Department of Biomedicine Aarhus University Aarhus Denmark.
Neurophotonics Center, Department of Biomedical Engineering Boston University Boston MA USA.
J Am Heart Assoc. 2023 Jun 6;12(11):e029527. doi: 10.1161/JAHA.123.029527. Epub 2023 May 26.
Background Normal brain function depends on the ability of the vasculature to increase blood flow to regions with high metabolic demands. Impaired neurovascular coupling, such as the local hyperemic response to neuronal activity, may contribute to poor neurological outcome after stroke despite successful recanalization, that is, futile recanalization. Methods and Results Mice implanted with chronic cranial windows were trained for awake head-fixation before experiments. One-hour occlusion of the anterior middle cerebral artery branch was induced using single-vessel photothrombosis. Cerebral perfusion and neurovascular coupling were assessed by optical coherence tomography and laser speckle contrast imaging. Capillaries and pericytes were studied in perfusion-fixed tissue by labeling lectin and platelet-derived growth factor receptor β. Arterial occlusion induced multiple spreading depolarizations over 1 hour associated with substantially reduced blood flow in the peri-ischemic cortex. Approximately half of the capillaries in the peri-ischemic area were no longer perfused at the 3- and 24-hour follow-up (45% [95% CI, 33%-58%] and 53% [95% CI, 39%-66%] reduction, respectively; <0.0001), which was associated with contraction of an equivalent proportion of peri-ischemic capillary pericytes. The capillaries in the peri-ischemic cortex that remained perfused showed increased point prevalence of dynamic flow stalling (0.5% [95% CI, 0.2%-0.7%] at baseline, 5.1% [95% CI, 3.2%-6.5%] and 3.2% [95% CI, 1.1%-5.3%] at 3- and 24-hour follow-up, respectively; =0.001). Whisker stimulation at the 3- and 24-hour follow-up led to reduced neurovascular coupling responses in the sensory cortex corresponding to the peri-ischemic region compared with that observed at baseline. Conclusions Arterial occlusion led to contraction of capillary pericytes and capillary flow stalling in the peri-ischemic cortex. Capillary dysfunction was associated with neurovascular uncoupling. Neurovascular coupling impairment associated with capillary dysfunction may be a mechanism that contributes to futile recanalization. Hence, the results from this study suggest a novel treatment target to improve neurological outcome after stroke.
背景 正常的大脑功能依赖于血管增加血流以满足高代谢需求的能力。神经血管耦联受损,如神经元活动引起的局部充血反应,可能导致尽管成功再通(即无效再通),但卒中后神经功能预后不良。
方法和结果 实验前,通过慢性颅窗植入的小鼠接受了清醒头部固定训练。使用单血管光血栓形成诱导前中脑动脉分支 1 小时闭塞。通过光相干断层扫描和激光散斑对比成像评估脑灌注和神经血管耦联。通过标记凝集素和血小板衍生生长因子受体 β 研究灌注固定组织中的毛细血管和周细胞。动脉闭塞诱导了 1 小时内的多个弥散性去极化,导致缺血皮质的血流显著减少。在 3 小时和 24 小时的随访中,缺血区约一半的毛细血管不再灌注(分别为 45%[95%CI,33%-58%]和 53%[95%CI,39%-66%]减少,<0.0001),这与缺血周细胞的等效比例收缩相关。缺血皮质中保持灌注的毛细血管显示出动态血流停滞的点患病率增加(在基线时为 0.5%[95%CI,0.2%-0.7%],在 3 小时和 24 小时随访时分别为 5.1%[95%CI,3.2%-6.5%]和 3.2%[95%CI,1.1%-5.3%];=0.001)。在 3 小时和 24 小时随访时,与基线相比,胡须刺激导致感觉皮层中与缺血区相应的神经血管耦联反应降低。
结论 动脉闭塞导致缺血皮质中毛细血管周细胞收缩和毛细血管血流停滞。毛细血管功能障碍与神经血管解耦联有关。与毛细血管功能障碍相关的神经血管耦联受损可能是导致无效再通的机制之一。因此,这项研究的结果表明了一种改善卒中后神经功能预后的新治疗靶点。