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  4. Spinal cord injury modulates the lung inflammatory response in mechanically ventilated rats: a comparative animal study

Spinal cord injury modulates the lung inflammatory response in mechanically ventilated rats: a comparative animal study

Physiol Rep, 2016 · DOI: 10.14814/phy2.13009 · Published: December 1, 2016

Spinal Cord InjuryCritical CarePulmonology

Simple Explanation

Mechanical ventilation (MV) is a common procedure for spinal injury patients. MV can induce lung inflammation. This study examines how spinal cord injury (SCI) interacts with MV to affect lung inflammation. The study found that SCI can reduce some of the lung inflammation caused by MV. Specifically, SCI decreased the expression of IL-1b and reduced oxidative stress responses in the lungs of mechanically ventilated rats. These findings suggest that the interplay between MV and SCI is complex and may have implications for how ventilated SCI patients are treated. Treating ventilated SCI patients may amplify pulmonary biotrauma.

Study Duration
24 h
Participants
33 adult female Sprague Dawley rats
Evidence Level
Animal study

Key Findings

  • 1
    Mechanical ventilation increased levels of TNF-α, IL-1β, and IL-6, while decreasing IL-10 in the bronchoalveolar lavage (BAL) fluid of rats without spinal cord injury.
  • 2
    Cervical spinal cord injury reduced MV-induced pulmonary oxidative stress responses by decreasing isoprostane levels and increasing heme oxygenase-1 levels.
  • 3
    Thoracic spinal cord injury in non-ventilated animals increased M-CSF expression and promoted antioxidant pulmonary responses.

Research Summary

This study investigated the interaction between mechanical ventilation (MV) and spinal cord injury (SCI) on pulmonary inflammation in rats. The researchers measured inflammatory cytokine profiles and oxidative stress mediators in bronchoalveolar lavage (BAL). The results showed that MV increased pro-inflammatory cytokines in BAL, while SCI modulated these responses. Cervical SCI reduced IL-1β levels and oxidative stress, while thoracic SCI increased M-CSF expression and antioxidant responses. The study concludes that SCI modulates MV-induced pulmonary inflammation, with potential clinical implications for treating ventilated SCI patients. Effective treatment of ventilated SCI patients may amplify pulmonary biotrauma.

Practical Implications

Optimizing Ventilation Strategies

Ventilation strategies may need to be adjusted for SCI patients to minimize lung injury.

Targeted Therapies

Targeting specific inflammatory pathways (e.g., IL-1β) could be beneficial in ventilated SCI patients.

Antioxidant Support

Providing antioxidant support may help mitigate oxidative stress in ventilated SCI patients.

Study Limitations

  • 1
    Absence of circulating mediator measurements
  • 2
    Lack of a non-ventilated cervical SCI control group
  • 3
    Short duration of mechanical ventilation (24 h)

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