Neuroprotective Effect of Epidural Electrical Stimulation against Ischemic Spinal Cord Injury in Rats

Author:

Kakinohana Manabu1,Harada Hideki2,Mishima Yasunori3,Kano Tatsuhiko4,Sugahara Kazuhiro5

Affiliation:

1. Associate Professor.

2. Assistant Professor, Neuroanesthesia Research Labaoratory, Cognitive and Molecular Institute of Brain Diseases, Kurume University, Fukuoka, Japan, and Department of Anesthesiology, School of Medicine, Kurume Unviersity, Kurume, Fukuoka, Japan.

3. Instructor.

4. Professor, Department of Anesthesiology, School of Medicine, Kurume University, Kurume, Fukuoka, Japan.

5. Professor, Department of Anesthesiology, Faculty of Medicine, University of the Ryukyus.

Abstract

Background Electroconvulsion therapy is likely to serve as an effective preconditioning stimulus for inducing tolerance to ischemic brain injury. The current study examines whether electrical stimuli on the spinal cord is also capable of inducing tolerance to ischemic spinal cord injury by transient aortic occlusion. Methods Spinal cord ischemia was induced by occlusion of the descending thoracic aorta in combination with maintaining systemic hypotension (40 mmHg) during the procedure. Animals implanted with epidural electrodes were divided into four groups according to electrical stimulation and sham. Two groups consisted of rapid preconditioning (RE group, n = 8) and sham procedure (RC group, n = 8) 30 min before 9 min of spinal cord ischemia. In the two groups that underwent delayed preconditioning, rats were exposed to 9 min of aortic occlusion 24 h after either pretreatment with epidural electrical stimulation (DE group, n = 8) or sham (DC group, n = 8). In addition, rats were exposed to 6-11 min of spinal cord ischemia at 30 min or 24 h after epidural electrical stimulation or sham stimulation. The group P50 represents the duration of spinal cord ischemia associated with 50% probability of resultant paraplegia. Results Pretreatment with electrical stimulation in the DE group but not the RE group protected the spinal cord against ischemia, and this stimulation prolonged the P50 by approximately 15.0% in the DE group compared with the DC group. Conclusions Although the optimal setting for this electrical preconditioning should be determined in future studies, the results suggest that epidural electrical stimulation will be a useful approach to provide spinal protection against ischemia.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Anesthesiology and Pain Medicine

Reference35 articles.

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