Rivaroxaban does not influence hemorrhagic transformation in a diabetes ischemic stroke and endovascular thrombectomy model

Abstract Managing endovascular thrombectomy (ET) in diabetic ischemic stroke (IS) with novel anticoagulants is challenging due to putative risk of intracerebral hemorrhage. The study evaluates increased hemorrhagic transformation (HT) risk in Rivaroxaban-treated diabetic rats post ET. Diabetes was i...

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Autores principales: Feng-Di Liu, Rong Zhao, Xiao-Yan Feng, Yan-Hui Shi, Yi-Lan Wu, Xiao-Lei Shen, Ge-Fei Li, Yi-Sheng Liu, Ying Zhao, Xin-Wei He, Jia-Wen Yin, Mei-Ting Zhuang, Bing-Qiao Zhao, Jian-Ren Liu
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Publicado: Nature Portfolio 2018
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spelling oai:doaj.org-article:e9ecc3c70b3b418989989d7058ee0d7d2021-12-02T15:09:07ZRivaroxaban does not influence hemorrhagic transformation in a diabetes ischemic stroke and endovascular thrombectomy model10.1038/s41598-018-25820-y2045-2322https://doaj.org/article/e9ecc3c70b3b418989989d7058ee0d7d2018-05-01T00:00:00Zhttps://doi.org/10.1038/s41598-018-25820-yhttps://doaj.org/toc/2045-2322Abstract Managing endovascular thrombectomy (ET) in diabetic ischemic stroke (IS) with novel anticoagulants is challenging due to putative risk of intracerebral hemorrhage. The study evaluates increased hemorrhagic transformation (HT) risk in Rivaroxaban-treated diabetic rats post ET. Diabetes was induced in male Sprague-Dawley rats by intraperitoneal injection of 60 mg/kg streptozotocin. After 4-weeks, rats were pretreated orally with 30 mg/kg Rivaroxaban/saline; prothrombin time was monitored. IS and ET was induced after 1 h, by thread-induced transient middle cerebral artery occlusion (tMCAO) that mimicked mechanical ET for proximal MCA occlusion at 60 min. After 24 h reperfusion, infarct volumes, HT, blood-brain barrier (BBB) permeability, tight junction at peri-ischemic lesion and matrix metalloproteinase-9 (MMP-9) activity was measured. Diabetic rats seemed to exhibit increased infarct volume and HT at 24 h after ET than normal rats. Infarct volumes and functional outcomes did not differ between Rivaroxaban and diabetic control groups. A significant increase in HT volumes and BBB permeability under Rivaroxaban treatment was not detected. Compared to diabetic control group, neither the occludin expression was remarkably lower in the Rivaroxaban group nor the MMP-9 activity was higher. Together, Rivaroxaban does not increase HT after ET in diabetic rats with proximal MCA occlusion, since Rivaroxaban has fewer effects on post-ischemic BBB permeability.Feng-Di LiuRong ZhaoXiao-Yan FengYan-Hui ShiYi-Lan WuXiao-Lei ShenGe-Fei LiYi-Sheng LiuYing ZhaoXin-Wei HeJia-Wen YinMei-Ting ZhuangBing-Qiao ZhaoJian-Ren LiuNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 8, Iss 1, Pp 1-9 (2018)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Feng-Di Liu
Rong Zhao
Xiao-Yan Feng
Yan-Hui Shi
Yi-Lan Wu
Xiao-Lei Shen
Ge-Fei Li
Yi-Sheng Liu
Ying Zhao
Xin-Wei He
Jia-Wen Yin
Mei-Ting Zhuang
Bing-Qiao Zhao
Jian-Ren Liu
Rivaroxaban does not influence hemorrhagic transformation in a diabetes ischemic stroke and endovascular thrombectomy model
description Abstract Managing endovascular thrombectomy (ET) in diabetic ischemic stroke (IS) with novel anticoagulants is challenging due to putative risk of intracerebral hemorrhage. The study evaluates increased hemorrhagic transformation (HT) risk in Rivaroxaban-treated diabetic rats post ET. Diabetes was induced in male Sprague-Dawley rats by intraperitoneal injection of 60 mg/kg streptozotocin. After 4-weeks, rats were pretreated orally with 30 mg/kg Rivaroxaban/saline; prothrombin time was monitored. IS and ET was induced after 1 h, by thread-induced transient middle cerebral artery occlusion (tMCAO) that mimicked mechanical ET for proximal MCA occlusion at 60 min. After 24 h reperfusion, infarct volumes, HT, blood-brain barrier (BBB) permeability, tight junction at peri-ischemic lesion and matrix metalloproteinase-9 (MMP-9) activity was measured. Diabetic rats seemed to exhibit increased infarct volume and HT at 24 h after ET than normal rats. Infarct volumes and functional outcomes did not differ between Rivaroxaban and diabetic control groups. A significant increase in HT volumes and BBB permeability under Rivaroxaban treatment was not detected. Compared to diabetic control group, neither the occludin expression was remarkably lower in the Rivaroxaban group nor the MMP-9 activity was higher. Together, Rivaroxaban does not increase HT after ET in diabetic rats with proximal MCA occlusion, since Rivaroxaban has fewer effects on post-ischemic BBB permeability.
format article
author Feng-Di Liu
Rong Zhao
Xiao-Yan Feng
Yan-Hui Shi
Yi-Lan Wu
Xiao-Lei Shen
Ge-Fei Li
Yi-Sheng Liu
Ying Zhao
Xin-Wei He
Jia-Wen Yin
Mei-Ting Zhuang
Bing-Qiao Zhao
Jian-Ren Liu
author_facet Feng-Di Liu
Rong Zhao
Xiao-Yan Feng
Yan-Hui Shi
Yi-Lan Wu
Xiao-Lei Shen
Ge-Fei Li
Yi-Sheng Liu
Ying Zhao
Xin-Wei He
Jia-Wen Yin
Mei-Ting Zhuang
Bing-Qiao Zhao
Jian-Ren Liu
author_sort Feng-Di Liu
title Rivaroxaban does not influence hemorrhagic transformation in a diabetes ischemic stroke and endovascular thrombectomy model
title_short Rivaroxaban does not influence hemorrhagic transformation in a diabetes ischemic stroke and endovascular thrombectomy model
title_full Rivaroxaban does not influence hemorrhagic transformation in a diabetes ischemic stroke and endovascular thrombectomy model
title_fullStr Rivaroxaban does not influence hemorrhagic transformation in a diabetes ischemic stroke and endovascular thrombectomy model
title_full_unstemmed Rivaroxaban does not influence hemorrhagic transformation in a diabetes ischemic stroke and endovascular thrombectomy model
title_sort rivaroxaban does not influence hemorrhagic transformation in a diabetes ischemic stroke and endovascular thrombectomy model
publisher Nature Portfolio
publishDate 2018
url https://doaj.org/article/e9ecc3c70b3b418989989d7058ee0d7d
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