In mice with calvarial defects, rPTH increased defect window closure more than sodium cromolyn, which exceeded placebo.
In plain wordsIn mice with skull defects, teriparatide increased defect closure more than sodium cromolyn, which exceeded placebo.
- Peptide
- Teriparatide (PTH 1-34)
- Outcome
- IncreaseDefect window closure versus placebo
- Study
mousen: not reported in source
Critical calvaria defect- Comparator
- Saline placebo
- Outcome group
- Bone and joint · Musculoskeletal
- Studied dose
- 20 μg/kg/2 daysAs given in this study (mouse).
Source sentences
μCT demonstrated that SC significantly increased defect window closure and new bone volume versus placebo (p < 0.05), although these effects were not as great as rPTH.
2 context sentences(design, population, supporting numbers)
To better understand these non-anabolic effects, we interrogated osteogenesis, vasculogenesis, and mast cell accumulation in mice randomized to placebo (saline), rPTH (20 μg/kg/2 days), or the mast cell inhibitor sodium cromolyn (SC)
(24 μg/kg/ 2days), via longitudinal micro-computed tomography (μCT) and multiphoton laser scanning microscopy (MPLSM), in a critical calvaria defect model.