Department of Neurological Surgery, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, People's Republic of China.
Lab Invest. 2012 Nov;92(11):1623-34. doi: 10.1038/labinvest.2012.118. Epub 2012 Sep 10.
The blood-brain barrier (BBB) opening following traumatic brain injury (TBI) provides a chance for therapeutic agents to cross the barrier, yet the reduction of the cerebral microvascular perfusion after TBI may limit the intervention. Meanwhile, optimizing the cerebral capillary perfusion by the strategies such as fluid administration may cause brain edema due to the BBB opening post trauma. To guide the TBI therapy, we characterized the relationship between the changes in the cerebral capillary perfusion and BBB permeability after TBI. First, we observed the changes of the cerebral capillary perfusion by the intracardiac perfusion of Evans Blue and the BBB disruption with magnetic resonance imaging (MRI) in the rat subjected to lateral fluid percussion (FP) brain injury. The correlation between two variables was next evaluated with the correlation analysis. Since related to BBB breakdown, matrix metalloproteinase-9 (MMP-9) activity was finally detected by gelatin zymography. We found that the ratios of the perfused microvessel numbers in the lesioned cortices were significantly reduced at 0 and 1 h post trauma compared with that in the normal cortex, which then dramatically recovered at 4 and 24 h after injury, and that the BBB permeability was greatly augmented in the ipsilateral parts at 4, 12, and 24 h, and in the contralateral area at 24 h after injury compared with that in the uninjured brain. The correlation analysis showed that the BBB permeability increase was related to the restoration of the cerebral capillary perfusion over a 24-h period post trauma. Moreover, the gelatin zymography analysis indicated that the MMP-9 activity in the injured brain increased at 4 h and significantly elevated at 12 and 24 h as compared to that at 0 or 1 h after TBI. Our findings demonstrate that the 4 h post trauma is a critical turning point during the development of TBI, and, importantly, the correlation analysis may guide us how to treat TBI.
创伤性脑损伤(TBI)后血脑屏障(BBB)的开放为治疗药物穿过屏障提供了机会,但 TBI 后大脑微血管灌注的减少可能会限制干预。同时,通过补液等策略优化脑毛细血管灌注可能会因创伤后 BBB 开放而导致脑水肿。为了指导 TBI 治疗,我们研究了 TBI 后大脑毛细血管灌注和 BBB 通透性变化之间的关系。首先,我们通过心脏内灌注 Evans Blue 观察了大鼠在侧方液压冲击(FP)脑损伤后大脑毛细血管灌注的变化和 MRI 显示的 BBB 破坏。然后用相关分析评估两个变量之间的相关性。由于与 BBB 破坏有关,最后通过明胶酶谱法检测基质金属蛋白酶-9(MMP-9)的活性。我们发现,与正常皮质相比,损伤皮质中灌注微血管数量的比值在创伤后 0 和 1 小时明显降低,然后在损伤后 4 和 24 小时急剧恢复,同侧在 4、12 和 24 小时以及对侧在 24 小时后的 BBB 通透性显著增加。相关分析表明,BBB 通透性的增加与创伤后 24 小时内大脑毛细血管灌注的恢复有关。此外,明胶酶谱分析表明,与 TBI 后 0 或 1 小时相比,损伤脑内 MMP-9 活性在 4 小时时增加,并在 12 和 24 小时时显著升高。我们的研究结果表明,创伤后 4 小时是 TBI 发展过程中的一个关键转折点,重要的是,相关分析可以指导我们如何治疗 TBI。