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首页> 外文期刊>Neural regeneration research >2-(2-Benzofuranyl)-2-imidazoline treatment within 5 hours after cerebral ischemia/reperfusion protects the brain
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2-(2-Benzofuranyl)-2-imidazoline treatment within 5 hours after cerebral ischemia/reperfusion protects the brain

机译:脑缺血/再灌注后5小时内可进行2-(2-苯并呋喃基)-2-咪唑啉的治疗以保护大脑

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摘要

We previously demonstrated that administering 2-(2-benzofuranyl)-2-imidazolin (2-BFI), an imidazoline I2 receptor agonist, immediately after ischemia onset can protect the brain from ischemic insult. However, immediate administration after stroke is difficult to realize in the clinic. Thus, the therapeutic time window of 2-BFI should be determined. Sprague-Dawley rats provided by Wenzhou Medical University in China received right middle cerebral artery occlusion for 120 minutes, and were treated with 2-BFI (3 mg/kg) through the caudal vein at 0, 1, 3, 5, 7, and 9 hours after reperfusion. Neurological function was assessed using the Longa's method. Infarct volume was measured by 2,3,5-triphenyltetrazolium chloride assay. Morphological changes in the cortical penumbra were observed by hematoxylin-eosin staining under transmission electron microscopy . The apoptosis levels in the ipsilateral cortex were examined with terminal deoxynucleotidyl transferase-mediated dUTP nick end-labeling (TUNEL) assay. The protein expression of Bcl-2 and BAX was detected using immunohistochemistry. We found the following: Treatment with 2-BFI within 5 hours after reperfusion obviously improved neurological function. Administering 2-BFI within 9 hours after ischemia/reperfusion decreased infarct volume and alleviated apoptosis. 2-BFI administration at different time points after reperfusion alleviated the pathological damage of the ischemic penumbra and reduced the number of apoptotic neurons, but the protective effect was more obvious when administered within 5 hours. Administration of 2-BFI within 5 hours after reperfusion remarkably increased Bcl-2 expression and decreased BAX expression. To conclude, 2-BFI shows potent neuroprotective effects when administered within 5 hours after reperfusion, seemingly by up-regulating Bcl-2 and down-regulating BAX expression. The time window provided clinical potential for ischemic stroke by 2-BFI.
机译:我们以前证明,缺血发作后立即服用2-(2-苯并呋喃基)-2-咪唑啉(2-BFI),一种咪唑啉I2受体激动剂可以保护大脑免受缺血性损伤。但是,在临床上很难实现中风后立即给药。因此,应该确定2-BFI的治疗时间窗。由中国温州医科大学提供的Sprague-Dawley大鼠在右脑中动脉闭塞120分钟,并在尾静脉分别于0、1、3、5、7和7接受2-BFI(3 mg / kg)处理。再灌注后9小时。使用Longa方法评估神经功能。通过2,3,5-三苯基四唑鎓氯化物测定法测量梗塞体积。在透射电镜下通过苏木精-伊红染色观察到皮层半影的形态变化。用末端脱氧核苷酸转移酶介导的dUTP缺口末端标记(TUNEL)测定法检查同侧皮质中的细胞凋亡水平。使用免疫组织化学检测Bcl-2和BAX的蛋白表达。我们发现以下内容:再灌注后5小时内用2-BFI治疗明显改善了神经功能。缺血/再灌注后9小时内使用2-BFI可以减少梗塞体积并减轻细胞凋亡。在再灌注后的不同时间点进行2-BFI给药可减轻缺血性半影​​的病理损伤,并减少凋亡神经元的数量,但在5小时内给予更明显的保护作用。再灌注后5小时内施用2-BFI显着增加Bcl-2表达并降低BAX表达。总而言之,2-BFI在再灌注后5小时内给药时显示出有效的神经保护作用,似乎是通过上调Bcl-2和下调BAX表达来实现的。时间窗为2-BFI提供了缺血性卒中的临床潜力。

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