Osteogenic growth peptide, a
histone H4-related, 14-amino-acid
peptide, is an active mediator of local, as well as systemic, osteogenic activity in response to marrow ablation,
trauma, and blood loss. In this study, the effect of exogenous
osteogenic growth peptide on the healing of
femoral fractures in rats was investigated. A fracture at the midshaft of the femur was created in 50 rats. Half of the rats were injected subcutaneously with 25 ng of
osteogenic growth peptide per rat per day for the first 7 days after fracture. Radiographs were taken each week, and the diameter of the callus was measured. The femurs of four animals from each group were harvested 1, 2, 3, and 4 weeks after fracture. Two femurs from each group were sectioned for histologic examination, and two were sectioned for measurement of density and
mineral content. Marrow was aspirated from the contralateral femurs to establish adhering cell cultures, which were examined for osteogenicity. At 2 weeks, a large increase in mitogenicity and osteogenicity was seen in the marrow-derived cultures from the rats treated with
osteogenic growth peptide; this increase was sustained through 4 weeks. Extraction of
RNA from the contralateral marrow (systemic expression) and callus (local expression) for amplification with reverse transcription-polymerase chain reaction revealed greater systemic expression of
transforming growth factors beta1, beta2, and beta3,
fibroblast growth factor-2,
insulin-like growth factor-1, and
aggrecan throughout the 4 weeks after fracture, whereas types IIA and IIB
collagen,
link protein, and
fibroblast growth factor receptor-3 had a greater local expression. The specimens treated with
osteogenic growth peptide had a stronger expression of
transforming growth factor-beta1, both locally and systemically. The average diameter of the callus was greater for the treated rats at all time intervals, and peak diameters were 7.58 mm at 3 weeks for the treated rats and 6.64 mm at 2 weeks and 6.63 mm at 3 weeks for the controls. Histological study revealed an earlier organization and faster healing of the treated fractures, as evidenced by the larger, earlier appearance of cartilaginous soft callus and the more rapid organization of bridging trabecular bone. No statistical significance was obtained when these comparisons were made between the groups. These results suggest that
osteogenic growth peptide can be used to promote earlier proliferation and differentiation of osteogenic cells in marrow and bone-repair callus, possibly through its effect on the
transforming growth factor-beta family.