Targeted Iron Chelation Will Improve Recovery after Spinal Cord Injury

Abstract

Following spinal cord injury there is a protracted accumulation of iron at the site of the injury. Iron plays a role in multiple damaging pathways following injury but is also essential for maximal oligodendrogenesis. The current experiments investigate the therapeutic potential of iron chelation following traumatic spinal cord injury. Our initial research indicates that if iron chelation with the Federal Drug Administration (FDA) approved drug Exjade is begun approximately 1.5 hours after a spinal cord injury there is limited improvement in locomotor function and increased spared of grey matter. Since iron accumulation occurs in a protracted manner, we also investigated the potential of delayed the start of Exjade treatment by 1 week. This paradigm, however, did not result in any of the improvements observed in the early onset treatment. Increasing the dose of Exjade to 320mg/kg/day resulted in increased mortality and therefore was discontinued. In attempts to improve the effects of iron chelation, we have conducted experiments using a different FDA approved chelator, deferiprone. Following either contusive or hemisection spinal cord injury, deferiprone improves functional and histological outcome.

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 2014
Accession Number
AD1001602

Entities

People

  • Dana M. Mctigue

Organizations

  • Ohio State University

Tags

DTIC Thesaurus Topics

  • Biomedical Research
  • Blood
  • Blood-Brain Barrier
  • Cell Physiological Processes
  • Cells
  • Chelation
  • Diseases And Disorders
  • Health Services
  • Hematologic Diseases
  • Hydroxyl Radical
  • Neurology
  • Neurosciences
  • Parkinson'S Disease
  • Spinal Injuries
  • Statistical Analysis
  • Stem Cells
  • Wounds And Injuries

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