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川芎嗪通过靶向星形胶质细胞中的内皮素-1/Akt通路减轻缺血性中风对血脑屏障的损伤。

Tetramethylpyrazine attenuates the blood-brain barrier damage against ischemic stroke by targeting endothelin-1/Akt pathway in astrocytes.

作者信息

Deng Minzhen, Cai Yuefang, Wang Yu, Hu Dafeng, Li Yan, Ning Zhenqiu, Wang Chengyi, Chung Sookja Kim, Huang Yan, Sun Jingbo, Zhou Lihua, Li Jie, Cheng Xiao

机构信息

Chinese Medicine Guangdong Laboratory, State Key Laboratory of Traditional Chinese Medicine Syndrome, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.

Guangdong Provincial Key Laboratory of Research on Emergency in TCM, Guangzhou, China.

出版信息

Front Pharmacol. 2025 May 16;16:1571552. doi: 10.3389/fphar.2025.1571552. eCollection 2025.

Abstract

Our study focused on the role of traditional Chinese medicine in stroke therapy, specifically targeting endothelin-1 (ET-1) in astrocytes to alleviate ischemic brain injury. Utilizing oxygen-glucose deprivation/reoxygenation (OGD/R) and middle cerebral artery occlusion (MCAO) models, we mimicked cerebral ischemia in both cell cultures and mice. Tetramethylpyrazine (TMP), a component of the Chinese medicine, was identified as a potential therapeutic agent. It significantly increased cell viability, reduced ET-1 expression, and mitigated OGD-induced astrocyte damage, as shown by experiments with ET-1 siRNA and cell lines overexpressing ET-1. In the MCAO animal model, TMP improved neurological scores, decreased infarct size, and lowered ET-1 levels, thus strengthening the blood-brain barrier and reducing oxidative stress. TMP's neuroprotective effects were further linked to the upregulation of phosphorylated AKT (p-AKT), indicating that the AKT pathway may function downstream of ET-1. These results highlight TMP's potential in treating ischemic stroke by modulating the ET-1 and AKT signaling pathways, offering a promising avenue for future stroke therapies.

摘要

我们的研究聚焦于中药在中风治疗中的作用,特别针对星形胶质细胞中的内皮素 -1(ET-1)以减轻缺血性脑损伤。利用氧糖剥夺/复氧(OGD/R)和大脑中动脉闭塞(MCAO)模型,我们在细胞培养和小鼠中模拟了脑缺血。川芎嗪(TMP)作为中药的一种成分,被确定为一种潜在的治疗药物。实验表明,ET-1 小干扰 RNA 和过表达 ET-1 的细胞系实验显示,它能显著提高细胞活力,降低 ET-1 表达,并减轻 OGD 诱导的星形胶质细胞损伤。在 MCAO 动物模型中,TMP 改善了神经功能评分,减小了梗死面积,并降低了 ET-1 水平,从而加强了血脑屏障并减轻了氧化应激。TMP 的神经保护作用进一步与磷酸化 AKT(p-AKT)的上调相关,表明 AKT 通路可能在 ET-1 的下游发挥作用。这些结果突出了 TMP 通过调节 ET-1 和 AKT 信号通路治疗缺血性中风的潜力,为未来的中风治疗提供了一条有前景的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b66a/12122491/61f0a74a174a/fphar-16-1571552-g001.jpg

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