Low-intensity (<100 mW/cm(2)) pulsed ultrasound (US) is an established ther
apy for fracture repair. In both animal and human trials, such US has been
shown to facilitate fresh fracture repair and initiate healing in fractures
with repair defects. However, the mechanism by which US achieves these out
comes is not clear. One possible mechanism is the direct stimulation of bon
e formation. To investigate this hypothesis, the current study investigated
the mRNA response of isolated bone-forming cells (UMR-106 cells) to a sing
le 20-min dose of low-intensity pulsed US. Using a novel US-cell coupling m
ethod, US was found to stimulate expression of the immediate-early response
genes c-fos and COX-2 and elevate mRNA levels for the bone matrix proteins
ALP and OC. These findings suggest that low-intensity pulsed US has a dire
ct effect on bone formation. This may contribute to the beneficial effect o
f low-intensity pulsed US on fracture repair. (C) 2001 Academic Press.