Fig. 6: β3AR agonist and CXCR4 antagonist enhances in vivo bone formation.

a–d Rats underwent bilateral posterolateral lumbar fusion surgery followed by rhG-CSF, BRL37344 or vehicle once daily for 4 days. Two hours after the last injection, rats were administered AMD3100 or vehicle. a Representative in vivo NIR fluorescence images of the L4/L5 fusion site at 3 weeks post op. b Representative 3D bone volumes at the L4/L5 fusion site, derived from in vivo µCT scans, at 12 weeks post op. Numerical results of c NIR fluorescence intensity, and d µCT-derived bone volume data. Data represented as individual data points with mean and 95% CI overlaid. n = 8 rats per group; c control vs β3 + AMD3100 aP < 0.01, AMD3100 vs β3 + AMD3100 bP < 0.001; d 6 weeks control vs β3 + AMD3100 aP < 0.05, 12 weeks control/AMD vs β3 + AMD a,bP ≤ 0.001. Twelve weeks control vs rhG-CSF + AMD3100 aP < 0.05 (multiple comparison with Sidak post hoc correction).