Journal of Southern Medical University ›› 2013, Vol. 33 ›› Issue (02): 182-.

Previous Articles     Next Articles

Effects of signaling-selective parathyroid hormone peptide analog on fracture healing in orchiectomized mouse models

  

  • Online:2013-02-20 Published:2013-02-20

Abstract: Objective To assess the effect of intermittent subcutaneous injections of signal-selective parathyroid hormone (PTH)
peptide analog on fracture healing in orchiectomized mouse models. Methods Thirty-six 7-week-old C57/BL male mice were
orchiectomized and injected with hPTH(1-34), the signal-selective PTH peptide analog [Gly1, Arg19]hPTH (1-34), or an identical
volume of vehicle 1 week after induction of femoral fracture. At 14 and 28 days after the operation, the mice were sacrificed for
measurement of bone mineral density (BMD) and bone mineral content (BMC) of the callus using by dual energy X-ray
absorptiometry. The bone healing was evaluated by radiography, biomechanical testing, micro-computed tomography
(Micro-CT) and histological examination. Results At 14 days after the operation, BMD in PTH peptide analog group was
significantly increased (P<0.05). The mouse models treated with the PTH peptide analog showed significantly lower ultimate
bending force and bending rigidity than those with hPTH(1-34) treatment. X-ray and Micro-CT scanning showed that callus
transformation and remodeling was better in PTH peptide analog group than in the vehicle control group but poorer than in
hPTH(1-34) group. Conclusion The signaling-selective PTH peptide analog G1, R19 (1-28) can accelerate fracture healing in
orchiectomized mouse models, in which process cAMP/PKA pathway plays an important role.