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黄芪甲苷对蛛网膜下腔出血实验大鼠模型迟发性脑血管痉挛的保护作用

Protective Effects of Astragaloside IV on Delayed Cerebral Vasospasm in an Experimental Rat Model of Subarachnoid Hemorrhage.

作者信息

Ma Yudong, Qiao Guangyu, Yin Yiheng, Zhang Yan, Yu Yaoyu, Yu Xinguang

机构信息

Department of Neurosurgery, Chinese PLA General Hospital, Beijing, China.

Department of Neurosurgery, the Affiliated Hospital of Logistics University of Chinese People's Armed Police Forces, Tianjin, China.

出版信息

World Neurosurg. 2018 Oct;118:e443-e448. doi: 10.1016/j.wneu.2018.06.212. Epub 2018 Jul 4.

Abstract

BACKGROUND

Delayed cerebral vasospasm is an important cause of morbidity and mortality in patients with subarachnoid hemorrhage (SAH). This study aimed to assess the effects of Astragaloside IV (AS-IV) on delayed cerebral vasospasm after SAH.

METHODS

A rat model of SAH was established by puncturing one side of the internal carotid artery. Then, rats received daily intraperitoneal injections of AS-IV (20 mg/kg; SAH-AS-IV group), 0.1% dimethyl sulfoxide (DMSO) (SAH-DMSO group), or saline (SAH group) for 5 days; an additional control group consisted of rats receiving sham surgery and saline injections. Morphologic characteristics of the basilar artery (BA) were measured from histologic sections stained with hematoxylin and eosin and used as indicators of cerebral vasospasm. Immunohistochemistry was used to detect Toll-like receptor-4 (TLR4) and nuclear factor kappa B (NF-κB) p65 protein levels in the BA. Enzyme-linked immunosorbent assay was used to measure the plasma concentrations of tumor necrosis factor-alpha and interleukin-6.

RESULTS

Compared with controls, the SAH-DMSO and SAH groups showed increased wall thickness and reduced luminal cross-sectional area (indicative of vasospasm) and increased TLR4 expression and enhanced NF-κB activation in the BA, as well as elevated plasma levels of tumor necrosis factor-alpha and interleukin-6. Administration of AS-IV was associated with significant attenuation of all the aforementioned changes induced by SAH (P < 0.05).

CONCLUSIONS

AS-IV may attenuate delayed cerebral vasospasm after SAH through inhibition of TLR4/NF-κB-mediated inflammatory signaling pathways.

摘要

背景

迟发性脑血管痉挛是蛛网膜下腔出血(SAH)患者发病和死亡的重要原因。本研究旨在评估黄芪甲苷IV(AS-IV)对SAH后迟发性脑血管痉挛的影响。

方法

通过穿刺一侧颈内动脉建立SAH大鼠模型。然后,大鼠连续5天每天腹腔注射AS-IV(20mg/kg;SAH-AS-IV组)、0.1%二甲基亚砜(DMSO)(SAH-DMSO组)或生理盐水(SAH组);另一个对照组由接受假手术和生理盐水注射的大鼠组成。从苏木精和伊红染色的组织切片测量基底动脉(BA)的形态学特征,并将其用作脑血管痉挛的指标。采用免疫组织化学法检测BA中Toll样受体4(TLR4)和核因子κB(NF-κB)p65蛋白水平。采用酶联免疫吸附测定法测量血浆中肿瘤坏死因子-α和白细胞介素-6的浓度。

结果

与对照组相比,SAH-DMSO组和SAH组BA的壁厚增加、管腔横截面积减小(提示血管痉挛),TLR4表达增加、NF-κB激活增强,血浆中肿瘤坏死因子-α和白细胞介素-6水平升高。AS-IV给药可显著减轻SAH引起的上述所有变化(P<0.05)。

结论

AS-IV可能通过抑制TLR4/NF-κB介导的炎症信号通路减轻SAH后的迟发性脑血管痉挛。

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