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  4. Substance P and calcitonin gene-related peptide expression in dorsal root ganglia in sciatic nerve injury rats

Substance P and calcitonin gene-related peptide expression in dorsal root ganglia in sciatic nerve injury rats

Neural Regen Res, 2013 · DOI: 10.3969/j.issn.1673-5374.2013.33.006 · Published: November 1, 2013

Regenerative MedicineNeurology

Simple Explanation

This study investigates the role of substance P and calcitonin gene-related peptide in the repair of sciatic nerve injury in rats. A sciatic nerve defect model was created in rats, and the expression of these neuropeptides in the dorsal root ganglia was examined at different time points. The findings suggest that these neuropeptides play a significant role in the early stages of nerve repair. The researchers found that the expression of substance P and calcitonin gene-related peptide increased significantly in the dorsal root ganglion of rats with sciatic nerve injury. This increase peaked at 7 days, declined at 14 days, and returned to normal levels by 28 days post-injury, suggesting their involvement in early nerve regeneration processes. These neuropeptides are known to transmit pain signals and may also contribute to nerve repair following injury. The study's findings suggest that they could potentially serve as indicators for evaluating early peripheral nerve injury.

Study Duration
Not specified
Participants
40 female Sprague Dawley rats
Evidence Level
Animal study

Key Findings

  • 1
    Substance P and calcitonin gene-related peptide expression in dorsal root ganglia were altered over time in rats with sciatic nerve injury.
  • 2
    The expression of substance P and calcitonin gene-related peptide mainly increased in the early stages after sciatic nerve injury.
  • 3
    Substance P and calcitonin gene-related peptide are involved in transmitting pain signals and play a role in repair following sciatic nerve injury.

Research Summary

This study investigates the expression of substance P and calcitonin gene-related peptide in dorsal root ganglia of rats with sciatic nerve injury. A sciatic nerve defect model was created, and the expression of these neuropeptides was examined at 7, 14, and 28 days post-injury using immunohistochemical staining. The results showed that substance P and calcitonin gene-related peptide expression increased significantly in the dorsal root ganglion of rats with sciatic nerve injury, peaking at 7 days, declining at 14 days, and returning to normal levels by 28 days post-injury. The findings suggest that these neuropeptides mainly increase in the early stages after sciatic nerve injury and may serve as an index for evaluating early peripheral nerve injury.

Practical Implications

Early Diagnostic Marker

Substance P and calcitonin gene-related peptide levels can potentially be used as early indicators of peripheral nerve injury.

Therapeutic Target

Modulating substance P and calcitonin gene-related peptide expression may enhance nerve regeneration after injury.

Pain Management

Understanding the role of these neuropeptides in pain transmission can lead to improved pain management strategies for nerve injuries.

Study Limitations

  • 1
    Animal model may not fully replicate human nerve injury.
  • 2
    Study only assessed expression at specific time points (7, 14, and 28 days).
  • 3
    The mechanism surrounding peripheral nerve injury remains uncertain

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