Abstract
Inorganic phosphate (Pi), pyrophosphate (PPi) and its synthetic analogues, dichloromethanediphosphonate (Cl2MDP) and 1-hydroxyethane-1, 1-diphosphonate (EHDP) compete for sites in bone mineral affecting the formation and dissolution of apatite.1 The diphosphonates may also affect the metabolism of bone and cartilage cells and possibly other tissues by interacting with enzymes or proteins which bind phosphate or phosphorylated intermediates. Available data indicate that Cl2MDP increases the production of CO2 from acetate, leucine, citrate and palmitate; stimulates the synthesis of collagen, proteoglycans and glycogen; increases alkaline phosphatase activity and inhibits lactate formation in cultured calvaria cells.2,3
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© 1984 Plenum Press, New York
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Biltz, R.M., Pellegrino, E.D., Letteri, J.M., Pinkus, L.M. (1984). Inorganic Phosphate, Pyrophosphate and the Diphosphonates Activate Bone (Calvaria) Glutaminase. In: Massry, S.G., Maschio, G., Ritz, E. (eds) Phosphate and Mineral Metabolism. Advances in Experimental Medicine and Biology, vol 178. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-4808-5_30
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DOI: https://doi.org/10.1007/978-1-4684-4808-5_30
Publisher Name: Springer, Boston, MA
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