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Calcitonin substitution in calcitonin deficiency reduces particle-induced osteolysis

Authors :
Laura Neuerburg
Florian Grabellus
Martina Broecker-Preuss
Gero Hilken
Max Daniel Kauther
Christian Wedemeyer
Marius von Knoch
Hagen S. Bachmann
Gabriele Koehler
Source :
BMC Musculoskeletal Disorders, Vol 12, Iss 1, p 186 (2011), BMC Musculoskeletal Disorders
Publication Year :
2011
Publisher :
Springer Science and Business Media LLC, 2011.

Abstract

Background Periprosthetic osteolysis is a major cause of aseptic loosening in joint arthroplasty. This study investigates the impact of CT (calcitonin) deficiency and CT substitution under in-vivo circumstances on particle-induced osteolysis in Calca -/- mice. Methods We used the murine calvarial osteolysis model based on ultra-high molecular weight polyethylene (UHMWPE) particles in 10 C57BL/6J wild-type (WT) mice and twenty Calca -/- mice. The mice were divided into six groups: WT without UHMWPE particles (Group 1), WT with UHMWPE particles (Group 2), Calca -/- mice without UHMWPE particles (Group 3), Calca -/- mice with UHMWPE particles (Group 4), Calca -/- mice without UHMWPE particles and calcitonin substitution (Group 5), and Calca -/- mice with UHMWPE particle implantation and calcitonin substitution (Group 6). Analytes were extracted from serum and urine. Bone resorption was measured by bone histomorphometry. The number of osteoclasts was determined by counting the tartrate-resistant acid phosphatase (TRACP) + cells. Results Bone resorption was significantly increased in Calca -/- mice compared with their corresponding WT. The eroded surface in Calca -/- mice with particle implantation was reduced by 20.6% after CT substitution. Osteoclast numbers were significantly increased in Calca -/- mice after particle implantation. Serum OPG (osteoprotegerin) increased significantly after CT substitution. Conclusions As anticipated, Calca -/- mice show extensive osteolysis compared with wild-type mice, and CT substitution reduces particle-induced osteolysis.

Details

ISSN :
14712474
Volume :
12
Database :
OpenAIRE
Journal :
BMC Musculoskeletal Disorders
Accession number :
edsair.doi.dedup.....637460aacd7033b06a41654ae92dd494