Henninger Nils, Sicard Kenneth M, Schmidt Karl F, Bardutzky Jürgen, Fisher Marc
Department of Neurology, University of Massachusetts Medical School, Worcester, MA 01604, USA.
Stroke. 2006 May;37(5):1283-7. doi: 10.1161/01.STR.0000217223.72193.98. Epub 2006 Mar 23.
Differences among models in the temporal evolution of ischemia after middle cerebral artery occlusion (MCAO) in rats may considerably influence the results of experimental stroke research. Using diffusion and perfusion imaging, we compared the spatiotemporal evolution of ischemia in Sprague Dawley rats after permanent suture MCAO (sMCAO; n=8) and embolic MCAO (eMCAO; n=8).
Serial measurements of quantitative cerebral blood flow (CBF) and the apparent diffusion coefficient (ADC) were performed up to 180 minutes after MCAO. ADC and CBF values within 5 different brain regions were analyzed. ADC and CBF lesion volumes were calculated by using previously established viability thresholds and correlated with infarct volume defined by 2,3,5-triphenyltetrazolium chloride staining 24 hours after MCAO.
Compared with sMCAO animals, the threshold-derived CBF lesion volume was significantly larger in eMCAO at all time points (P<0.01), remained relatively constant over time, and was highly correlated with the 2,3,5-triphenyltetrazolium chloride-defined infarct size. The ADC lesion volume did not differ between models at any time point. A diffusion/perfusion mismatch was present significantly longer in eMCAO animals (P<0.05), and these rats demonstrated larger absolute mismatch volumes that were statistically significant at 30, 60, and 90 minutes (P<0.05). In both models, CBF and ADC declines were highly correlated.
This study demonstrated substantial differences in acute ischemic lesion evolution between the eMCAO and sMCAO models.
大鼠大脑中动脉闭塞(MCAO)后缺血的时间演变模型之间的差异可能会对实验性中风研究的结果产生重大影响。我们使用扩散和灌注成像,比较了永久性缝合MCAO(sMCAO;n = 8)和栓塞性MCAO(eMCAO;n = 8)后Sprague Dawley大鼠缺血的时空演变。
在MCAO后长达180分钟内对定量脑血流量(CBF)和表观扩散系数(ADC)进行连续测量。分析了5个不同脑区的ADC和CBF值。通过使用先前确定的存活阈值计算ADC和CBF病变体积,并将其与MCAO后24小时用2,3,5-三苯基四氮唑氯化物染色定义的梗死体积相关联。
与sMCAO动物相比,eMCAO在所有时间点的阈值衍生CBF病变体积均显著更大(P<0.01),随时间保持相对恒定,并且与2,3,5-三苯基四氮唑氯化物定义的梗死大小高度相关。在任何时间点,模型之间的ADC病变体积均无差异。eMCAO动物中扩散/灌注不匹配存在的时间明显更长(P<0.05),并且这些大鼠表现出更大的绝对不匹配体积,在30、60和90分钟时具有统计学意义(P<0.05)。在两种模型中,CBF和ADC的下降高度相关。
本研究表明eMCAO和sMCAO模型在急性缺血性病变演变方面存在实质性差异。