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We tested the hypothesis that increased muscle mass augments increases in bone strength normally observed with exercise. Myostatin-deficient mice, which show increased muscle mass, were exercised along with wildtype mice. Results indicate that increases in bone strength with exercise are greater in myostatin-deficient mice than in wildtype mice, suggesting that the combination of increased muscle mass and physical activity has a greater effect on bone strength than either increased muscle mass or intense exercise alone.Introduction: Muscle (lean) mass is known to be a significant predictor of peak BMD in young people, and exercise is also found to increase bone mass in growing humans and laboratory animals. We sought to determine if increased muscle mass resulting from myostatin deficiency would enhance gains in bone strength that usually accompany exercise. Materials and Methods: Male mice lacking myostatin (GDF-8) were used as an animal model showing increased muscle mass. Wildtype and myostatin-deficient mice (n ‫ס‬ 10-12 per genotype) were exercised on a treadmill for 30 minutes/day, 5 days/week, for 4 weeks starting at 12 weeks of age. Caged wildtype and myostatin-deficient mice (n ‫ס‬ 10-12 per genotype) were included as sedentary controls. Structural and biomechanical parameters were measured from the radius. Results: Ultimate force (F u ), displacement (D u ), toughness (energy-to-fracture; U), and ultimate strain ( u ) increased significantly with exercise in myostatin-deficient mice but not in normal mice. When F u is normalized by body mass, exercised myostatin-deficient mice show an increase in relative bone strength of 30% compared with caged controls, whereas exercised wildtype mice do not show a significant increase in ultimate force relative to caged controls. Relative to body weight, the radii of exercised myostatin-deficient mice are >25% stronger than those of exercised normal mice. Conclusions: Increased muscle mass resulting from inhibition of myostatin function improves the positive effects of exercise on bone strength.

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The thermal stability of anatase TiO2 nanoparticles, produced by flame synthesis, is investigated in the current study. Phase-pure anatase particles of ∼4 nm in size can be reproducibly synthesized by using a tubular burner and rotating sampler. Transmission electron microscopy (TEM), glancing incidence X-ray diffraction (XRD), and near-edge X-ray absorption fine structure (NEXAFS) were utilized to characterize the particles before and after annealing to various temperatures. TEM investigations reveal a primary particle size of ∼4 nm with standard deviations around 1 nm. XRD and selected area electron diffraction (SAED) indicate that TiO2 nanoparticles are phase-pure anatase. Our results indicate that the particles remain kinetically trapped upon annealing up to 773 K in air for 2 h. At 973 K, increases in average size, rutile content, and particle shape are observed, consistent with recent reports in the literature. NEXAFS measurements indicate that the O K-edge features of the nanoparticles show similarities to those of surfaces of bulk TiO2.

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