Protective effect of the NMDA antagonist MK-801 on photochemically induced spinal lesions in the rat

J. X. Hao, B. D. Watson, X. J. Xu, Z. Wiesenfeld-Hallin, Å Seiger, E. Sundström

Research output: Contribution to journalArticlepeer-review

42 Scopus citations

Abstract

Photochemically induced ischemic lesions in the rat spinal cord were studied using neurological tests and morphological evaluation in order to investigate ischemia-mediated pathophysiological mechanisms in traumatic spinal cord injury. One week after ischemic lesioning, animals were severely impaired with 85% decrease of performance in neurological tests. During the next 2 weeks considerable recovery occurred. Pretreatment with the noncompetitive N-methyl-d-aspartate antagonist MK-801 at a dose of 0.5-1.0 mg/kg significantly improved the recovery of function after spinal ischemia while lower doses exerted no protection. Morphologically, no dose-response effect on the extent of tissue necrosis was found, but a significant difference between groups with severe neurological deficit versus mildly affected groups was observed. Immunohistochemical staining for glial fibrillary acidic protein in the area close to the lesion revealed extensive gliosis, while neurofilament immunohistochemistry showed an irregular pattern of fiber loss with large variability between animals. The degree of gliosis or loss of neurofilament immunoreactivity in nonnecrotic tissue was not affected by MK-801. These results suggest that excessive stimulation of N-methyl-d-aspartate receptors participates in the development of spinal cord ischemia and possibly also participates after traumatic spinal cord injury.

Original languageEnglish (US)
Pages (from-to)143-152
Number of pages10
JournalExperimental Neurology
Volume118
Issue number2
DOIs
StatePublished - Nov 1992

ASJC Scopus subject areas

  • Neurology
  • Developmental Neuroscience

Fingerprint Dive into the research topics of 'Protective effect of the NMDA antagonist MK-801 on photochemically induced spinal lesions in the rat'. Together they form a unique fingerprint.

Cite this