The purpose of the present study was to prove whether homologous GH has a s
timulating effect on bone healing. Therefore, left tibiae of 30 micropigs w
ere osteomized and distracted over an external fixator at the rate of 2 mm/
day on each of 10 consecutive days. Animals were killed after a healing per
iod of another 10 days. The treatment group received 100 mu g of recombinan
t porcine growth hormone (rpGH) per kilogram of body weight per day. Serial
torsional nondestructive biomechanical tests were performed in vivo using
a newly developed measurement device. After killing, destructive torsional
strength testing of the sites of distraction was performed. To determine th
e endocrine response to the administration of rpGH, serum levels of insulin
-like growth factor-I (IGF-I) were determined. Nondestructive in vivo testi
ng showed that torsional stiffness of the regenerate was significantly high
er in the treatment group than in the control group. Final regenerate torsi
onal failure load was 131% higher and ultimate torsional stiffness was 231%
higher in the treatment group than in the control group. The mean serum le
vel of IGF-I increased to 440% of preoperative basal level in the treatment
group and remained unchanged in the control group. Our data indicate that
systemic administration of recombinant homologous growth hormone greatly ac
celerates ossification of bone regenerate in distraction osteogenesis, (Bon
e 24:81-88; 1999) (C) 1999 by Elsevier Science Inc. All rights reserved.