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  4. Delayed xenon post-conditioning mitigates spinal cord ischemia/reperfusion injury in rabbits by regulating microglial activation and inflammatory factors

Delayed xenon post-conditioning mitigates spinal cord ischemia/reperfusion injury in rabbits by regulating microglial activation and inflammatory factors

Neural Regen Res, 2018 · DOI: 10.4103/1673-5374.228757 · Published: March 1, 2018

Spinal Cord InjuryNeurologyGenetics

Simple Explanation

This study investigates how xenon, a noble gas, can protect the spinal cord from injury after a period of reduced blood flow (ischemia) followed by the restoration of blood flow (reperfusion). The researchers used a rabbit model to examine the effects of giving xenon at different times after the blood flow was restored. They compared giving xenon immediately after reperfusion to giving it two hours later. The study also looked at the impact of these treatments on the activation of microglia, which are immune cells in the spinal cord, and the release of inflammatory factors, which can contribute to spinal cord damage. The findings suggest that delaying the administration of xenon for two hours after reperfusion provides better protection against spinal cord injury in rabbits. This delayed treatment helped to reduce the activation of microglia and the release of harmful inflammatory factors.

Study Duration
Not specified
Participants
24 male New Zealand rabbits
Evidence Level
Level II; Animal study

Key Findings

  • 1
    Delayed xenon post-conditioning significantly improved neurological function in rabbits and attenuated the microglia-mediated inflammatory response.
  • 2
    Immediate xenon post-conditioning amplified the microglia-mediated inflammatory response.
  • 3
    IL-6 and IL-10 levels were significantly increased in the P0 group compared with the P2 and I/R groups.

Research Summary

This study investigated the effects of immediate and delayed xenon post-conditioning on spinal cord ischemia/reperfusion injury (SCI/RI) in rabbits, focusing on microglial activation and inflammatory factors. The key finding was that delayed xenon post-conditioning significantly improved neurological function and reduced the microglia-mediated inflammatory response, while immediate xenon post-conditioning amplified this inflammatory response. The study suggests that the timing of xenon administration is crucial for its neuroprotective effects, with delayed administration showing better outcomes in mitigating SCI/RI by suppressing microglial activation.

Practical Implications

Therapeutic Timing

The timing of xenon administration after spinal cord ischemia/reperfusion injury is critical for achieving neuroprotective effects.

Microglial Modulation

Xenon post-conditioning can modulate microglial activation, influencing the inflammatory response and subsequent spinal cord damage.

Inflammatory Response

Delayed xenon post-conditioning can mitigate the inflammatory response, potentially improving outcomes in spinal cord ischemia/reperfusion injury.

Study Limitations

  • 1
    The study was performed in a rabbit model and needs validation in other animal models.
  • 2
    The analysis only focused on microglia and did not assess astrocytes.
  • 3
    The effects of xenon on inflammatory responses and microglial polarization should be evaluated over a longer period.

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