Effect of Delayed Administration of U74006F (Tirilazad Mesylate) on Recovery of Locomotor Function After Experimental Spinal Cord Injury
- 1 January 1991
- journal article
- research article
- Published by Mary Ann Liebert Inc in Journal of Neurotrauma
- Vol. 8 (3), 187-192
- https://doi.org/10.1089/neu.1991.8.187
Abstract
Beginning at either 30 minutes, 2 hours, 4 hours, or 8 hours after 180 g compression of the cat L2 spinal cord for 5 minutes, infusion of U74006F was initiated. In this series, the cats received a total U74006F dose of 5 mg/kg/48 hours. An additional group of injured cats was treated at 8 hours postinjury with a three-fold higher dose of U74006F (i.e., a total 48-hour dose of 15 mg/kg). Controls received an equal volume of vehicle (citrate-buffered saline) delivered over 48 hours. The cats were evaluated weekly for 4 weeks for recovery of overground locomotion based on an 11-point scale by an investigator blinded to the time and type (i.e., vehicle or drug) of material administered. By 4 weeks postinjury, there was no significant difference in the locomotor recovery of cats that received U74006F at either 30 minutes, 2 hours, 4 hours, or 8 hours after injury. However, only recovery in the groups treated at 30 minutes, 2 hours, or 4 hours after injury was significantly greater than vehicle-treated controls. Locomotor function in cats receiving either 5 mg/kg/48 hours or 15 mg/kg/48 hours of U74006F at 8 hours postinjury was not significantly different from that of the vehicle-treated animals. Mean (± SEM) 4-week recovery scores were 6.8 ± 0.9, 5.9 ± 1.0, 7.2 ± 1.1, and 4.7 ± 2.9 out of 11 for cats treated at 30 minutes, 2 hours, 4 hours, or 8 hours postinjury, respectively, with the 5 mg/kg/48 hour dose. The mean recovery score for cats treated at 8 hours after injury with the 15 mg/kg/48 hour dose was 3.4 ± 1.8. The average score for the vehicle-treated controls was 1.8 ± 0.8. These findings demonstrate that U74006F can significantly protect locomotor function in our model of compression spinal cord injury if administered as late as 4 hours postinjury. Delaying administration of the compound to 8 hours after injury results in considerable loss of its protective capabilities even if the dose is increased threefold.Keywords
This publication has 23 references indexed in Scilit:
- A Randomized, Controlled Trial of Methylprednisolone or Naloxone in the Treatment of Acute Spinal-Cord InjuryNew England Journal of Medicine, 1990
- Effect of the 21-aminosteroid U-74006F on cerebral vasospasm following subarachnoid hemorrhageJournal of Neurosurgery, 1989
- Protective effect of a 21-aminosteroid on the blood-brain barrier following subarachnoid hemorrhage in rats.Stroke, 1989
- A Trial of the 21-Aminosteroid U74006F in a Primate Model of Chronic Cerebral VasospasmNeurosurgery, 1989
- Effect of the aminosteroid U74006F after cardiopulmonary arrest in dogs.Stroke, 1988
- Effects of the nonglucocorticoid 21-aminosteroid U74006F on acute cerebral hypoperfusion following experimental subarachnoid hemorrhageExperimental Neurology, 1988
- 21-Aminosteroid reduces ion shifts and edema in the rat middle cerebral artery occlusion model of regional ischemia.Stroke, 1988
- 21-Aminosteroid lipid peroxidation inhibitor U74006F protects against cerebral ischemia in gerbils.Stroke, 1988
- Attenuation of postischemic cerebral hypoperfusion by the 21-aminosteroid U74006F.Stroke, 1988
- Pretreatment with Alpha Tocopherol Enhances Neurologic Recovery After Experimental Spinal Cord Compression InjuryJournal of Neurotrauma, 1988