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丹参川芎嗪注射液通过抑制 TLR2/TLR4-MyD88-NF-κB 通路减轻大脑中动脉阻塞小鼠的脑缺血再灌注损伤。

Danshen-Chuanxiongqin Injection attenuates cerebral ischemic stroke by inhibiting neuroinflammation via the TLR2/ TLR4-MyD88-NF-κB Pathway in tMCAO mice.

机构信息

Pharmaceutical Informatics Institute, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, China.

Pharmaceutical Informatics Institute, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, China.

出版信息

Chin J Nat Med. 2021 Oct;19(10):772-783. doi: 10.1016/S1875-5364(21)60083-3.

Abstract

Danshen-Chuanxiongqin Injection (DCI) is a commonly used traditional Chinese medicine for the treatment of cerebral ischemic stroke in China. However, its underlying mechanisms remain completely understood. The current study was designed to explore the protective mechanisms of DCI against cerebral ischemic stroke through integrating whole-transcriptome sequencing coupled with network pharmacology analysis. First, using a mouse model of cerebral ischemic stroke by transient middle cerebral artery occlusion (tMCAO), we found that DCI (4.10 mL·kg) significantly alleviated cerebral ischemic infarction, neurological deficits, and the pathological injury of hippocampal and cortical neurons in mice. Next, the whole-transcriptome sequencing was performed on brain tissues. The cerebral ischemia disease (CID) network was constructed by integrating transcriptome sequencing data and cerebrovascular disease-related genes. The results showed CID network was imbalanced due to tMCAO, but a recovery regulation was observed after DCI treatment. Pathway analysis of the key genes with recovery efficiency showed that the neuroinflammation signaling pathway was highly enriched, while the TLR2/TLR4-MyD88-NF-κB pathway was predicted to be affected. Consistently, the in vivo validation experiments confirmed that DCI exhibited protective effects against cerebral ischemic stroke by inhibiting neuroinflammation via the TLR2/TLR4-MyD88-NF-κB pathway. More interestingly, DCI markedly suppressed the neutrophils infiltrated into the brain parenchyma via the choroid plexus route and showed anti-neuroinflammation effects. In conclusion, our results provide dependable evidence that inhibiting neuroinflammation via the TLR2/TLR4-MyD88-NF-κB pathway is the main mechanism of DCI against cerebral ischemic stroke in mice.

摘要

丹参川芎嗪注射液(DCI)是一种常用于治疗中国缺血性脑卒中的传统中药。然而,其潜在机制尚不完全清楚。本研究旨在通过整合全转录组测序和网络药理学分析,探讨 DCI 对缺血性脑卒中的保护机制。首先,我们采用短暂性大脑中动脉闭塞(tMCAO)诱导的小鼠缺血性脑卒中模型,发现 DCI(4.10 mL·kg)可显著减轻缺血性脑梗死、神经功能缺损以及海马和皮质神经元的病理损伤。其次,我们对脑组织进行了全转录组测序。通过整合转录组测序数据和脑血管疾病相关基因,构建了脑缺血疾病(CID)网络。结果表明,tMCAO 导致 CID 网络失衡,但 DCI 治疗后观察到恢复调节。对具有恢复效率的关键基因进行通路分析表明,神经炎症信号通路显著富集,而 TLR2/TLR4-MyD88-NF-κB 通路被预测受到影响。体内验证实验结果一致表明,DCI 通过抑制 TLR2/TLR4-MyD88-NF-κB 通路的神经炎症,发挥对缺血性脑卒中的保护作用。更有趣的是,DCI 可通过脉络丛途径显著抑制中性粒细胞浸润脑实质,并发挥抗炎作用。综上所述,本研究结果为 DCI 通过 TLR2/TLR4-MyD88-NF-κB 通路抑制神经炎症防治缺血性脑卒中提供了可靠证据。

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