH]
  • |Magnesium/*administration & dosage/metabolism[MESH]
  • |Male[MESH]
  • |Mice[MESH]
  • |Mice, Inbred C57BL[MESH]
  • |Osteoclasts/cytology[MESH]
  • |Osteogenesis/drug effects[MESH]


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