Chi Oak Z, Barsoum Sylviana, Rah Kang H, Liu Xia, Weiss Harvey R
Department of Anesthesiology, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey.
Department of Anesthesiology, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey.
J Stroke Cerebrovasc Dis. 2015 Jun;24(6):1196-203. doi: 10.1016/j.jstrokecerebrovasdis.2015.01.016. Epub 2015 Apr 11.
Most anesthetics affect cerebral blood flow and metabolism. We compared microregional O2 balance in cerebral ischemia-reperfusion during pentobarbital and isoflurane anesthesia.
After 1 hour of middle cerebral artery occlusion and a 2-hour reperfusion under isoflurane (1.4%, n = 14) or pentobarbital (50 mg/kg, n = 14) anesthesia in rats, regional cerebral blood flow using (14)C-iodoantipyrine autoradiography, microregional arterial and venous O2 saturation (20-60 μm in diameter) using cryomicrospectrophotometry, and the size of cortical infarct were determined.
Ischemia-reperfusion decreased the average cortical venous O2 saturation in both pentobarbital and isoflurane groups (P < .0001), which was higher (P < .05) with pentobarbital despite a similar average regional cerebral blood flow and O2 consumption. The heterogeneity of venous O2 saturation reported as a coefficient of variation (100 × standard deviation/mean) was smaller (P < .005) with pentobarbital than that with isoflurane (7.5 versus 16.1). The number of veins with low venous O2 saturation (<50%) was smaller (P < .005) with pentobarbital (5 of 80 versus 24 of 80). The percentage of cortical infarct in total cortex was smaller with pentobarbital (5.2 ± 2.5% versus 12.3 ± 2.6%, P < .001).
In the cerebral ischemic-reperfused cortex, the average venous O2 saturation was higher, and its heterogeneity and the number of veins with low O2 saturation were smaller under pentobarbital than isoflurane anesthesia. This improvement in microregional O2 balance with pentobarbital was accompanied by the reduced cortical infarct. Our data suggest that the neurologic outcome could vary during cerebral ischemia-reperfusion depending on the anesthetics used.
大多数麻醉药会影响脑血流量和代谢。我们比较了戊巴比妥和异氟烷麻醉期间脑缺血再灌注时的微区氧平衡。
在大鼠大脑中动脉闭塞1小时并在异氟烷(1.4%,n = 14)或戊巴比妥(50 mg/kg,n = 14)麻醉下再灌注2小时后,使用(14)C-碘安替比林放射自显影术测定局部脑血流量,使用低温显微分光光度法测定微区动脉和静脉氧饱和度(直径20 - 60μm),并确定皮质梗死灶大小。
缺血再灌注使戊巴比妥组和异氟烷组的平均皮质静脉氧饱和度均降低(P <.0001),尽管平均局部脑血流量和氧消耗相似,但戊巴比妥组的平均皮质静脉氧饱和度更高(P <.05)。以变异系数(100×标准差/均值)表示的静脉氧饱和度异质性,戊巴比妥组比异氟烷组小(P <.)。戊巴比妥组氧饱和度低(<50%)的静脉数量更少(P <.)。戊巴比妥组皮质梗死灶占总皮质的百分比更小(5.2±2.5%对12.3±2.6%,P <.001)。
在脑缺血再灌注皮质中,戊巴比妥麻醉下的平均静脉氧饱和度更高,其异质性和氧饱和度低的静脉数量比异氟烷麻醉时更小。戊巴比妥对微区氧平衡的这种改善伴随着皮质梗死灶的减少。我们的数据表明,在脑缺血再灌注期间,神经学结果可能因所用麻醉药而异。