首页> 美国卫生研究院文献>Evidence-based Complementary and Alternative Medicine : eCAM >Xingnaojing Injection Protects against Cerebral Ischemia Reperfusion Injury via PI3K/Akt-Mediated eNOS Phosphorylation
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Xingnaojing Injection Protects against Cerebral Ischemia Reperfusion Injury via PI3K/Akt-Mediated eNOS Phosphorylation

机译:醒脑静注射液可通过PI3K / Akt介导的eNOS磷酸化保护脑缺血再灌注损伤

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摘要

Xingnaojing (XNJ) injection, derived from traditional Chinese medicine formulation, has a protective effect against stroke, but the underlying mechanism is unclear, which severely limited its clinical application. This research aims to elucidate the role and mechanism of XNJ in reducing cerebral ischemic reperfusion (I/R) injury. Rats received 2 h cerebral ischemia followed by reperfusion of 24 h and were intraperitoneally given 5, 10, or 15 ml/kg XNJ 24 h before ischemia and at the onset of reperfusion, respectively. TTC staining, HE staining, and neurological score were implied to evaluate the effectiveness of XNJ. The protein expressions of PI3K/Akt and eNOS signaling were measured. Experiments were further performed in human brain microvascular endothelial cells (HBMECs) to investigate the protective mechanisms of XNJ. HBMECs were subjected to 3 h oxygen and glucose deprivation following 24 h of reoxygenation (OGD) to mimic cerebral I/R in vitro. PI3K inhibitor was added with or without the preconditioning of XNJ. Multiple methods including western blot, immunofluorescence, DAPI staining, JC-1, and flow cytometry were carried out to evaluate the effect of XNJ on HBMECs. XNJ could improve rat cerebral ischemic injury and OGD induced HBMECs apoptosis. In vivo and in vitro researches indicated that the mechanism might be relevant to the activation of PI3K/Akt/eNOS signaling.
机译:醒脑静(XNJ)注射剂源自中药制剂,对中风有保护作用,但其潜在机制尚不清楚,严重限制了其临床应用。本研究旨在阐明XNJ在减少脑缺血再灌注(I / R)损伤中的作用和机制。大鼠在缺血前和再灌注开始后分别接受2h的脑缺血和24h的再灌注,分别在24h腹膜内给予5、10或15μml/ kg XNJ。暗示着TTC染色,HE染色和神经学评分可评估XNJ的有效性。测量PI3K / Akt和eNOS信号转导的蛋白表达。在人脑微血管内皮细胞(HBMEC)中进一步进行了实验,以研究XNJ的保护机制。 HBMECs在进行24小时的复氧(OGD)后要经历3小时的氧气和葡萄糖剥夺,以在体外模拟脑I / R。在进行或不进行XNJ预处理的情况下添加PI3K抑制剂。进行了多种方法,包括蛋白质印迹,免疫荧光,DAPI染色,JC-1和流式细胞术,以评估XNJ对HBMEC的作用。 XNJ可以改善大鼠脑缺血损伤和OGD诱导的HBMECs凋亡。体内和体外研究表明该机制可能与PI3K / Akt / eNOS信号的激活有关。

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