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  • Effects of low intensity pulsed acoustic wave retains bone's microstructural and mechanical integrity in a disuse osteopenia mice model

    Paper number

    IAC-13,A1,2,5,x20268

    Author

    Prof. Yi-Xian Qin, State University of New York, United States

    Coauthor

    Dr. Sardar Zia Uddin, United States

    Year

    2013

    Abstract
    INTRODUCTION
    Long-term bedrest, brain/spinal cord injury, and space travel induce bone loss due to lack of mechanical stress, which lead to the risk of osteoporosis and fracture. Different anabolic and anti-resorptive agents have been used to mitigate bone loss under such conditions. However, the results for these treatments have been mixed, in part due to the localized nature of disuse induced bone loss which is concentrated on load bearing bones. It is hypothesized that modulated low intensity pulsed ultrasound (mLIPUS) generated acoustic wave can provide anabolic and targeted stimulus to reduce bone loss in disuse osteopenia.  
    METHODS
    Four-month old C57BL/6 mice were randomized to five groups, age match (AM), non-suspended sham (NS), non-suspended –LIPUS (NU), suspended sham (SS), and suspended-LIPUS (SU). LIPUS for 20 min/day for 5 days/week. After four weeks of suspension, µCT analyses were conducted for trabecular structural and density measurements on the parameters of bone volume fraction (BV/TV), bone mineral density (BMD), trabecular thickness (Tb.Th), and bone surface/bone volume (BS/BV). Histomorphometric analyses and mechanical testing were applied for the femur.  
    RESULTS
    µCT showed significant decreases in BV/TV (36\%, p<0.005), BMD (3\%, p<0.05), Tb.Th (12.5%, p<0.005), and increase in BS/BV (16\%,p<0.005), relative to age match (AM). Ultrasound treatment significantly increased BMD (3\%, p<0.05), Tb.Th (6\%, p<0.05), and decreased BS/BV (10\%, p<0.005), relative to suspension alone (SS) mice (Fig.1). Histomorphometric analyses showed a breakdown of bone microstructure under disuse conditions consist with µCT results. In comparison to SS mice, mLIPUS treated showed increased bone formation rates at metaphyseal endosteal and trabecular surfaces (0.104±0.07 vs 0.031±0.30 µm3/ (µm2)/d) relative to SS (Fig.2). 4-point bending test of SS femur showed reduced elastic modulus (53\%, p<0.05), yield (33\%, p<0.05), and ultimate strength (45\%,P<0.05) at the femoral diaphysis relative to AM. mLIPUS stimulation mitigated the adverse effects of disuse on bone elastic modulus (42\%, p<0.05), yield strength (29\%, p<0.05), and ultimate strength (39\%, p<0.05) relative to SS femurs (Fig.3).
    DISCUSSION
    This study explored the potential of mLIPUS as a non-invasive, non- pharmacological targeted therapy for disuse osteoporosis, suggesting that mLIPUS has very strong potential as a non-invasive and targeted anabolic agent for disuse osteoporosis.
    Abstract document

    IAC-13,A1,2,5,x20268.brief.pdf

    Manuscript document

    (absent)