Secondary Insults Increase Injury after Controlled Cortical Impact in Rats
- 1 July 1996
- journal article
- Published by Mary Ann Liebert Inc in Journal of Neurotrauma
- Vol. 13 (7) , 371-383
- https://doi.org/10.1089/neu.1996.13.371
Abstract
Secondary ischemic insults are common after severe head injury and contribute to poor neurological outcome. To study the increased vulnerability of the traumatized brain to secondary insults, bilateral carotid occlusion was produced after a controlled cortical impact injury in rats. The injury produced by either the impact injury or the bilateral carotid occlusion was mild to moderate when studied individually. The 1 and 3 m/sec impact injuries alone caused no detectable contusion at the impact side and minimal neuronal loss in the hippocampus. The 5 m/sec impact injury alone resulted in a small contusion with a median volume of 5.4 mm3. The 40-min period of bilateral carotid occlusion alone caused no cortical injury and no neuronal loss in the CA1 region of the hippocampus. When the 40 min of bilateral carotid occlusion was produced 1 h after the impact injury, there was an increase in the damage produced. The contusion volume was significantly larger after the 3 and 5 m/sec impact injuries and the hippocampal neuronal loss was significantly greater after the 1 and 3 m/sec impact injuries. When varying durations of bilateral carotid occlusion were produced 1 h after a 3 m/sec impact injury, contusion volume was significantly larger after bilateral carotid occlusion duration of 40 min, and CA1 neuronal loss was significantly greater after bilateral carotid occlusion durations of 30 and 40 min. When 40 min of bilateral carotid occlusion was produced at different time intervals after a 3 m/sec injury, the increased contusion volume was maximal when bilateral carotid occlusion occurred at 4 h after the impact injury, and the increased neuronal loss in the CA3 region of the hippocampus was maximal when bilateral carotid occlusion occurred at 1 h after the impact injury. By 24 h after the impact injury, 40 min of bilateral carotid occlusion had minimal consequences, similar to the effect in sham-injured animals. These results mimic the clinical situation where secondary insults of a severity that would not cause permanent neurological damage in a normal person are associated with a marked worsening of neurological outcome after head injury and where the injured brain is most susceptible to secondary insults in the first few hours after injury.Keywords
This publication has 25 references indexed in Scilit:
- Lateral Cortical Impact Injury in Rats: Pathologic Effects of Varying Cortical Compression and Impact VelocityJournal of Neurotrauma, 1994
- Lateral Cortical Impact Injury in Rats: Cerebrovascular Effects of Varying Depth of Cortical Deformation and Impact VelocityJournal of Neurotrauma, 1994
- Jugular venous desaturation and outcome after head injury.Journal of Neurology, Neurosurgery & Psychiatry, 1994
- THE ROLE OF SECONDARY BRAIN INJURY IN DETERMINING OUTCOME FROM SEVERE HEAD INJURYPublished by Wolters Kluwer Health ,1993
- Ultra-early evaluation of regional cerebral blood flow in severely head-injured patients using xenon-enhanced computerized tomographyJournal of Neurosurgery, 1992
- The effect of changes in cerebral perfusion pressure upon middle cerebral artery blood flow velocity and jugular bulb venous oxygen saturation after severe brain injuryJournal of Neurosurgery, 1992
- Reduced cerebral blood flow, oxygen delivery, and electroencephalographic activity after traumatic brain injury and mild hemorrhage in catsJournal of Neurosurgery, 1992
- Restoration of cerebrovascular responsiveness to hyperventilation by the oxygen radical scavenger n-acetylcysteine following experimental traumatic brain injuryJournal of Neurosurgery, 1991
- Recovery of impaired endothelium-dependent relaxation after fluid-percussion brain injury in cats.Stroke, 1989
- Autoregulation and CO2 responses of cerebral blood flow in patients with acute severe head injuryJournal of Neurosurgery, 1978