Little Philip, Kvist Ola, Grankvist Rikard, Jonsson Stefan, Damberg Peter, Söderman Michael, Arnberg Fabian, Holmin Staffan
Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Department of Neuroradiology, Karolinska University Hospital, Solna, Stockholm, Sweden.
PLoS One. 2017 Jan 9;12(1):e0169541. doi: 10.1371/journal.pone.0169541. eCollection 2017.
Interventional treatment regimens have increased the demand for accurate understanding of the progression of injury in acute ischemic stroke. However, conventional animal models severely inhibit collateral blood flow and mimic the malignant infarction profile not suitable for treatment. The aim of this study was to provide a clinically relevant profile of the emergence and course of ischemic injury in cases suitable for acute intervention, and was achieved by employing a M2 occlusion model (M2CAO) that more accurately simulates middle cerebral artery (MCA) occlusion in humans. Twenty-five Sprague-Dawley rats were subjected to Short (90 min), Intermediate (180 min) or Extended (600 min) transient M2CAO and examined longitudinally with interleaved diffusion-, T2- and arterial spin labeling perfusion-weighted magnetic resonance imaging before and after reperfusion. We identified a rapid emergence of cytotoxic edema within tissue regions undergoing infarction, progressing in several distinct phases in the form of subsequent moderation and then reversal at 230 min (p < 0.0001). We identified also the early emergence of vasogenic edema, which increased consistently before and after reperfusion (p < 0.0001). The perfusion of the penumbra correlated more strongly to the perfusion of adjacent tissue regions than did the perfusion of regions undergoing infarction (p = 0.0088). This was interpreted as an effect of preserved collateral blood flow during M2CAO. Accordingly, we observed only limited recruitment of penumbra regions to the infarction core. However, a gradual increase in infarction size was still occurring as late as 10 hours after M2CAO. Our results indicate that patients suffering MCA branch occlusion stand to benefit from interventional therapy for an extended time period after the emergence of ischemic injury.
介入治疗方案增加了准确了解急性缺血性中风损伤进展情况的需求。然而,传统动物模型严重抑制侧支血流,模拟出的恶性梗死情况不适合治疗。本研究的目的是提供适合急性干预病例中缺血性损伤出现及过程的临床相关情况,通过采用更准确模拟人类大脑中动脉(MCA)闭塞的M2闭塞模型(M2CAO)得以实现。25只Sprague-Dawley大鼠接受了短期(90分钟)、中期(180分钟)或长期(600分钟)的短暂M2CAO,并在再灌注前后通过交错的扩散加权、T2加权和动脉自旋标记灌注加权磁共振成像进行纵向检查。我们发现在发生梗死的组织区域内细胞毒性水肿迅速出现,以几个不同阶段进展,随后在230分钟时缓解然后逆转(p < 0.0001)。我们还发现血管源性水肿早期出现,在再灌注前后持续增加(p < 0.0001)。半暗带的灌注与相邻组织区域的灌注相关性比梗死区域的灌注更强(p = 0.0088)。这被解释为M2CAO期间侧支血流得以保留的结果。因此,我们仅观察到半暗带区域有限地向梗死核心发展。然而,直到M2CAO后10小时梗死面积仍在逐渐增加。我们的结果表明,患有MCA分支闭塞的患者在缺血性损伤出现后较长时间内可能从介入治疗中获益。