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Treatment with soluble activin type IIB-receptor improves bone mass and strength in a mouse model of Duchenne muscular dystrophy

By Tero Puolakkainen, Hongqian Ma, Heikki Kainulainen, Arja Pasternack, Timo Rantalainen, Olli Ritvos, Kristiina Heikinheimo, Juha Hulmi and Riku Kiviranta

Abstract

Background: Inhibition of activin/myostatin pathway has emerged as a novel approach to increase muscle mass and bone strength. Duchenne muscular dystrophy (DMD) is a neuromuscular disorder that leads to progressive muscle degeneration and also high incidence of fractures. The aim of our study was to test whether inhibition of activin receptor IIB ligands with or without exercise could improve bone strength in the mdx mouse model for DMD. Methods: Thirty-two mdx mice were divided to running and non-running groups and to receive either PBS control or soluble activin type IIB-receptor (ActRIIB-Fc) once weekly for 7 weeks. Results: Treatment of mdx mice with ActRIIB-Fc resulted in significantly increased body and muscle weights in both sedentary and exercising mice. Femoral mu CT analysis showed increased bone volume and trabecular number (BV/TV +80%, Tb.N +70%, P <0.05) in both ActRIIB-Fc treated groups. Running also resulted in increased bone volume and trabecular number in PBS-treatedmice. However, there was no significant difference in trabecular bone structure or volumetric bone mineral density between the ActRIIB-Fc and ActRIIB-Fc-R indicating that running did not further improve bone structure in ActRIIB-Fc-treated mice. ActRIIB-Fc increased bone mass also in vertebrae (BV/TV +20%, Tb.N +30%, P <0.05) but the effects were more modest. The number of osteoclasts was decreased in histological analysis and the expression of several osteoblast marker genes was increased in ActRIIB-Fc treated mice suggesting decreased bone resorption and increased bone formation in these mice. Increased bone mass in femurs translated into enhanced bone strength in biomechanical testing as the maximum force and stiffness were significantly elevated in ActRIIB-Fc-treated mice. Conclusions: Our results indicate that treatment of mdx mice with the soluble ActRIIB-Fc results in a robust increase in bone mass, without any additive effect by voluntary running. Thus ActRIIB-Fc could be an attractive option in the treatment of musculoskeletal disorders

Topics: Bone mu CT, Bone-muscle interactions, TGF-beta s, Animal models, Exercise, MUSCLE PROTEIN-SYNTHESIS, MDX MICE, OXIDATIVE CAPACITY, MYOSTATIN, EXERCISE, DENSITY, METAANALYSIS, DEFICIENCY, PREVENTS, BLOCKING, 3126 Surgery, anesthesiology, intensive care, radiology, 3121 Internal medicine, Bone mu CT, Bone-muscle interactions, TGF-beta s, Animal models, Exercise, MUSCLE PROTEIN-SYNTHESIS, MDX MICE, OXIDATIVE CAPACITY, MYOSTATIN, EXERCISE, DENSITY, METAANALYSIS, DEFICIENCY, PREVENTS, BLOCKING, 3126 Surgery, anesthesiology, intensive care, radiology, 3121 Internal medicine
Publisher: BioMed Central Ltd
Year: 2017
OAI identifier: oai:helda.helsinki.fi:10138/180158
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