Localization of technetium‐99m diphosphonate in acutely injured muscle
- 1 March 1977
- journal article
- research article
- Published by Wolters Kluwer Health in Neurology
- Vol. 27 (3), 230
- https://doi.org/10.1212/wnl.27.3.230
Abstract
In rats with experimental ischemic myopathy, there was a significant correlation (r = 0.778, p < 0.001) between muscle uptake of techne tium-99m (99mTc) diphosphonate and tissue calcium concentration. In addition, the accumulation of both calcium and 99mTc-diphosphonate in acutely injured muscles was further increased in rats with vitamin D-induced hypercalcemia. Histologic studies demonstrated staining of damaged muscle fibers with alizarin red, indicating the presence of microcrystalline or ultramicrocrystalline calcium salts. Staining of muscle fibers was most intense in the outer marginal zones of individual microscopic infarcts. Our results suggest that the uptake of 99mTc-diphosphonate in acutely damaged skeletal muscle is directly related to the deposition of calcium salts within the injured muscle fibers.This publication has 9 references indexed in Scilit:
- AN IMPROVED PROCEDURE FOR SERUM CREATINE PHOSPHOKINASE DETERMINATION1967
- Reversal of the ATPase Reaction in Muscle Fibres By EDTANature, 1966
- MITOCHONDRIAL LOCALIZATION OF OXIDATIVE ENZYMES: STAINING RESULTS WITH TWO TETRAZOLIUM SALTSThe Journal of cell biology, 1961
- Histochemical Demonstration of Acid Phosphatases With Naphthol AS-PhosphatesJNCI Journal of the National Cancer Institute, 1958
- HISTOCHEMICAL METHODS FOR CALCIUMJournal of Histochemistry & Cytochemistry, 1958
- THE ACUTE CALCIFICATION OF TRAUMATIZED MUSCLE, WITH PARTICULAR REFERENCE TO ACUTE POST-TRAUMATIC RENAL INSUFFICIENCY 1Journal of Clinical Investigation, 1957
- DISTRIBUTION OF AMYLOPHOSPHORYLASE IN VARIOUS TISSUES OF HUMAN AND MAMMALIAN ORGANSJournal of Histochemistry & Cytochemistry, 1955
- THE SPECIFICITY OF THE HISTOCHEMICAL METHOD FOR ADENOSINE TRIPHOSPHATASJournal of Histochemistry & Cytochemistry, 1955
- The Histochemical Demonstration of Esterase2JNCI Journal of the National Cancer Institute, 1949