Artigo Acesso aberto Revisado por pares

Evaluation of hematology, general serum biochemistry, bone turnover markers and bone marrow cytology in a glucocorticoid treated ovariectomized sheep model for osteoporosis research

2020; Brazilian Academy of Sciences; Volume: 92; Issue: 4 Linguagem: Inglês

10.1590/0001-3765202020200435

ISSN

1678-2690

Autores

CATARINA A. COELHO, JOÃO P. BORDELO, José Arthur de Abreu Camassa, VERA A. BARROS, Pedro S. Babo, Manuela E. Gomes, Rui L. Reis, Jorge Manuel Teixeira de Azevedo, João Requicha, Pedro Faísca, Pedro P. Carvalho, Carlos Viegas, Isabel R. Dias,

Tópico(s)

Bone health and treatments

Resumo

Osteoporosis is a metabolic disorder characterized by a loss of bone mass and structure and increasing the risk of fragility fractures, mostly among postmenopausal women. Sheep is a recognized large animal model for osteoporosis research. An experimental group of ewes (3-4 years old) was subjected to ovariectomy (OVX) and weekly glucocorticoid (GC) application for 24 weeks and compared with a sham control group. Blood and bone marrow parameters were analyzed before and 24 weeks after OVX and GC administration. Osteopenia was confirmed through micro-computed tomography and histomorphometric analysis of L4 vertebra in the study end. A statistically significant increase was observed in mean corpuscular volume, mean cell hemoglobin and monocytes and a decrease in red blood count and eosinophils (p<0.05). Alkaline phosphatase (ALP), gamma-glutamyl transpeptidase, magnesium and α1-globulin increased, and creatinine, albumin, sodium and estradiol decreased (p<0.05). A slight decrease of bone formation markers (bone ALP and osteocalcin) and an increase of bone resorption markers (C-terminal telopeptides of collagen type 1 and tartrate-resistant acid phosphatase) were observed, but without statistical significance. This study aims to contribute to better knowledge of sheep as a model for osteoporosis research and the consequences that a performed induction protocol may impose on organic metabolism.

Referência(s)