Key result
Spinal epidural stimulation plus training and pharmacology enables rat hindlimb stepping but highlights SCI translational gaps.
This review highlights the translational gap between successful epidural stimulation for locomotion in spinal rats versus humans, emphasizing the role of motor training and pharmacology.
Does not support clinical use in complete SCI; leaves open whether combined epidural stimulation, training, and pharmacology restores locomotion in humans.
Significant advancements in spinal epidural stimulation (ES) strategies to enable volitional motor control in persons with a complete spinal cord injury (SCI) have generated much excitement in the field of neurorehabilitation. Still, an obvious gap lies in the ability of ES to effectively generate a robust locomotor stepping response after a complete SCI in rodents, but not in humans. In order to reveal potential discrepancies between rodent and human studies that account for this void, in this review, we summarize the findings of studies that have utilized ES strategies to enable successful hindlimb stepping in spinal rats. Recent clinical and preclinical evidence indicates that motor training with ES plays a crucial role in tuning spinal neural circuitry to generate meaningful motor output. Concurrently administered pharmacology can also facilitate the circuitry to provide near optimal motor performance in SCI rats. However, as of today, the evidence for pharmacological agents to enhance motor function in persons with complete SCI is insignificant. These and other recent findings discussed in this review provide insight into addressing the translational gap, guide the design of relevant preclinical experiments, and facilitate development of new approaches for motor recovery in patients with complete SCIs.
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Shah et al. (2017) conducted a review in Complete spinal cord injury (SCI). Spinal epidural stimulation (ES) was evaluated. Spinal epidural stimulation combined with motor training and pharmacology enables successful hindlimb stepping in spinal rats, highlighting a translational gap for humans with complete SCI.
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