医学
神经血管束
溶栓
炎症
冲程(发动机)
组织纤溶酶原激活剂
神经炎症
缺血
免疫系统
薄壁组织
脑缺血
微循环
病理
心脏病学
内科学
免疫学
心肌梗塞
机械工程
工程类
作者
Qiang Liu,Kaibin Shi,Yongjun Wang,Fu‐Dong Shi
出处
期刊:Stroke
[Ovid Technologies (Wolters Kluwer)]
日期:2023-09-07
卷期号:54 (10): 2688-2697
被引量:11
标识
DOI:10.1161/strokeaha.123.044123
摘要
Intravenous thrombolysis via tPA (tissue-type plasminogen activator) is the only approved pharmacological treatment for acute ischemic stroke, but its benefits are limited by hemorrhagic transformation. Emerging evidence reveals that tPA swiftly mobilizes immune cells which extravasate into the brain parenchyma via the cerebral vasculature, augmenting neurovascular inflammation, and tissue injury. In this review, we summarize the pronounced alterations of immune cells induced by tPA in patients with stroke and experimental stroke models. We argue that neuroinflammation, triggered by ischemia-induced cell death and exacerbated by tPA, compromises neurovascular integrity and the microcirculation, leading to hemorrhagic transformation. Finally, we discuss current and future approaches to attenuate thrombolysis-associated hemorrhagic transformation via uncoupling immune cells from the neurovascular unit.
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