Abstract

Oxidative damage to the diaphragm as a result of cervical spinal cord injury (SCI) promotes muscle atrophy and weakness. Respiratory insufficiency is the leading cause of morbidity and mortality in cervical spinal cord injury (SCI) patients, emphasizing the need for strategies to maintain diaphragm function. Hyperbaric oxygen (HBO) increases the amount of oxygen dissolved into the blood, elevating the delivery of oxygen to skeletal muscle and reactive oxygen species (ROS) generation. It is proposed that enhanced ROS production due to HBO treatment stimulates adaptations to diaphragm oxidative capacity, resulting in overall reductions in oxidative stress and inflammation. Therefore, we tested the hypothesis that exposure to HBO therapy acutely following SCI would reduce oxidative damage to the diaphragm muscle, preserving muscle fiber size and contractility. Our results demonstrated that lateral contusion injury at C3/4 results in a significant reduction in diaphragm muscle-specific force production and fiber cross-sectional area, which was associated with augmented mitochondrial hydrogen peroxide emission and a reduced mitochondrial respiratory control ratio. In contrast, rats that underwent SCI followed by HBO exposure consisting of 1 h of 100% oxygen at 3 atmospheres absolute (ATA) delivered for 10 consecutive days demonstrated an improvement in diaphragm-specific force production, and an attenuation of fiber atrophy, mitochondrial dysfunction and ROS production. These beneficial adaptations in the diaphragm were related to HBO-induced increases in antioxidant capacity and a reduction in atrogene expression. These findings suggest that HBO therapy may be an effective adjunctive therapy to promote respiratory health following cervical SCI.

Highlights

  • Cervical spinal cord injury (SCI) compromises respiratory function as a result of damage to respiratory neural circuitry required for diaphragm muscle contraction [1]

  • No differences in body weight existed between groups prior to the initiation of the experimental protocol non-injured, room air exposure (CON) = 240.1 ± 2.7 g; lateral-cervical spinal cord contusion (SCI) = 230.8 ± 4.3 g; lateral-cervical spinal cord contusion, Hyperbaric oxygen (HBO) therapy (SCI + HBOT) = 232.0 ± 2.9 g)

  • At stimulation frequencies of 60–160 Hz, diaphragm muscle force production from the SCI + HBOT group remained significantly elevated compared to the SCI group, but specific force was depressed compared to the CON group

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Summary

Introduction

Cervical spinal cord injury (SCI) compromises respiratory function as a result of damage to respiratory neural circuitry required for diaphragm muscle contraction [1]. Following cervical SCI, the development of diaphragm dysfunction increases the risk of respiratory complications, morbidity and mortality as a result of atelectasis, pneumonia and ventilator dependence [3]. Preserving diaphragm muscle health by mitigating atrophy and improving contractility should facilitate respiratory rehabilitation and positive respiratory outcomes after cervical SCI. Administration of the antioxidant Trolox immediately following SCI mitigates much of the diaphragm weakness while reducing mitochondrial and oxidative damage [5].

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