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

被引:17
作者
Xu Xiao-Jing [1 ]
Long Jin-Bo [1 ]
Jin Kai-Yu [1 ]
Chen Li-Bing [1 ]
Lu Xiao-Yan [1 ]
Fan Xiao-Hui [1 ,2 ]
机构
[1] Zhejiang Univ, Coll Pharmaceut Sci, Pharmaceut Informat Inst, Hangzhou 310058, Peoples R China
[2] Tianjin Univ Tradit Chinese Med, State Key Lab Component Based Chinese Med, Tianjin 301617, Peoples R China
关键词
Cerebral ischemic stroke; Network pharmacology; Neuroinflammation; Neutro-phil; Choroid plexus; Danshen-Chuanxiongqin Injection; CHOROID-PLEXUS; KAPPA-B; MEDICINE; INJURY; ISCHEMIA/REPERFUSION; INVASION; MYD88; CELLS;
D O I
10.1016/S1875-5364(21)60083-3
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
[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 center dot kg-1) 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-kappa B 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-kappa B 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-kappa B pathway is the main mechanism of DCI against cerebral ischemic stroke in mice.
引用
收藏
页码:772 / 783
页数:12
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