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Characterization of bone turnover and energy metabolism in a rat model of primary and secondary osteoporosis.
Bauer, Natali B; Khassawna, Thaqif El; Goldmann, Fee; Stirn, Martina; Ledieu, David; Schlewitz, Gudrun; Govindarajan, Parameswari; Zahner, Daniel; Weisweiler, David; Schliefke, Nathalie; Böcker, Wolfgang; Schnettler, Reinhard; Heiss, Christian; Moritz, Andreas.
Afiliación
  • Bauer NB; Department of Veterinary Clinical Sciences, Clinical Pathology and Clinical Pathophysiology, Justus-Liebig University Giessen, Frankfurterstraße 126, 35392 Giessen, Germany. Electronic address: natali.bauer@vetmed.uni-giessen.de.
  • Khassawna TE; Laboratory of Experimental Trauma Surgery, Justus-Liebig-University of Giessen, KerkraderStrasse 9, 35392 Giessen, Germany.
  • Goldmann F; Department of Veterinary Clinical Sciences, Clinical Pathology and Clinical Pathophysiology, Justus-Liebig University Giessen, Frankfurterstraße 126, 35392 Giessen, Germany.
  • Stirn M; Translational Safety Biomarkers, PreClinical Safety, Novartis Institute for BioMedical Research, Novartis Pharma AG, WerkKlybeck, 4002 Basel, Switzerland.
  • Ledieu D; Translational Safety Biomarkers, PreClinical Safety, Novartis Institute for BioMedical Research, Novartis Pharma AG, WerkKlybeck, 4002 Basel, Switzerland.
  • Schlewitz G; Laboratory of Experimental Trauma Surgery, Justus-Liebig-University of Giessen, KerkraderStrasse 9, 35392 Giessen, Germany; Department of Trauma Surgery, University Hospital of Giessen-Marburg GmbH, Rudolf-Buchheim-Straße 7, 35385 Giessen, Germany.
  • Govindarajan P; Laboratory of Experimental Trauma Surgery, Justus-Liebig-University of Giessen, KerkraderStrasse 9, 35392 Giessen, Germany.
  • Zahner D; Animal Laboratory, Justus-Liebig University Giessen, Frankfurterstraße 105, 35392 Giessen, Germany.
  • Weisweiler D; Laboratory of Experimental Trauma Surgery, Justus-Liebig-University of Giessen, KerkraderStrasse 9, 35392 Giessen, Germany.
  • Schliefke N; Laboratory of Experimental Trauma Surgery, Justus-Liebig-University of Giessen, KerkraderStrasse 9, 35392 Giessen, Germany.
  • Böcker W; Laboratory of Experimental Trauma Surgery, Justus-Liebig-University of Giessen, KerkraderStrasse 9, 35392 Giessen, Germany; Department of Trauma Surgery, University Hospital of Giessen-Marburg GmbH, Rudolf-Buchheim-Straße 7, 35385 Giessen, Germany.
  • Schnettler R; Laboratory of Experimental Trauma Surgery, Justus-Liebig-University of Giessen, KerkraderStrasse 9, 35392 Giessen, Germany; Department of Trauma Surgery, University Hospital of Giessen-Marburg GmbH, Rudolf-Buchheim-Straße 7, 35385 Giessen, Germany.
  • Heiss C; Laboratory of Experimental Trauma Surgery, Justus-Liebig-University of Giessen, KerkraderStrasse 9, 35392 Giessen, Germany; Department of Trauma Surgery, University Hospital of Giessen-Marburg GmbH, Rudolf-Buchheim-Straße 7, 35385 Giessen, Germany.
  • Moritz A; Department of Veterinary Clinical Sciences, Clinical Pathology and Clinical Pathophysiology, Justus-Liebig University Giessen, Frankfurterstraße 126, 35392 Giessen, Germany.
Exp Toxicol Pathol ; 67(4): 287-96, 2015 Apr.
Article en En | MEDLINE | ID: mdl-25773704
ABSTRACT

BACKGROUND:

An experimental rat model served for evaluation of bone- and energy metabolism in early and late stages of osteoporosis. For the early stage, we hypothesized that bilateral ovariectomy (OVX)+multi-deficiency diet (OVXD; depletion of vitamin D, calcium, vitamin K, phosphorus) would induce increased bone turnover while the late stage would be characterized by enhanced bone catabolism. Obesity, insulin resistance and hyperleptinemia would be seen during the whole course of disease. Healthy female Sprague Dawley rats (n=41) aged 10 weeks were randomly assigned to sham and treatment groups and sacrificed at 3, 12, and 14 months after the study began.

RESULTS:

In the early phase, OVXD was associated with an increase in body weight, but not, however, in later stages. There was a decrease in bone mineral density and relative bone volume (BV/TV) as assessed by Dual Energy X-ray Absorptiometry and micro computed tomography that was most severe in the later stages of disease, indicating bone catabolism. Osteocalcin limiting bone formation was increased initially, whereas later stages (14 months) were characterized by elevated osteopontin, suggesting bone remodeling. Severe hyperparathyroidism was present during all stages of disease. Only the early phases of disease were characterized by hyperinsulinemia and increased adrenocorticotrophic stimulating hormone, whereas in the late stage hypoleptinemia rather than hyperleptinemia was seen.

CONCLUSION:

Markers of bone and energy metabolism reflected both an increased bone turn over and ongoing bone remodeling associated with initial hyperinsulinemia. Osteopontin and osteocalcin can be used to differentiate early and late stages of osteoporosis.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Osteoporosis / Remodelación Ósea / Metabolismo Energético Tipo de estudio: Etiology_studies Límite: Animals Idioma: En Revista: Exp Toxicol Pathol Asunto de la revista: PATOLOGIA / TOXICOLOGIA Año: 2015 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Osteoporosis / Remodelación Ósea / Metabolismo Energético Tipo de estudio: Etiology_studies Límite: Animals Idioma: En Revista: Exp Toxicol Pathol Asunto de la revista: PATOLOGIA / TOXICOLOGIA Año: 2015 Tipo del documento: Article