首页> 美国卫生研究院文献>Scientific Reports >Rhein and rhubarb similarly protect the blood-brain barrier after experimental traumatic brain injury via gp91phox subunit of NADPH oxidase/ROS/ERK/MMP-9 signaling pathway
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Rhein and rhubarb similarly protect the blood-brain barrier after experimental traumatic brain injury via gp91phox subunit of NADPH oxidase/ROS/ERK/MMP-9 signaling pathway

机译:大黄酸和大黄通过NADPH氧化酶/ ROS / ERK / MMP-9信号通路的gp91phox亚基类似地保护实验性颅脑损伤后的血脑屏障

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摘要

Oxidative stress chiefly contributes to the disruption of the BBB following traumatic brain injury (TBI). The Chinese herbal medicine rhubarb is a promising antioxidant in treating TBI. Here we performed in vivo and in vitro experiments to determine whether rhubarb and its absorbed bioactive compound protected the BBB after TBI by increasing ZO-1 expression through inhibition of gp91phox subunit of NADPH oxidase/ROS/ERK/MMP-9 pathway. Rats were subjected to the controlled cortical impact (CCI) model, and primary rat cortical astrocytes were exposed to scratch-wound model. The liquid chromatography with tandem mass spectrometry method showed that rhein was the compound absorbed in the brains of CCI rats after rhubarb administration. The wet-dry weights and Evans blue measurements revealed that rhubarb and rhein ameliorated BBB damage and brain edema in CCI rats. Western blots showed that rhubarb and rhein downregulated GFAP in vitro. RT-PCR, immunohistochemistry, Western blot and dichlorodihydrofluorescein diacetate analysis indicated that rhubarb prevented activation of gp91phox subunit of NADPH oxidase induced ROS production, subsequently inhibited ERK/MMP-9 pathway in vivo and in vitro. Interestingly, rhein and rhubarb similarly protected the BBB by inhibiting this signaling cascade. The results provide a novel herbal medicine to protect BBB following TBI via an antioxidative molecular mechanism.
机译:氧化应激主要导致脑外伤(TBI)后血脑屏障的破坏。大黄是治疗TBI的有希望的抗氧化剂。在这里我们进行了体内和体外实验,以确定大黄及其吸收的生物活性化合物是否通过抑制NADPH氧化酶/ ROS / ERK /的gp91 phox 亚基增加ZO-1表达来保护TBI后的BBB。 MMP-9途径。将大鼠置于受控皮质撞击(CCI)模型中,并将原代大鼠皮质星形胶质细胞暴露于刮伤模型中。液相色谱-串联质谱法表明,大黄给药后,大黄酸是CCI大鼠脑中吸收的化合物。干湿重和伊文思蓝测量结果表明,大黄和大黄酸改善了CCI大鼠的BBB损伤和脑水肿。蛋白质印迹显示大黄和大黄酸在体外下调了GFAP。 RT-PCR,免疫组化,Western blot和二氯二氢荧光素二乙酸酯分析表明,大黄可抑制NADPH氧化酶诱导的ROS产生的gp91 phox 亚基的活化,进而抑制体内外ERK / MMP-9途径。有趣的是,大黄酸和大黄通过抑制这种信号级联反应类似地保护了血脑屏障。结果提供了一种新颖的草药,通过抗氧化分子机制保护TBI后的BBB。

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