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Department of Neurology, University of Pennsylvania, Philadelphia, PA.
We studied the effect of systemically administered 4-aminopyridine in a model of CNS demyelination. In five rats with demyelination, slowed conduction velocity through the lesion was partially reversed at dose levels of 5.6 to 7.2 mg/kg. All rats developed convulsion at this dosage, and impaired conduction of high-frequency impulses was unchanged. These findings suggest certain limitations of 4-aminopyridine as a therapeutic agent.
Address correspondence and reprint requests to Dr. Kaji, Department of Neurology, Louisiana State University Medical Center, 1542 Tulane Avenue, New Orleans, LA 70124.
Presented in part at the thirty-ninth annual meeting of the American Academy of Neurology, New York, NY, April 1987.
Received April 21, 1988. Accepted for publication in final form June 29, 1988.
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