Osteoprotective effect of propranolol in ovariectomized rats: a comparison with zoledronic acid and alfacalcidol

• Published in: Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association 2013-09, Vol.18 (5), p.832-842
• Main Authors: Khajuria, Deepak Kumar, Razdan, Rema, Mahapatra, D. Roy, Bhat, M.R.
• Format: Article
• Language: English
• Subjects: Adrenergic beta-Antagonists - therapeutic use; Animals; Bone Density Conservation Agents - therapeutic use; Diphosphonates - therapeutic use; Female; Hydroxycholecalciferols - therapeutic use; Imidazoles - therapeutic use; Medicine; Medicine & Public Health; Original Article; Orthopedics; Osteoporosis - etiology; Osteoporosis - prevention & control; Ovariectomy; Propranolol - therapeutic use; Rats; Rats, Wistar; Rheumatology
• ISSN: 0949-2658; 1436-2023
• DOI: 10.1007/s00776-013-0433-y

Currently β-adrenergic receptor blockers are considered to be potential drugs under investigation for preventive or therapeutic effect in osteoporosis. However, there is no published data showing the comparative study of β-blockers with well accepted agents for the treatment of osteoporosis. To address this question, we compared the effects of propranolol with well accepted treatments like zoledronic acid and alfacalcidol in an animal model of postmenopausal osteoporosis. Five days after ovariectomy, 36 ovariectomized (OVX) rats were divided into 6 equal groups, randomized to treatments zoledronic acid (100μg/kg, intravenous single dose); alfacalcidol (0.5μg/kg, oral gauge daily); propranolol (0.1mg/kg, subcutaneously 5days per week) for 12weeks. Untreated OVX and sham OVX were used as controls. At the end of treatment serum calcium and alkaline phosphatase were assayed. Femurs were removed and tested for bone density, bone porosity, bone mechanical properties and trabecular micro-architecture. Propranolol showed a significant decrease in alkaline phosphatase levels and bone porosity in comparison to OVX control. Moreover, propranolol significantly improved bone density, bone mechanical properties and inhibited the deterioration of trabecular microarchitecture when compared with OVX control. The osteoprotective effect of propranolol was comparable with zoledronic acid and alfacalcidol. Based on this comparative study, the results strongly suggest that propranolol can be a candidate therapeutic drug for the management of postmenopausal osteoporosis.