The present work was performed to establish whether pre-injury adminis
tration of the 27-Aminosteroid, U-74389F, is beneficial for treatment
of acute spinal cord trauma in rats, as it has been demonstrated that
the bolus administration of the same compound one hour after injury fa
cilitates the return of the spinal cord function as measured by electr
ophysiological recordings in this compression animal model of spinal c
ord trauma. Cortical somatosensory evoked potentials (CSSEPs) were rec
orded as an indicator of spinal cord function before and after a sever
e compression injury. Vital signs and the CSSEPs were monitored up to
five hours post-injury. U-4389F treatment was given as a single inject
ion (15 mg kg(-1)) one hour prior to the injury which was followed by
a continuous infusion (3 mg kg(-1) h(-1)) during the procedure. The CS
SEPs were abolished immediately after this injury both, in the untreat
ed and treated animal groups. The majority of the treated animals (80%
) demonstrated recovery of the CSSEPs within the second hour post-inju
ry. The control group showed 40% recovery at this time period. At five
hours post-injury, recovery rates were 47% and 87% for control and tr
eated groups respectively. We conclude that the administration of the
21-Aminosteroid, U74389F, one hour prior to spinal cord injury facilit
ates the return of spinal cord function as measured by CSSEPs in a com
pression rat model of acute spinal cord trauma, supporting and verifyi
ng our previous experiences using the same compound as i.v. bolus inje
ctions one, two and three hours after the trauma, respectively.