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A hemorrhagic transformation model of mechanical stroke therapy with acute hyperglycemia in mice

机译:小鼠急性高血糖治疗机械卒中治疗的出血性转化模型

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Abstract Clinical benefit for mechanical thrombectomy (MT) in stroke was recently demonstrated in multiple large prospective studies. Acute hyperglycemia (HG) is an important risk factor of poor outcome in stroke patients, including those that underwent MT. The aim of this therapy is to achieve a complete reperfusion in a short time, given that reperfusion damage is dependent on the duration of ischemia. Here, we investigated the effects of acute HG in a mouse model of ischemic stroke induced by middle cerebral artery occlusion (MCAO). Hyperglycemic (intraperitoneal [ip] injection of glucose) and control (ip saline injection) 10‐week male C57BL6 mice were subjected to MCAO (30, 90, and 180 min) followed by reperfusion obtained by withdrawal of the monofilament. Infarct volume, hemorrhagic transformation (HT), neutrophil infiltration, and neurological scores were assessed at 24 hr by performing vital staining, ELISA immunofluorescence, and behavioral test, respectively. Glucose injection led to transient HG (blood glucose?=?250–390 mg/dL) that significantly increased infarct volume, HT, and worsened neurological outcome. In addition, we report that HG promoted blood‐brain barrier disruption as shown by hemoglobin accumulation in the brain parenchyma and tended to increase neutrophil extravasation within the infarcted area. Acute HG increased neurovascular damage for all MCAO durations tested. HTs were observed as early as 90 min after ischemia under hyperglycemic conditions. This model mimics MT ischemia/reperfusion and allows the exploration of brain injury in hyperglycemic conditions.
机译:摘要在多次大型前瞻性研究中,最近展示了卒中机械血栓切除术(MT)的临床效益。急性高血糖(Hg)是中风患者差异差的重要危险因素,包括接受MT的人。这种治疗的目的是在短时间内实现完全再灌注,因为再灌注损伤取决于缺血的持续时间。在这里,我们研究了急性Hg在中脑动脉闭塞(MCAO)诱导的缺血性卒中小鼠模型中的影响。高血糖(腹膜内[IP]注射葡萄糖)和对照(IP盐水注射)10周雄性C57BL6小鼠进行MCAO(30,90和180分钟),然后通过撤离单丝获得的再灌注。通过进行生命染色,ELISA免疫荧光和行为试验,在24小时评估Imarct体积,出血性转化(HT),中性粒细胞浸润和神经学评分。葡萄糖注射导致瞬时Hg(血糖?=Δ= 250-390mg / dl),显着增加了梗塞体积,HT和恶化的神经结果。此外,我们报告称HG促进了脑医学中血红蛋白积累所示的血脑屏障破坏,并倾向于增加梗死区域内的中性粒细胞外渗。急性Hg对测试的所有MCAO持续时间增加了神经血管损伤。在高血糖条件下缺血后90分钟观察HTS。该模型模拟MT缺血/再灌注,并探讨了高血糖条件下的脑损伤。

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