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  4. Therapeutic mechanism of basic fibroblast growth factor on spinal cord injury in rats based on the Notch/signal transducer and activator of transcription 3 signaling pathway

Therapeutic mechanism of basic fibroblast growth factor on spinal cord injury in rats based on the Notch/signal transducer and activator of transcription 3 signaling pathway

Chinese Journal of Reparative and Reconstructive Surgery, 2024 · DOI: 10.7507/1002-1892.202312066 · Published: April 1, 2024

Spinal Cord InjuryGenetics

Simple Explanation

This study investigates the potential of bFGF to treat spinal cord injuries in rats by influencing the Notch/STAT3 signaling pathway. The researchers created a spinal cord injury model in rats and then treated them with bFGF to observe its effects on motor function and tissue repair. The experiment involved comparing rats treated with bFGF to a control group (model group) and a sham-operation group. They evaluated the rats' hind limb function using BBB scoring and examined spinal cord tissue samples for signs of neuronal survival, apoptosis, and inflammation. The findings suggest that bFGF treatment can improve motor function, reduce tissue damage, and promote neuronal survival in rats with spinal cord injuries. The proposed mechanism involves the downregulation of the Notch/STAT3 signaling pathway, which is associated with reduced inflammation and astrocyte activation.

Study Duration
28 d
Participants
40 10-week-old male Sprague Dawley (SD) rats
Evidence Level
Not specified

Key Findings

  • 1
    bFGF treatment improved motor function in SCI rats, as evidenced by increased BBB scores compared to the model group.
  • 2
    bFGF reduced spinal cord tissue damage, including decreased necrotic lesions and increased the number of normally structured Nissl bodies.
  • 3
    bFGF suppressed the Notch/STAT3 signaling pathway activity, leading to reduced levels of p-STAT3/STAT3 and BMP-2 proteins in the spinal cord tissue.

Research Summary

This study explored the therapeutic effects of bFGF on spinal cord injury (SCI) in rats, focusing on the Notch/STAT3 signaling pathway. The results indicated that bFGF could improve motor function and repair pathological damage in spinal cord tissue. The research demonstrated that bFGF promotes neuronal survival, inhibits neuronal apoptosis, and reduces excessive activation of astrocytes and inflammation in the spinal cord tissue. These effects are possibly mediated by the downregulation of the Notch/STAT3 signaling pathway. The study concludes that bFGF has the potential to be a therapeutic agent for SCI by modulating the Notch/STAT3 signaling pathway and reducing inflammation and tissue damage in the spinal cord.

Practical Implications

Therapeutic Potential

bFGF shows promise as a potential therapeutic agent for spinal cord injury.

Signaling Pathway Modulation

The Notch/STAT3 signaling pathway is a key target for SCI treatment.

Neuroprotection

bFGF can promote neuronal survival and reduce apoptosis in SCI.

Study Limitations

  • 1
    The study did not explore different dosages of bFGF to optimize treatment.
  • 2
    The study lacked a recovery experiment using Notch/STAT3 signaling pathway activators.
  • 3
    The molecular mechanisms are not fully understood.

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