H. Jones et al., Acoustic energy affects human gingival fibroblast proliferation but leavesprotein production unchanged, J CLIN PER, 27(11), 2000, pp. 832-838
Background, aims: Sonic toothbrushes are well-established in oral home care
for plaque removal; however, the effects of low frequency acoustic (sonic)
energy released from sonic toothbrushes to the cells of the periodontium h
ave not been investigated, The purpose of this study was to evaluate the ef
fects of sonic energy on human gingival fibroblast proliferation and protei
n production in cell culture.
Methods: Direct and indirect transfer calibration studies found the fundame
ntal frequency of the Sonicare(R) sonic toothbrush to be 261 hertz (Hz) wit
h amplitudes ranging from 70 to 104 decibels (dB) in the human periodontium
. Using an in vitro delivery system, which coupled a signal-wave generator
with a bone transducer to mimic the energy delivered by the Sonicare(R) too
thbrush, the effects of signal, amplitude and duration were evaluated longi
tudinally using a gingival fibroblast cell culture model. 8 strains of fibr
oblasts isolated from healthy human gingiva were seeded at 30,000 cells/35
mm culture dish in minimum essential medium supplemented with 10% fetal bov
ine serum. To ascertain the relationship of the amplitude and the duration
of sonic stimulation to cellular proliferation, gingival fibroblasts were s
ubjected 2x daily to 261 Hz sound at various amplitudes (67-97 dB) for 0, 1
5, 30, 60, and 120 s on days 1, 3, 5, 7, and 10.
Results: It was found that either 30 or 120 s of sound exposure for 10 days
of treatment had significant effects on cell proliferation in comparison t
o control cultures. Specifically, at day 10, 87 dB at 261 Hz for 30 s 2x da
iry resulted in a 25.5% increase in cell number (p<0.001), whereas 87 dB at
261 Hz for 120 s twice daily caused a 30.9% decrease in cell number (p<0.0
01) when compared to control cultures. When cells are stimulated under opti
mum acoustic conditions for 10 days, there was no difference between the tr
eatment and control groups for collagen (p=0.897) or noncollagen (p=0.697)
protein production.
Conclusions: Sonic energy has been shown to both increase and decrease cell
ular proliferation depending on exposure time, however, during optimum soun
d-induced conditions for cellular proliferation, sonic energy had no effect
on fibroblast protein production. These data suggest that sonic energy can
affect the behavior of cells in culture. Further research into the mechani
sms of these changes will provide important information for manipulating ce
llular behavior.