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Intracerebral infusion of a second-generation ciliary neurotrophic factor reduces neuronal loss in rat striatum following experimental intracerebral hemorrhage.

Abstract
Neuronal and glial cell death in the striatum of a rat model of collagenase-induced intracerebral hemorrhage begins at 1 day and continues for at least 3 weeks. We hypothesized that administration of a neurotrophic agent would reduce neuronal loss in this experimental model. Because it has been shown to protect striatal neurons against excitotoxic injury, a second-generation ciliary neurotrophic factor (CNTF) (AXOKINE) was administered by continuous intracerebral infusion (2 microg/day) beginning 28 h after hemorrhage and continuing for 2 weeks. Magnetic resonance imaging showed that the hematoma size was comparable in control and treated rats prior to treatment. Counts of medium-sized striatal neurons within 320 microm of the hematoma 8 weeks after the hemorrhage revealed a slight but statistically significant benefit with a 42.5% loss in treated rats compared to 51.7% loss in controls. The results suggest that AXOKINE might be protective of striatal neurons in the vicinity of a hemorrhagic lesion.
AuthorsM R Del Bigio, H J Yan, M Xue
JournalJournal of the neurological sciences (J Neurol Sci) Vol. 192 Issue 1-2 Pg. 53-9 (Nov 15 2001) ISSN: 0022-510X [Print] Netherlands
PMID11701153 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Ciliary Neurotrophic Factor
  • Nerve Tissue Proteins
  • Neuroprotective Agents
  • Recombinant Proteins
  • axokine
Topics
  • Animals
  • Basal Ganglia Hemorrhage (drug therapy, pathology, physiopathology)
  • Cell Death (drug effects, physiology)
  • Cell Survival (drug effects, physiology)
  • Cerebral Hemorrhage (drug therapy, pathology, physiopathology)
  • Ciliary Neurotrophic Factor (pharmacology)
  • Corpus Striatum (drug effects, pathology, physiopathology)
  • Disease Models, Animal
  • In Situ Nick-End Labeling
  • Male
  • Necrosis
  • Nerve Degeneration (drug therapy, pathology, physiopathology)
  • Nerve Tissue Proteins (pharmacology)
  • Neuroglia (drug effects, metabolism, pathology)
  • Neurons (drug effects, metabolism, pathology)
  • Neuroprotective Agents (pharmacology)
  • Rats
  • Rats, Sprague-Dawley
  • Recombinant Proteins (pharmacology)
  • Treatment Outcome

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