Demyelination of axons within the spinal cord represents a significant
component of the pathology of contusive and compressive spinal cord i
njury (SCI) and the associated conduction deficits most probably contr
ibute to the paralysis and sensory loss experienced by SCI patients. 4
-Aminopyridine (4-AP) is a potassium (K+) channel blocking agent that
has been shown capable of restoring conduction across demyelinated int
ernodes in neurons of the spinal cord. Recent clinical trials of 4-AP
provide evidence that limited and transient neurological gain may be d
erived by some SCI patients with longstanding injury. The present revi
ew traces the historical development of 4-AP, describes the mechanism
of action and rationale for use in SCI, and provides an overview of th
e clinical trials conducted to date. The early trials give rise to opt
imism that pharmaceutical management of conduction deficits may have a
role to play in restoring neurological function in some patients with
SCI.