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The Tibial Fracture-Pin Model: A Clinically Relevant Mouse Model of Orthopedic Injury
Published on: July 28, 2022
Pain after osteoporotic fractures using mouse models and patient samples
A Radulescu1, M Hopkinson1, Y Chang1
1Department of Comparative Biomedical Sciences, Royal Veterinary College, 4 Royal College Street, London, NW1 OTU, UK.
Osteoporosis (bone loss) alone does not cause pain in mice, but it can worsen pain after a fracture. Circulating nerve markers did not correlate with pain in osteoporotic patients.
Area of Science:
- Biomedical research
- Pain mechanisms
- Osteoporosis research
Background:
- Osteoporosis is linked to chronic pain, but underlying mechanisms remain unclear.
- Investigating pain behaviors and molecular markers in osteoporosis and fracture models is crucial.
Purpose of the Study:
- To explore pain behaviors and nociceptive marker expression in mouse models of osteoporosis and fracture.
- To quantify nerve markers in serum of osteoporotic patients with or without fractures and pain.
Main Methods:
- Ovariectomy (OVX) or sham surgery in mice, followed by femoral osteotomy or sham osteotomy.
- Assessment of pain behaviors, gene expression (RT-PCR) in bone and dorsal root ganglia (DRGs).
- Quantification of serum nerve markers in osteoporotic patients using ELISAs.
Main Results:
- Ovariectomy alone did not alter pain behaviors or nociceptive gene expression.
- Osteotomy and sham osteotomy affected pain behaviors, but not significantly gene expression.
- OVX prior to osteotomy worsened weight-bearing in mice.
- No correlation found between serum nerve markers and fracture pain in osteoporotic patients.
Conclusions:
- Ovariectomy and bone loss are insufficient to induce pain behaviors in mice but can exacerbate pain post-fracture.
- Clinical analysis revealed no correlation between circulating nerve markers and patient-reported fracture pain.
- Potential sex differences in pain markers warrant further investigation.
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