Skip to main content
. 2008 Jun 30;23(11):1722–1730. doi: 10.1359/JBMR.080603

Table 2.

Biomechanical Testing

Parameter Experiment A
Experiment B
PO PO TD TD PO TD TD TD
Dose (mg/kg/d) 0 10 25 1 2.5 0 5 0.1 1 5
N 5 6 6 5 7 9 8 8 8 9
125.5 ± 8.2 135.0 ± 11 138.0 ± 1.1 178.1 ± 12* 149 ± 7.6* 135.4 ± 17.2 161.5 ± 13.7 192.6 ± 17* 175 ± 15.8* 154.2 ± 9.8
Maximum force (N) ↑ 7.6% ↑ 10% ↑ 42% ↑ 18.5% ↑ 19% ↑ 42% ↑ 29% ↑ 14%
321 ± 20.2 559 ± 68.7* 596.2 ± 102* 566 ± 89* 594 ± 26* 252 ± 55 275.4 ± 38 477 ± 58* 382 ± 49* 419 ± 60*
Stiffness (N/mm) ↑ 74% ↑ 85.7% ↑ 76% ↑ 85% ↑ 9% ↑ 90% ↑ 52% ↑ 67%
35.4 ± 15 19.2 ± 1.6 26.6 ± 5.8 57.7 ± 5 27.1 ± 2.5 70.8 ± 16 62.6 ± 13.7 54 ± 8.9 54 ± 13.2 61 ± 8.7
Work to fracture (N-mm) ↑ 63%

Biomechanical testing evaluated at 6 wk by three-point bending for experiments A and B in groups treated with PO and TD lovastatin. Number of femora tested for each treatment groups is indicated in the table. Results are expressed as mean ± SE. Numbers after arrows represent the percentage increase compared with vehicle-treated controls.

* p < 0.02, compared with vehicle control.