Long-term effects of methylprednisolone following transection of adult rat spinal cord

Martin Oudega, C. G. Vargas, A. B. Weber, N. Kleitman, Mary B Bunge

Research output: Contribution to journalArticle

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Abstract

Clinically, high-dose treatment with the glucocorticosteroid, methylprednisolone (MP), within 8 h after spinal cord injury, has been shown to improve neurological recovery. The current standard of care is to administer MP as a bolus of 30 mg/kg followed by a 23-h infusion of 5.4 mg/kg/h to spinal cord injured patients. To better understand the role of MP in neuroprotection, we have studied how MP administration affects macrophage accumulation, tissue loss, and axonal dieback at 1, 2, 4 and 8 weeks after a complete transection of the eighth thoracic spinal cord in the adult rat. A 30 mg/kg dose of MP was administered intravenously at 5 min, and 2 and 4 h after injury. The number of ED1 (antibody against microglia/macrophages) -positive cells was quantified in a 500-μm-wide strip of tissue directly adjacent and parallel to the transection. At all time points, MP treatment led to a significant decrease in the number of ED1-positive cells in both rostral and caudal stumps. Over the 2-month post-transection period, the average MP-induced reduction in the number of ED1-positive cells was 82% in the rostral cord stump and 66% in the caudal stump. Using a computerized image analysis system, it was observed that MP treatment resulted in a significant reduction in tissue loss in both cord stumps at 2, 4 and 8 week post-injury. Over the 2-month post-lesion period, the average MP-induced reduction in tissue loss in the caudal cord stump was higher than that in the rostral stump; 48 versus 37%, respectively. Immunostaining for neurofilaments and growth-associated protein-43 (GAP-43) revealed the presence of numerous axons near and in the lesion site. Anterograde neuronal tracing with biotinylated dextran amine showed that, in MP-treated animals, dieback of vestibulospinal fibres, but not of corticospinal fibres, was significantly diminished at all time points studied. In addition, with MP administration, 1 and 2 weeks after injury, an increase in the number of vestibulospinal fibres was found at 1 and 2 mm from the transection, suggesting transient regenerative sprouting of these fibres. The results demonstrate that treatment with MP shortly after spinal cord transection in the adult rat led to a long-term reduction of ED1-positive cells and spinal tissue loss, reduced dieback of vestibulospinal fibres, and a transient sprouting of vestibulospinal fibres near the lesion at 1 and 2 weeks post-lesion. The possible relationships between the inflammatory changes, spinal tissue sparing, and axonal survival and sprouting are complex and need to be further explored.

Original languageEnglish
Pages (from-to)2453-2464
Number of pages12
JournalEuropean Journal of Neuroscience
Volume11
Issue number7
DOIs
StatePublished - Jul 5 1999

Fingerprint

Methylprednisolone
Spinal Cord
Spinal Cord Injuries
Wounds and Injuries
Macrophages
GAP-43 Protein
Intermediate Filaments
Microglia
Standard of Care
Axons
Thorax
Therapeutics

Keywords

  • CNS regeneration
  • Dieback
  • ED1
  • Inflammation
  • Macrophages
  • Secondary damage

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

Long-term effects of methylprednisolone following transection of adult rat spinal cord. / Oudega, Martin; Vargas, C. G.; Weber, A. B.; Kleitman, N.; Bunge, Mary B.

In: European Journal of Neuroscience, Vol. 11, No. 7, 05.07.1999, p. 2453-2464.

Research output: Contribution to journalArticle

Oudega, Martin ; Vargas, C. G. ; Weber, A. B. ; Kleitman, N. ; Bunge, Mary B. / Long-term effects of methylprednisolone following transection of adult rat spinal cord. In: European Journal of Neuroscience. 1999 ; Vol. 11, No. 7. pp. 2453-2464.
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