Combined effect of whole-body vibration and parathyroid hormone on bone structure and material properties of ovariectomized mice

Physiology 2016 (Dublin, Ireland) (2016) Proc Physiol Soc 37, PCB207

Poster Communications: Combined effect of whole-body vibration and parathyroid hormone on bone structure and material properties of ovariectomized mice

S. Itamochi1, T. Matsumoto2

1. Graduate School of Engineering Science, Osaka University, Toyonaka, Japan. 2. Graduate School of Science & Technology, Tokushima University, Tokushima, Japan.

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Estrogen deficiency in postmenopausal osteoporosis alters estrogen receptor expressions, thereby elevating bone mechano-responsiveness. Parathyroid hormone (PTH), the first-approved bone anabolic drug, also sensitizes bone cells to mechanical stimuli and lowers the bone-modelling threshold of mechanical strain. Thus, the concurrent use of PTH with mechanical stimuli may be effective in preventing postmenopausal bone loss. We evaluated the combined bone-anabolic effect of PTH and low-intensity whole body vibration (WBV), which could be easily available for treating elderly osteoporotic patients. Female C57BL/6J mice were bilaterally ovariectomized (n=66) at 9 weeks of age and divided into six groups (n=11 each): the control group (C) and the groups treated with PTH (P), sine-wave WBV (s-W) at an acceleration of 0.3 g and 45 Hz for 20 min/day, noise-like WBV (n-W) at a root mean squared acceleration of 0.3g and frequency components of 45 to 100 Hz, s-W combined with PTH (s-W/P), and n-W combined with PTH (n-W/P). Two weeks later, the P, s-W/P, and n-W/P groups were subcutaneously given human PTH (1-34) at a dose of 30 µg/kg/day; the s-W, s-W/P, n-W, and n-W/P groups were exposed to sine-wave or noise-like WBV for 20 min/day. In the combined treatment, PTH was administered 30 min before each WBV session. After 18-day treatment, all mice were euthanized by pentobarbital overdose (i.p.) and the left tibiae were harvested. The proximal metaphyseal region was μCT-scanned, and a volume extending a distance of 1.5 mm distal to the growth plate was reconstructed for structure analysis (9-mm voxel resolution). In addition, its cortical bone cross-section was analyzed by Fourier transform infrared microspectroscopy and nanoindentation testing. Single application of PTH or sine-wave WBV had no effect on bone structure and material properties of cortical bone. In contrast, noise-like WBV and the combination of PTH with either noise-like or sine-wave WBV increased the volume fraction of trabecular bone (Fig. 1, left). Furthermore, the concurrent use increased the trabecular bone connectivity and the hardness of cortical bone (Fig. 1, right); the latter would be attributed to the elevation of mineral maturity. When combined with PTH, noise-like WBV also increased cortical bone and trabecular bone thickness. These results suggest the therapeutic potential of combining WBV with PTH for treating postmenopausal osteoporosis. Noise-like vibration may be more bone-anabolic than stationary vibration.



Where applicable, experiments conform with Society ethical requirements.

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