Melgar Miguel A, Rafols Jose, Gloss David, Diaz Fernando G
Department of Neurosurgery, Tulane University School of Medicine, New Orleans, Louisiana 70112, USA.
Neurosurgery. 2005 Mar;56(3):571-81. doi: 10.1227/01.neu.0000154702.23664.3d.
In nonrecovery models of cerebral ischemia, blood-brain barrier (BBB) and cerebral blood flow (CBF) changes are known to occur during reperfusion. It is unknown, however, whether those CBF and BBB alterations occur after brief, transient ischemia with neurological recovery. The purpose of this study was to characterize the time course of CBF and BBB ultrastructural changes during reperfusion in an awake, recovery model of transient global forebrain ischemia (GFI).
Forty-five adult Sprague-Dawley rats were subjected, while awake, to 10 minutes of GFI by the nine-vessel occlusion method. Thirty-five age-matched animals composed a sham-operated group. Normal control (n = 5), sham-operated (n = 5), and nine-vessel occlusion/reperfusion (n = 15) rats were selected for ultrastructural analysis. Electroencephalography was performed, and CBF, mean arterial blood pressure, and intracranial pressure were measured during ischemia and reperfusion up to 24 hours. Quantitative morphological analysis of cortical BBB capillaries was performed by transmission electron microscopy at the same time points at which specific CBF changes occurred during reperfusion.
CBF decreased to 6% of preocclusion values during GFI. This correlated with coma and decerebrate rigidity. During reperfusion, short-lived hyperemia (225 +/- 18%, P < 0.001) was characterized by increased intracranial pressure (28.3 +/- 2.6 mm Hg, P < 0.001) and isoelectric electroencephalogram. This was followed by hypoperfusion, which reached a nadir of 59.7% (59.7 +/- 8.8%, P < 0.01) from baseline by 90 minutes. At this time point, the electroencephalogram recovered, and intracranial pressure and mean arterial blood pressure showed no abnormalities. By 8.5 hours, CBF returned to normal, and this coincided with complete recovery of the animal. Ultrastructural BBB analysis revealed astrocyte end-foot process edema and patent capillaries during hyperemia. Severe interstitial BBB edema and capillary lumen collapse was observed during hypoperfusion. Detachment and migration of pericytes was observed during hypoperfusion and beyond.
A biphasic CBF response is elicited during reperfusion after brief nonlethal GFI under awake conditions.
在脑缺血未恢复模型中,已知血脑屏障(BBB)和脑血流量(CBF)在再灌注期间会发生变化。然而,尚不清楚这些CBF和BBB改变是否会在短暂性、一过性缺血且神经功能恢复后出现。本研究的目的是描述清醒状态下短暂性全脑缺血(GFI)恢复模型再灌注期间CBF和BBB超微结构变化的时间进程。
45只成年Sprague-Dawley大鼠在清醒状态下通过九血管闭塞法接受10分钟的GFI。35只年龄匹配的动物组成假手术组。选择正常对照(n = 5)、假手术(n = 5)和九血管闭塞/再灌注(n = 15)大鼠进行超微结构分析。在缺血和再灌注长达24小时期间进行脑电图检查,并测量CBF、平均动脉血压和颅内压。在再灌注期间特定CBF变化发生的同时时间点,通过透射电子显微镜对皮质BBB毛细血管进行定量形态学分析。
在GFI期间,CBF降至闭塞前值的6%。这与昏迷和去大脑强直相关。在再灌注期间,短暂性充血(225±18%,P < 0.001)的特征是颅内压升高(28.3±2.6 mmHg,P < 0.001)和脑电图等电位。随后是灌注不足,到90分钟时降至基线的最低点59.7%(59.7±8.8%,P < 0.01)。此时,脑电图恢复,颅内压和平均动脉血压无异常。到8.5小时,CBF恢复正常,这与动物的完全恢复同时发生。BBB超微结构分析显示充血期间星形胶质细胞终足水肿和毛细血管通畅。在灌注不足期间观察到严重的间质BBB水肿和毛细血管腔塌陷。在灌注不足期间及之后观察到周细胞的脱离和迁移。
在清醒条件下短暂非致死性GFI后的再灌注期间引发双相CBF反应。