Tissue selective effects of bazedoxifene on the musculoskeletal system in female mice

Author:

Cabelka Christine A12,Baumann Cory W1,Lindsay Angus13,Norton Andrew4,Blixt Nick C5,Le Gengyun1,Warren Gordon L6,Mansky Kim C4,Novotny Susan A17,Lowe Dawn A1

Affiliation:

1. 1Divisions of Rehabilitation Science and Physical Therapy, Department of Rehabilitation Medicine, Medical School, University of Minnesota, Minneapolis, Minnesota, USA

2. 2Department of Physical Therapy, The College of St. Scholastica, Duluth, Minnesota, USA

3. 3Department of Biochemistry, Molecular Biology and Biophysics, University of Minnesota, Minneapolis, Minnesota, USA

4. 4Department of Developmental and Surgical Sciences, University of Minnesota, School of Dentistry, Minneapolis, Minnesota, USA

5. 5Department of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, Minnesota, USA

6. 6Department of Physical Therapy, Georgia State University, Atlanta, Georgia, USA

7. 7Gillette Children’s Specialty Healthcare, Saint Paul, Minnesota, USA

Abstract

The actions of selective estrogen receptor modulators are tissue dependent. The primary objective of the current study was to determine the tissue selective effects of bazedoxifene (BZA) on the musculoskeletal system of ovariectomized (OVX) female mice, focusing on the strengths of muscle-bone pairs in the lower hindlimb. Treatment with BZA after ovariectomy (OVX+BZA) did not prevent body or fat mass gains (P < 0.05). In vivo plantarflexor muscle isometric torque was not affected by treatment with BZA (P = 0.522). Soleus muscle peak isometric, concentric and eccentric tetanic force production were greater in OVX+BZA mice compared to OVX+E2 mice (P ≤ 0.048) with no effect on maximal isometric specific force (P = 0.228). Tibia from OVX+BZA mice had greater cortical cross-sectional area and moment of inertia than OVX mice treated with placebo (P < 0.001), but there was no impact of BZA treatment on cortical bone mineral density, cortical thickness, tibial bone ultimate load or stiffness (P ≥ 0.086). Overall, these results indicate that BZA may be an estrogen receptor agonist in skeletal muscle, as it has previously been shown in bone, providing minor benefits to the musculoskeletal system.

Publisher

Bioscientifica

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

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