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灯盏花乙素通过抗炎和抗氧化作用缓解短暂性脑缺血/再灌注诱导的大鼠认知功能障碍。

Breviscapine Alleviates Cognitive Impairments Induced by Transient Cerebral Ischemia/Reperfusion through Its Anti-Inflammatory and Anti-Oxidant Properties in a Rat Model.

机构信息

Hangzhou Women's Hospital, No. 369 Kunpeng Road, Hangzhou 310008, Zhejiang, China.

出版信息

ACS Chem Neurosci. 2020 Dec 16;11(24):4489-4498. doi: 10.1021/acschemneuro.0c00697. Epub 2020 Dec 3.

Abstract

Cerebral ischemia/reperfusion (I/R)-induced injury is a common phenomenon of stroke, and the effective treatment for I/R-induced brain tissue damage is limited. Breviscapine has been widely used in China as herbal medicine to treat cardiovascular diseases for hundreds of years and has been demonstrated to possess potent cardiovascular pharmacological effects. This study aims to investigate the neuroprotective effect of breviscapine on cerebral I/R-induced injury. The rat model of middle cerebral artery occlusion (MCAO) was applied in our study. The cerebral I/R rats received multiple injections of breviscapine. All rats were subject to neurological behavior tests by open field test and Morris water maze test. The pro-inflammatory cytokines and oxidative stress marker levels were determined by ELISA and colorimetric analysis, respectively. We demonstrated that administration of breviscapine dose-dependently ameliorated cerebral I/R-induced injury and improved the neurological performance of cerebral I/R rats. Further studies illustrated that breviscapine treatment effectively attenuated inflammatory cytokine expression, reduced oxidative stress, and pro-apoptosis protein expression and inhibited the activation of NF-κB signaling and microglia in the I/R injury tissues. Breviscapine may serve as a single drug or a promising adjuvant that can be used in conjunction with other medicine for the treatment of cerebral I/R-induced injury.

摘要

脑缺血/再灌注(I/R)损伤是中风的一种常见现象,而针对 I/R 引起的脑组织损伤的有效治疗方法十分有限。灯盏花素作为一种草药,在中国被广泛用于治疗心血管疾病已有数百年的历史,并且已被证明具有有效的心血管药理学作用。本研究旨在探讨灯盏花素对脑 I/R 损伤的神经保护作用。我们的研究应用了大脑中动脉闭塞(MCAO)大鼠模型。脑 I/R 大鼠接受多次灯盏花素注射。所有大鼠均通过旷场试验和 Morris 水迷宫试验进行神经行为学测试。通过 ELISA 和比色分析分别测定促炎细胞因子和氧化应激标志物的水平。结果表明,灯盏花素给药可剂量依赖性地改善脑 I/R 诱导的损伤,并改善脑 I/R 大鼠的神经功能。进一步的研究表明,灯盏花素治疗可有效减轻炎症细胞因子的表达,降低氧化应激和促凋亡蛋白的表达,并抑制 I/R 损伤组织中 NF-κB 信号和小胶质细胞的激活。灯盏花素可能作为一种单一药物或一种有前途的佐剂,可与其他药物联合用于治疗脑 I/R 诱导的损伤。

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