Headache Research and Treatment Program, Department of Neurology, David Geffen School of Medicine at UCLA, 635 Charles E. Young Drive South, Neuroscience Research Building 1, Room 555a, Los Angeles, CA 90095, USA.
Brain. 2010 Apr;133(Pt 4):996-1012. doi: 10.1093/brain/awp338. Epub 2010 Mar 25.
Cortical spreading depression is a propagating wave of depolarization that plays important roles in migraine, stroke, subarachnoid haemorrhage and brain injury. Cortical spreading depression is associated with profound vascular changes that may be a significant factor in the clinical response to cortical spreading depression events. We used a combination of optical intrinsic signal imaging, electro-physiology, potassium sensitive electrodes and spectroscopy to investigate neurovascular changes associated with cortical spreading depression in the mouse. We identified two distinct phases of altered neurovascular function, one during the propagating cortical spreading depression wave and a second much longer phase after passage of the wave. The direct current shift associated with the cortical spreading depression wave was accompanied by marked arterial constriction and desaturation of cortical haemoglobin. After recovery from the initial cortical spreading depression wave, we observed a second phase of prolonged, negative direct current shift, arterial constriction and haemoglobin desaturation, lasting at least an hour. Persistent disruption of neurovascular coupling was demonstrated by a loss of coherence between electro-physiological activity and perfusion. Extracellular potassium concentration increased during the cortical spreading depression wave, but recovered and remained at baseline after passage of the wave, consistent with different mechanisms underlying the first and second phases of neurovascular dysfunction. These findings indicate that cortical spreading depression is associated with a multiphasic alteration in neurovascular function, including a novel second direct current shift accompanied by arterial constriction and decrease in tissue oxygen supply, that is temporally and mechanistically distinct from the initial propagated cortical spreading depression wave. Vascular/metabolic uncoupling with cortical spreading depression may have important clinical consequences, and the different phases of dysfunction may represent separate therapeutic targets in the disorders where cortical spreading depression occurs.
皮层扩散性抑制是一种去极化传播波,在偏头痛、中风、蛛网膜下腔出血和脑损伤中发挥重要作用。皮层扩散性抑制与深刻的血管变化有关,这些变化可能是皮层扩散性抑制事件临床反应的一个重要因素。我们使用光学固有信号成像、电生理学、钾敏电极和光谱学的组合来研究与小鼠皮层扩散性抑制相关的神经血管变化。我们确定了与皮层扩散性抑制相关的神经血管功能的两个不同阶段,一个在传播的皮层扩散性抑制波期间,另一个在波通过后很长一段时间。与皮层扩散性抑制波相关的直流偏移伴随着明显的动脉收缩和皮质血红蛋白的去饱和。在从初始皮层扩散性抑制波恢复后,我们观察到第二个相位的长时间、负直流偏移、动脉收缩和血红蛋白去饱和,持续至少一个小时。神经血管偶联的持续中断通过电生理活动和灌注之间的相干性丧失来证明。在皮层扩散性抑制波期间,细胞外钾浓度增加,但在波通过后恢复并保持在基线,这与神经血管功能障碍的第一和第二阶段的不同机制一致。这些发现表明,皮层扩散性抑制与神经血管功能的多相改变有关,包括与初始传播的皮层扩散性抑制波在时间和机制上不同的新型第二直流偏移,伴有动脉收缩和组织氧供应减少。皮层扩散性抑制与血管/代谢解偶联可能具有重要的临床后果,并且功能障碍的不同阶段可能代表皮层扩散性抑制发生的疾病中的单独治疗靶点。