Department of Neurology and Center for Translational Neuro- and Behavioral Sciences (C-TNBS), University Hospital Essen, Hufelandstr. 55, D-45147, Essen, Germany.
Department of Pharmacology & Personalized Medicine, MeHNS, Faculty of Health, Medicine & Life Science, Maastricht University, Maastricht, The Netherlands.
J Neuroinflammation. 2024 Jun 13;21(1):155. doi: 10.1186/s12974-024-03149-w.
Activation of the kallikrein-kinin system promotes vascular leakage, inflammation, and neurodegeneration in ischemic stroke. Inhibition of plasma kallikrein (PK) - a key component of the KKS - in the acute phase of ischemic stroke has been reported to reduce thrombosis, inflammation, and damage to the blood-brain barrier. However, the role of PK during the recovery phase after cerebral ischemia is unknown. To this end, we evaluated the effect of subacute PK inhibition starting from day 3 on the recovery process after transient middle artery occlusion (tMCAO). Our study demonstrated a protective effect of PK inhibition by reducing infarct volume and improving functional outcome at day 7 after tMCAO. In addition, we observed reduced thrombus formation in cerebral microvessels, fewer infiltrated immune cells, and an improvement in blood-brain barrier integrity. This protective effect was facilitated by promoting tight junction reintegration, reducing detrimental matrix metalloproteinases, and upregulating regenerative angiogenic markers. Our findings suggest that PK inhibition in the subacute phase might be a promising approach to accelerate the post-stroke recovery process.
激肽释放酶-激肽系统的激活会促进缺血性中风中的血管渗漏、炎症和神经退行性变。在缺血性中风的急性期抑制血浆激肽释放酶(PK)——激肽释放酶系统的关键组成部分——已被报道可减少血栓形成、炎症和血脑屏障损伤。然而,PK 在脑缺血后恢复阶段的作用尚不清楚。为此,我们评估了从第 3 天开始的亚急性 PK 抑制对短暂性大脑中动脉闭塞(tMCAO)后恢复过程的影响。我们的研究表明,PK 抑制通过减少梗塞体积和改善 tMCAO 后第 7 天的功能结果来发挥保护作用。此外,我们观察到脑微血管中的血栓形成减少,浸润的免疫细胞减少,血脑屏障完整性得到改善。这种保护作用是通过促进紧密连接的重新整合、减少有害的基质金属蛋白酶和上调再生血管生成标志物来实现的。我们的研究结果表明,亚急性期的 PK 抑制可能是一种有前途的方法,可以加速中风后的恢复过程。