Propranolol attenuates risperidone-induced trabecular bone loss in female mice.

Document Type

Article

Publication Date

7-1-2015

Institution/Department

Translational Research; MMCRI

Journal Title

Endocrinology

MeSH Headings

Adipose Tissue, Brown, Adrenergic beta-Antagonists, Animals, Antipsychotic Agents, Bone Diseases, Metabolic, Bone Remodeling, Bone and Bones, Energy Metabolism, Female, Ion Channels, Mice, Mice, Knockout, Mitochondrial Proteins, Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha, Propranolol, RANK Ligand, Receptors, Adrenergic, beta-2, Risperidone, Sympathetic Nervous System, Thermogenesis, Transcription Factors, Uncoupling Protein 1

Abstract

Atypical antipsychotic (AA) drugs cause significant metabolic side effects, and clinical data are emerging that demonstrate increased fracture risk and bone loss after treatment with the AA, risperidone (RIS). The pharmacology underlying the adverse effects on bone is unknown. However, RIS action in the central nervous system could be responsible because the sympathetic nervous system (SNS) is known to uncouple bone remodeling. RIS treatment in mice significantly lowered trabecular bone volume fraction (bone volume/total volume), owing to increased osteoclast-mediated erosion and reduced osteoblast-mediated bone formation. Daytime energy expenditure was also increased and was temporally associated with the plasma concentration of RIS. Even a single dose of RIS transiently elevated expression of brown adipose tissue markers of SNS activity and thermogenesis, Pgc1a and Ucp1. Rankl, an osteoclast recruitment factor regulated by the SNS, was also increased 1 hour after a single dose of RIS. Thus, we inferred that bone loss from RIS was regulated, at least in part, by the SNS. To test this, we administered RIS or vehicle to mice that were also receiving the nonselective β-blocker propranolol. Strikingly, RIS did not cause any changes in trabecular bone volume/total volume, erosion, or formation while propranolol was present. Furthermore, β2-adrenergic receptor null (Adrb2(-/-)) mice were also protected from RIS-induced bone loss. This is the first report to demonstrate SNS-mediated bone loss from any AA. Because AA medications are widely prescribed, especially to young adults, clinical studies are needed to assess whether β-blockers will prevent bone loss in this vulnerable population.

ISSN

1945-7170

First Page

2374

Last Page

2383

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