Stroke Diagnostics and Therapeutics Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892, USA.
J Cereb Blood Flow Metab. 2010 Jun;30(6):1188-99. doi: 10.1038/jcbfm.2010.1. Epub 2010 Mar 3.
In this study, we examined the relationship between tissue and blood levels of matrix metalloproteinase (MMP)-2 and MMP-9 through gelatin zymography at multiple time points after experimental stroke. We additionally investigated the association between these levels and the evidence of blood-cerebrospinal fluid (CSF) barrier (BCSFB) and blood-brain barrier (BBB) disruption on post-contrast fluid-attenuated inversion-recovery (FLAIR) imaging. Increased plasma MMP-9 was associated with BCSFB disruption at 1h post-reperfusion. Ventricular enhancement ipsilateral to the stroke was 500+/-100%, significantly higher than sham, 24, and 48 h groups. Increased tissue MMP-2 and MMP-9 were associated with BBB disruption at 48 h post-reperfusion. Parenchymal enhancement was 60+/-20% for a volume equivalent to 260+/-80 mm(3). Although the percent enhancement was comparable across groups, the volume of enhancing lesion was significantly higher at 48 h (260+/-80 mm(3), 100%) in comparison to 1 h (8+/-3 mm(3), 3%) and 24 h (51 mm(3), 18%). These findings support the use of imaging markers of BCSFB and BBB status as indirect measures of MMP regulation in the blood and brain tissue. The methods presented herein should be useful in understanding the link between MMPs, barrier integrity, and subsequent hemorrhagic transformation.
在本研究中,我们通过明胶酶谱法在实验性中风后多个时间点检测了组织和血液中基质金属蛋白酶(MMP)-2 和 MMP-9 之间的关系。我们还研究了这些水平与血脑屏障(BBB)和血脑脊液屏障(BCSFB)破坏的证据之间的相关性,这种破坏在对比后流体衰减反转恢复(FLAIR)成像上表现出来。再灌注后 1 小时,血浆 MMP-9 的增加与 BCSFB 破坏有关。中风同侧脑室增强为 500+/-100%,明显高于假手术组、24 小时组和 48 小时组。再灌注后 48 小时组织 MMP-2 和 MMP-9 的增加与 BBB 破坏有关。实质增强为 60+/-20%,相当于 260+/-80mm(3)的体积。尽管各组的增强百分比相当,但在 48 小时(260+/-80mm(3),100%)的增强病变体积明显高于 1 小时(8+/-3mm(3),3%)和 24 小时(51mm(3),18%)。这些发现支持使用 BCSFB 和 BBB 状态的成像标志物作为血液和脑组织中 MMP 调节的间接指标。本文提出的方法应有助于理解 MMPs、屏障完整性与随后的出血性转化之间的联系。