Decrease in particle-induced osteolysis in obese (ob/ob) mice

There may be variability in the susceptibility of different individuals to osteolysis from wear debris, and it is not clear whether some individuals may have a genetic predisposition for a more marked osteolytic response. The purpose of this study in mice was to determine whether genetically determi...

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Published inBiomaterials Vol. 25; no. 19; pp. 4675 - 4681
Main Authors von Knoch, M., Jewison, D.E., Sibonga, J.D., Turner, R.T., Morrey, B.F., Loer, F., Berry, D.J., Scully, S.P.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier Ltd 01.08.2004
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Summary:There may be variability in the susceptibility of different individuals to osteolysis from wear debris, and it is not clear whether some individuals may have a genetic predisposition for a more marked osteolytic response. The purpose of this study in mice was to determine whether genetically determined obesity can alter the response to particulate debris. Polyethylene particles were implanted onto the calvaria of seven wild-type mice and seven obese mice (ob/ob). Calvaria from unimplanted wild-type and obese mice served as controls. Calvaria were harvested after 7 days, stained with toluidine blue and for tartrate-specific alkaline phosphatase, and analyzed by histomorphometry. The osteoclast number per mm total bone perimeter was 8.000±3.464 in wild-type animals with particles and 2.857±1.676 in ob/ob animals with particles ( p=0.0002; Fisher's PLSD). Bone resorption was 1.895±0.713 mm/mm 2 in wild-type animals with particles and 1.265±0.494 mm/mm 2 in ob/ob animals with particles ( p=0.0438; Fisher's PLSD). Particles induced a diminished osteolytic response in genetically determined obese mice, suggesting that obesity may have a protective role against particle-induced bone resorption—similar to obesity and osteoporosis. These important new findings may help to stimulate clinical studies which may define criteria to better identify patients at risk to develop particle-induced osteolysis.
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ISSN:0142-9612
1878-5905
DOI:10.1016/j.biomaterials.2004.02.069