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  4. Suppression of Superficial Microglial Activation by Spinal Cord Stimulation Attenuates Neuropathic Pain Following Sciatic Nerve Injury in Rats

Suppression of Superficial Microglial Activation by Spinal Cord Stimulation Attenuates Neuropathic Pain Following Sciatic Nerve Injury in Rats

International Journal of Molecular Sciences, 2020 · DOI: 10.3390/ijms21072390 · Published: March 30, 2020

NeurologyPain ManagementGenetics

Simple Explanation

This study investigates how spinal cord stimulation (SCS) reduces neuropathic pain after nerve injury. The researchers focused on the role of microglial activation in the spinal cord, which is known to contribute to pain hypersensitivity. SCS was applied to rats with sciatic nerve injury, and the effects on pain sensitivity, microglial activity, and brain responses were measured. Minocycline, a drug that inhibits microglial activation, was also tested for its effects. The findings suggest that SCS reduces neuropathic pain by suppressing microglial activation in the spinal cord, which in turn reduces neuronal hyperexcitability and alters brain responses to pain stimuli. This indicates SCS could be a useful therapy for neuropathic pain.

Study Duration
Not specified
Participants
81 male Sprague-Dawley rats
Evidence Level
Not specified

Key Findings

  • 1
    SCS and minocycline both reduced plantar mechanical hypersensitivity in rats after spared nerve injury (SNI), indicating a reduction in pain sensitivity.
  • 2
    SCS suppressed the increase in density of activated microglia in the L4 dorsal horn following SNI. Minocycline also showed a trend toward suppressing microglial activation.
  • 3
    SCS reduced the excitability of wide dynamic range (WDR) neurons in the L4-S1 dorsal horn, suggesting a decrease in spinal neuronal hyperexcitability.

Research Summary

This study evaluated the analgesic effects of spinal cord stimulation (SCS) on neuropathic pain following spared nerve injury (SNI) in rats, focusing on the role of microglial activation and neuronal excitability in the spinal cord. The findings suggest that SCS suppresses plantar SNI-induced neuropathic pain by inhibiting microglial activation in the L4 dorsal horn, which is involved in spinal neuronal hyperexcitability. The study also found that electrical stimulation of the hind paw-activated areas in the somatosensory cortex was decreased by SCS, indicating that SCS modulates pain processing at the central nervous system level.

Practical Implications

Alternative Therapy

SCS is likely to be a potential alternative medicine therapy to alleviate neuropathic pain following nerve injury.

Microglial Targeting

The study highlights the importance of microglial activation in neuropathic pain and suggests that targeting microglia could be a therapeutic strategy.

CNS Modulation

SCS modulates pain processing at both the spinal and supraspinal levels, indicating its potential to alter central sensitization.

Study Limitations

  • 1
    The study was conducted in rats and may not directly translate to humans.
  • 2
    The study focused on an early development phase of chronic pain (day 3 post-SNI), which may differ from chronic neuropathic pain.
  • 3
    Further studies are needed to elucidate the precise mechanisms of SCS-induced analgesia in humans.

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