Baker C J, Onesti S T, Solomon R A
Department of Neurological Surgery, Columbia-Presbyterian Medical Center, Columbia University College of Physicians and Surgeons, New York, New York.
J Neurosurg. 1992 Sep;77(3):438-44. doi: 10.3171/jns.1992.77.3.0438.
The effect of hypothermia on neuronal injury following permanent middle cerebral artery (MCA) occlusion in the rat was examined. Moderate hypothermia (body temperature 24 degrees C) was induced before MCA occlusion (0-minute delay group) in six rats, at 30 minutes in eight rats, and at 1 (seven rats), 2 (seven rats), and 3 (nine rats) hours after occlusion. The rats were kept at a 24 degrees C body temperature for 1 hour, then allowed to rewarm over 90 minutes. The animals were sacrificed 24 hours after MCA occlusion, and infarction was visualized by staining of coronal sections with 2,3,5-triphenyltetrazolium chloride. Infarct volumes were compared to matched normothermic control rats (body temperature 36 degrees C). Additional groups of 0-minute delay hypothermic (10 rats) and control animals (nine rats) were sacrificed 72 hours after MCA occlusion to examine the effects of prolonged survival. A significant reduction in the percentage of infarcted right hemisphere was seen in the animals sacrificed after 24 hours with 0-minute, 30-minute, and 1-hour delays in inducing hypothermia (mean +/- standard error of the mean: 2.2% +/- 0.7%, 4.4% +/- 0.9%, and 3.6% +/- 1.1%, respectively) as compared to normothermic control rats (10.8% +/- 1.5%, p less than 0.01 by Student's t-test). In the 2- and 3-hour delay groups, the percentage of infarcted right hemisphere was 17.1% +/- 2.4% and 12.0% +/- 2.7%, respectively, and no decrease in infarct volume was observed. The 0-minute delay hypothermia group sacrificed after 72 hours also displayed a significant reduction in right hemisphere infarct compared to their respective controls (4.8% vs. 11.7%, p less than 0.05). These findings indicate that, in the setting of permanent MCA occlusion, hypothermia markedly decreases brain injury even when its induction is delayed for up to 1 hour after the onset of ischemia. Ischemic damage does not appear to be merely retarded but permanently averted.
研究了低温对大鼠大脑中动脉(MCA)永久性闭塞后神经元损伤的影响。在六只大鼠MCA闭塞前(0分钟延迟组)、八只大鼠在闭塞后30分钟、七只大鼠在闭塞后1小时、七只大鼠在闭塞后2小时以及九只大鼠在闭塞后3小时诱导中度低温(体温24摄氏度)。将大鼠维持在24摄氏度体温1小时,然后在90分钟内使其复温。在MCA闭塞24小时后处死动物,用2,3,5-氯化三苯基四氮唑对冠状切片进行染色以观察梗死情况。将梗死体积与匹配的正常体温对照大鼠(体温36摄氏度)进行比较。另外,在MCA闭塞72小时后处死0分钟延迟低温组(10只大鼠)和对照组动物(9只大鼠)以研究延长存活时间的影响。与正常体温对照大鼠相比,在诱导低温延迟0分钟、30分钟和1小时后24小时处死的动物中,梗死右半球的百分比显著降低(平均值±平均标准误差:分别为2.2%±0.7%、4.4%±0.9%和3.6%±1.1%),而正常体温对照大鼠为10.8%±1.5%,经学生t检验p<0.01)。在2小时和3小时延迟组中,梗死右半球的百分比分别为17.1%±2.4%和12.0%±2.7%,未观察到梗死体积减小。在72小时后处死的0分钟延迟低温组与各自对照组相比,右半球梗死也显著降低(4.8%对11.7%,p<0.05)。这些发现表明,在永久性MCA闭塞的情况下,即使在缺血发作后长达1小时延迟诱导低温,低温也能显著减少脑损伤。缺血损伤似乎并非仅仅被延迟,而是被永久避免。