Literature DB >> 10391369

Changes in neuronal receptive field characteristics in caudal brain stem following chronic spinal cord injury.

C H Hubscher1, R D Johnson.   

Abstract

Chronic spinal cord injury pain is poorly understood and, thus, not effectively relieved by traditional treatments. In the present study, a variety of partial, severe and sham chronic spinal lesions were made in 31 male rats at spinal level T8. During routine care/handling and brief behavioral testing of the animals throughout the 30-day recovery period, the majority of those with severe contusion injuries (verified histologically) showed signs of mechanical hypersensitivity on the dorsolateral trunk just rostral to the level of injury (i.e., upper thoracic territory). Terminal electrophysiological experiments were performed on all rats (urethane anesthesia). Single unit recordings were made at two supraspinal locations within the caudal brainstem, the nucleus reticularis gigantocellularis and nucleus reticularis gigantocellularis pars alpha. Neurons in these areas normally receive bilateral nociceptive somatovisceral inputs from many parts of the body. Seventy-three percent of the animals with severe contusion injuries developed novel low-threshold neuronal responses to stimulation of the dorsolateral trunk (upper thoracic territory). This amount was significantly greater than for animals with more moderate spinal lesions (dorsal or lateral hemisection; 29% and 25%, respectively) or sham controls (0%). These data suggest (1) that the spinal contusion is a reliable model for studies of the neural mechanisms that underly central spinal cord injury-related pain and (2) that the caudal brainstem is one supraspinal location where neurons undergo significant changes in responsiveness following severe chronic spinal cord injury. The observed plasticity is likely part of the central reorganization producing the multitude of sensory disturbances that surface following spinal cord injury.

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Mesh:

Year:  1999        PMID: 10391369     DOI: 10.1089/neu.1999.16.533

Source DB:  PubMed          Journal:  J Neurotrauma        ISSN: 0897-7151            Impact factor:   5.269


  11 in total

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2.  Segmental neuropathic pain does not develop in male rats with complete spinal transections.

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Review 3.  Cellular transplantation strategies for spinal cord injury and translational neurobiology.

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Review 4.  Neuronal nociceptive responses in thalamocortical pathways.

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Journal:  Neurosci Bull       Date:  2009-10       Impact factor: 5.203

5.  Sex and hormonal variations in the development of at-level allodynia in a rat chronic spinal cord injury model.

Authors:  Charles H Hubscher; Jason D Fell; Daya S Gupta
Journal:  Neurosci Lett       Date:  2010-04-29       Impact factor: 3.046

6.  Differences in forebrain activation in two strains of rat at rest and after spinal cord injury.

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7.  Select spinal lesions reveal multiple ascending pathways in the rat conveying input from the male genitalia.

Authors:  C H Hubscher; W R Reed; E G Kaddumi; J E Armstrong; R D Johnson
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8.  Novel multi-system functional gains via task specific training in spinal cord injured male rats.

Authors:  Patricia J Ward; April N Herrity; Rebecca R Smith; Andrea Willhite; Benjamin J Harrison; Jeffrey C Petruska; Susan J Harkema; Charles H Hubscher
Journal:  J Neurotrauma       Date:  2014-03-25       Impact factor: 5.269

9.  Effects of 17beta-estradiol on responses of viscerosomatic convergent thalamic neurons in the ovariectomized female rat.

Authors:  William R Reed; Harpreet K Chadha; Charles H Hubscher
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10.  Modelling at-level allodynia after mid-thoracic contusion in the rat.

Authors:  Gary H Blumenthal; Bharadwaj Nandakumar; Ashley K Schnider; Megan R Detloff; Jerome Ricard; John R Bethea; Karen A Moxon
Journal:  Eur J Pain       Date:  2021-01-25       Impact factor: 3.931

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