No long-term benefit from hypothermia after severe traumatic brain injury with secondary insult in rats

Citation
Cl. Robertson et al., No long-term benefit from hypothermia after severe traumatic brain injury with secondary insult in rats, CRIT CARE M, 28(9), 2000, pp. 3218-3223
Citations number
38
Categorie Soggetti
Aneshtesia & Intensive Care
Journal title
CRITICAL CARE MEDICINE
ISSN journal
00903493 → ACNP
Volume
28
Issue
9
Year of publication
2000
Pages
3218 - 3223
Database
ISI
SICI code
0090-3493(200009)28:9<3218:NLBFHA>2.0.ZU;2-K
Abstract
Objectives: To evaluate the effect of application of transient, moderate hy pothermia on outcome after experimental traumatic brain injury (TBI) with a secondary hypoxemic insult. Design: Prospective, randomized study. Setting: University-based animal research facility. Subjects: Male Sprague- Dawley rats. Interventions: All rats were subjected to severe TBI followed by 30 mins of moderate hypoxemia, associated with mild hypotension. Rats were randomized to three groups: a) normothermia (37 degrees C +/- 0.5 degrees C); b) imme diate hypothermia (32 degrees C +/- 0.5 degrees C initiated after trauma, b efore hypoxemia); and c) delayed hypothermia (32 degrees C +/- 0.5 degrees C after hypoxemia), The brain temperature was controlled for 4 hrs after TB I and hypoxemia, Measurements and Main Results: Animals were evaluated after TBI for motor a nd cognitive performance using beam balance (days 1-5 after TBI), beam walk ing (days 1-5 after TBI), and Morris Water Maze (days 14-18 after TBI) asse ssments, On day 21 after TBI, rats were perfused with paraformaldehyde and brains were histologically evaluated for lesion volume and hippocampal neur on counts. All three groups showed marked deficits in beam balance, beam wa lking, and Morris Water Maze performance. However, these deficits did not d iffer between groups. There was no difference in lesion volume between grou ps. All animals had significant hippocampal neuronal loss on the side ipsil ateral to injury, but this loss was similar between groups. Conclusions:ln this rat model of severe TBI with secondary insult, moderate hypothermia for 4 hrs posttrauma failed to improve motor function, cogniti ve function, lesion volume or hippocampal neuronal survival. Combination th erapies may be necessary in this difficult setting.