Comparison of osteopenia after gastrectomy, ovariectomy and prednisolone treatment in the young female rat

• Published in: Acta orthopaedica 2001, Vol.72 (5), p.525-532
• Main Authors: Surve, Vikas V, Andersson, Niklas, Lehto-Axtelius, Daisy, Håkanson, Rolf
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Bone Density; Bone Diseases, Metabolic - chemically induced; Bone Diseases, Metabolic - etiology; Bone Diseases, Metabolic - pathology; Disease Models, Animal; Femur - pathology; Fundamental and applied biological sciences. Psychology; Gastrectomy; Ovariectomy; Postoperative Complications; Prednisolone - therapeutic use; Rats; Rats, Sprague-Dawley; Skeleton and joints; Vertebrates: osteoarticular system, musculoskeletal system
• ISSN: 1745-3674; 0001-6470; 1745-3682
• DOI: 10.1080/000164701753532880

Rat models of osteopenia include ovariectomy and long-term glucocorticoid treatment. Although ovariectomy produces significant trabecular bone loss after 2 weeks, long-term glucocorticoid treatment has been reported to cause osteopenia in some studies but not in others. In the present 8-week-study, we compared the osteopenia associated with gastrectomy (GX) to that induced by ovariectomy (OVX) or prednisolone (PRE) treatment. Female Sprague-Dawley rats (10 weeks old) were subjected to GX, OVX, PRE treatment or SHAM operation. At the end of the study, calvariae, femurs and fifth lumbar vertebrae (L5) were collected and subjected to bone density measurement (femur and L5), transillumination (calvaria) and histomorphometry (calvaria and femur). Bone density was reduced in L5 and the distal femur in the OVX and GX groups, but not in the PRE group. Transillumination of the calvaria showed marked bone loss in the GX rats, but not in the other groups. Morphometric analysis of the femur revealed reduced trabecular bone volume, trabecular thickness, trabecular number and osteoclast number, but increased osteoclast surface (expressed as per cent of the trabecular bone surface covered by osteoclasts) in the GX and OVX rats. The PRE rats seemed unaffected. Cortical thickness was reduced in the GX rats, but not in the other groups. The findings indicate that GX induces osteopenia in, e.g., femur and vertebra of a magnitude similar to or greater than that induced by OVX, while at the same time inducing osteopenia in the calvaria. Although osteoclast activation seems to contribute, the precise mechanism underlying the GX-evoked osteopenia remains obscure.