| Literature DB >> 33125600 |
Chengli Liu1, Jie Xie1, Shanshan Sun2, Hui Li1, Tianyu Li1, Chao Jiang3, Xuemei Chen4, Junmin Wang4, Anh Le5, Jiarui Wang6, Zhanfei Li1, Jian Wang7, Wei Wang8.
Abstract
Hemorrhagic transformation (HT) is a common complication after thrombolysis with recombinant tissue-type plasminogen activator (rt-PA) in ischemic stroke. In this article, recent research progress of HT in vivo and in vitro studies was reviewed. We have discussed new potential mechanisms and possible experimental models of HT development, as well as possible biomarkers and treatment methods. Meanwhile, we compared and analyzed rodent models, large animal models and in vitro BBB models of HT, and the limitations of these models were discussed. The molecular mechanism of HT was investigated in terms of BBB disruption, rt-PA neurotoxicity and the effect of neuroinflammation, matrix metalloproteinases, reactive oxygen species. The clinical features to predict HT were represented including blood biomarkers and clinical factors. Recent progress in neuroprotective strategies to improve HT after stroke treated with rt-PA is outlined. Further efforts need to be made to reduce the risk of HT after rt-PA therapy and improve the clinical prognosis of patients with ischemic stroke.Entities:
Keywords: Blood; Brain barrier; Hemorrhagic transformation; Ischemic stroke; Tissue plasminogen activator
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Year: 2020 PMID: 33125600 DOI: 10.1007/s10571-020-00985-1
Source DB: PubMed Journal: Cell Mol Neurobiol ISSN: 0272-4340 Impact factor: 5.046