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定量蛋白质组学和模拟对接推荐的灯盏细辛注射液对大脑中动脉闭塞大鼠的新型潜在神经保护靶点

Novel potential neuroprotective targets for DengZhanXiXin injection in middle cerebral artery occlusion rats recommended by quantitative proteomics and simulated docking.

作者信息

Li Min, Wang Linshuang, An Haiting, Li Xin, Chen Yaojing, Wei Dongfeng, Zhang Zhanjun

机构信息

State Key Laboratory of Cognitive Neuroscience and Learning and IDG/McGovern Institute for Brain Research, Beijing Normal University, Beijing, China.

BABRI Centre, Beijing Normal University, Beijing, China.

出版信息

Front Neurosci. 2025 Jul 7;19:1499214. doi: 10.3389/fnins.2025.1499214. eCollection 2025.

Abstract

Stroke, which leads to death and disability in high proportions globally, is one of the most deleterious neurological diseases. Ischemic stroke (IS) is the major cause of disease attack and accounts for ~70% of all incident stroke cases in China. Up to now, only two therapies for IS were officially approved, which are intravenous administration of recombinant tissue-plasminogen activator (rt-PA) and endovascular mechanical thrombectomy to rapidly recanalize the occluded artery, which both recanalize the occluded artery rapidly to reduce disability, but are limited in a fixed time window. In this study, the therapeutic effect of a traditional Chinese medicine, DengZhanXiXin injection (DZXI), was evaluated on middle cerebral artery occlusion (MCAO) rats at the neurobehavioral and pathophysiological levels through neurological tests, neurohistological staining, proteomic assay, and biological information analysis. We found that DZXI significantly ameliorated the neurological deficit, prevented infarct volume evolution, and protected cortical neural cells from death in ischemia penumbra on MCAO rats. Furthermore, corresponding therapeutic molecular targets were investigated through proteomic analysis of ischemic hemispheres of MCAO rats. One hundred ninety-one differentially expressed proteins involved in response to metal ions, neurofilament bundle assembly, and modulation of chemical synaptic transmission were identified between the MCAO model and DZXI groups after 7 days. DZXI influenced the expression levels of proteins in 13 specific biological functions, with cell signaling and chemical synaptic transmission-associated proteins being most affected. Subsequent molecular docking analysis predicted binding potential between key target proteins and DZXI compounds. The results suggested that DZXI ameliorates neurological deficits by potentially affecting cellular signaling and chemical synaptic transmission physiological processes.

摘要

中风在全球范围内导致高比例的死亡和残疾,是最具危害性的神经疾病之一。缺血性中风(IS)是疾病发作的主要原因,在中国约占所有新发中风病例的70%。到目前为止,IS仅有两种疗法被正式批准,即静脉注射重组组织型纤溶酶原激活剂(rt-PA)和血管内机械取栓术,以迅速使闭塞的动脉再通,这两种方法都能迅速使闭塞的动脉再通以减少残疾,但都受限于固定的时间窗。在本研究中,通过神经学测试、神经组织学染色、蛋白质组学分析和生物信息分析,在神经行为和病理生理水平上评估了一种中药灯盏细辛注射液(DZXI)对大脑中动脉闭塞(MCAO)大鼠的治疗效果。我们发现,DZXI显著改善了MCAO大鼠的神经功能缺损,防止了梗死体积扩大,并保护了缺血半暗带中的皮质神经细胞免于死亡。此外,通过对MCAO大鼠缺血半球的蛋白质组分析,研究了相应的治疗分子靶点。7天后,在MCAO模型组和DZXI组之间鉴定出191种差异表达蛋白,这些蛋白参与对金属离子的反应、神经丝束组装和化学突触传递的调节。DZXI影响了13种特定生物学功能中蛋白质的表达水平,其中细胞信号和化学突触传递相关蛋白受影响最大。随后的分子对接分析预测了关键靶蛋白与DZXI化合物之间的结合潜力。结果表明,DZXI可能通过影响细胞信号和化学突触传递生理过程来改善神经功能缺损。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e732/12277316/b828af6341d8/fnins-19-1499214-g0001.jpg

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