The consequences of spinal cord injury (SCI) are often viewed as the result of white matter damage. However, injuries occurring at any spinal level, especially in cervical and lumbar enlargement regions, also entail segmental neuronal loss. Yet, the contributions of gray matter injury and plasticity to functional outcomes are poorly understood. The present study addressed this issue by investigating changes in respiratory function following bilateral C-3/C-4 contusion injuries at the level of the phrenic motoneuron (PhMN) pool which in the adult rat extends from C-3 CO C-5/6 and provides innervation to the diaphragm. Despite extensive white and gray matter pathology associated with two magnitudes of injury severity, ventilation was relatively unaffected during both quiet breathing and respiratory challenge (hypercapnia). On the other hand, bilateral diaphragm EMG recordings revealed that the ability to increase diaphragm activity during respiratory challenge was substantially, and chronically, impaired. This deficit has not been seen following predominantly white matter lesions at higher cervical levels. Thus, the impact of gray matter damage relative to PhMNs and/or interneurons becomes evident during conditions associated with increased respiratory drive. Unaltered ventilatory behavior, despite significant deficits in diaphragm function, suggests compensatory neuroplasticity involving recruitment of other spinal respiratory networks which may entail remodeling of connections. Transynaptic tracing, using pseudorabies virus (PRV), revealed changes in PhMN-related interneuronal labeling rostral to the site of injury, thus offering insight into the potential anatomical reorganization and spinal plasticity following cervical contusion. (C) 2011 Elsevier Inc. All rights reserved.
Respiratory function following bilateral mid-cervical contusion injury in the adult rat
Creators
Michael A. Lane - McKnight Brain Institute
Kun-Ze Lee - University of Florida College of Public Health and Health Professions
Krystal Salazar - McKnight Brain Institute
Barbara E. O'Steen - McKnight Brain Institute
David C. Bloom - University of Florida
David D. Fuller - University of Florida College of Public Health and Health Professions
Paul J. Reier - McKnight Brain Institute
Publication Details
Experimental neurology, v 235(1), pp 197-210
Publisher
Elsevier
Number of pages
14
Grant note
Paralyzed Veterans of America
UL1TR000064 / NATIONAL CENTER FOR ADVANCING TRANSLATIONAL SCIENCES; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Center for Advancing Translational Sciences (NCATS)
R01NS054025 / NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Institute of Neurological Disorders & Stroke (NINDS)
Anne and Oscar Lackner Chair
R21HL104294 / NATIONAL HEART, LUNG, AND BLOOD INSTITUTE; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Heart Lung & Blood Institute (NHLBI)
RO1 NS054025; R21 HL104294 / National Institute of Health; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA
Resource Type
Journal article
Language
English
Academic Unit
Neurobiology and Anatomy
Web of Science ID
WOS:000303430400021
Scopus ID
2-s2.0-84859903722
Other Identifier
991019298759804721
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