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阐明药对丹参-川芎的化学相互作用效应及其抗缺血性中风活性评价。

Elucidating the chemical interaction effects of herb pair Danshen-Chuanxiong and its anti-ischemic stroke activities evaluation.

作者信息

Pang Han-Qing, Guo Jia-Xiu, Yang Yang, Xu Li, Wang Jian, Yang Fan, Xu Zhuo-Bing, Huang Yu-Fan, Shi Wei, Lu Xin, Ibrahim Muhi Eldeen Hussien, Hu Wei-Chen, Yan Bing-Chun, Liu Liang

机构信息

Institute of Translational Medicine, School of Medicine, Yangzhou University, Yangzhou, 225009, China; Jiangsu Key Laboratory of Integrated Traditional Chinese and Western Medicine for Prevention and Treatment of Senile Diseases, Yangzhou University, Yangzhou, 225009, China; State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources, Guangxi Normal University, Guiling, 541000, China.

Institute of Translational Medicine, School of Medicine, Yangzhou University, Yangzhou, 225009, China; Jiangsu Key Laboratory of Integrated Traditional Chinese and Western Medicine for Prevention and Treatment of Senile Diseases, Yangzhou University, Yangzhou, 225009, China.

出版信息

J Ethnopharmacol. 2024 Jan 10;318(Pt B):117058. doi: 10.1016/j.jep.2023.117058. Epub 2023 Aug 17.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Salvia miltiorrhiza Bunge (Danshen) and Ligusticum chuanxiong Hort. (Chuanxiong) is the core herb pair in traditional Chinese medicines (TCMs) formulae for treating ischemic stroke. However, the synergistic effect of Danshen-Chuanxiong against anti-ischemic stroke and its compatibility mechanism remains unclear.

AIM OF THE STUDY

This study aimed to uncover the compatibility mechanism of Danshen-Chuanxiong against ischemic stroke through chemical profiling, pharmacodynamics evaluation, network pharmacology and experimental validation.

MATERIALS AND METHODS

Ultra-high performance liquid chromatography (UHPLC) combined with quadrupole time-of-flight tandem mass spectrometry (QTOF-MS) and UHPLC connected with tandem triple quadrupole mass spectrometry (QQQ-MS) were utilized to conduct the chemical interaction analysis. Then the synergistic effects of Danshen-Chuanxiong against ischemic stroke were comprehensively evaluated by the middle cerebral artery occlusion reperfusion (MCAO/R) mice model, zebrafish ischemic stroke model and glutamic acid-induced PC12 cells injury model. Afterwards, network pharmacology and molecular docking were applied to dissect the significant active compounds and potential mechanisms. Finally, the key target proteins were experimentally validated by Western blot.

RESULTS

83 compounds were characterized in Danshen-Chuanxiong by UHPLC-QTOF-MS analysis, and 4 compounds were tentatively identified for the first time. The quantification results (24 accurately identified compounds) in 13 proportions of Danshen-Chuanxiong revealed that Danshen significantly increased the dissolution of most phthalides (from Chuanxiong), while Chuanxiong facilitated the dissolution of most phenolic acids (from Danshen) in solution. The anti-ischemic stroke effects of Danshen-Chuanxiong were significantly better than Danshen or Chuanxiong in attenuating infarct size, reducing brain edema and neurological scores in MCAO/R mice. Also, compared with single herbs, this herb pair exerted better effects of suppressing the incidence of cerebral thrombosis in zebrafish, and increasing the cell viability of glutamic acid-induced PC12 cells. In network pharmacology, 7 effective compounds (rosmarinic acid, chlorogenic acid, salvianolic acid B, (Z)-ligustilide, ferulic acid, caffeic acid, tanshinone IIA) and 5 hub targets (AKT, TNF-α, IL-1β, CASP3 and BCL2) as well as 4 key pathways were predicted. Western blot results showed that Danshen-Chuanxiong exert therapeutic effects mainly through decreasing the protein expressions of TNF-α, IL-1β and Cleaved-CASP3, elevating the levels of p-AKT and BCL2.

CONCLUSIONS

This work provided an integration strategy for uncovering the synergistic effects and compatibility mechanism of Danshen-Chuanxiong herb pair for treating ischemic stroke, and laid foundation for the further development and utilization of this herb pair.

摘要

民族药理学相关性

丹参和川芎是用于治疗缺血性中风的中药方剂中的核心药对。然而,丹参 - 川芎抗缺血性中风的协同作用及其配伍机制尚不清楚。

研究目的

本研究旨在通过化学表征、药效学评价、网络药理学和实验验证揭示丹参 - 川芎抗缺血性中风的配伍机制。

材料与方法

采用超高效液相色谱(UHPLC)结合四极杆飞行时间串联质谱(QTOF-MS)以及UHPLC连接串联三重四极杆质谱(QQQ-MS)进行化学相互作用分析。然后通过大脑中动脉闭塞再灌注(MCAO/R)小鼠模型、斑马鱼缺血性中风模型和谷氨酸诱导的PC12细胞损伤模型全面评估丹参 - 川芎对缺血性中风的协同作用。之后,应用网络药理学和分子对接来剖析重要活性成分和潜在机制。最后,通过蛋白质免疫印迹法对关键靶蛋白进行实验验证。

结果

通过UHPLC-QTOF-MS分析在丹参 - 川芎中鉴定出83种化合物,其中4种化合物为首次初步鉴定。13种比例的丹参 - 川芎定量结果(24种准确鉴定的化合物)表明,丹参显著增加了大多数苯酞类成分(来自川芎)的溶出度,而川芎促进了大多数酚酸类成分(来自丹参)在溶液中的溶出。在MCAO/R小鼠中,丹参 - 川芎的抗缺血性中风作用在减轻梗死体积、减轻脑水肿和神经功能评分方面明显优于丹参或川芎。此外,与单味药相比,该药对在抑制斑马鱼脑血栓形成发生率以及提高谷氨酸诱导的PC12细胞活力方面具有更好的效果。在网络药理学中,预测了7种有效成分(迷迭香酸、绿原酸、丹酚酸B、(Z)-藁本内酯、阿魏酸、咖啡酸、丹参酮IIA)和5个核心靶点(AKT、TNF-α、IL-1β、CASP3和BCL2)以及4条关键通路。蛋白质免疫印迹结果表明,丹参 - 川芎主要通过降低TNF-α、IL-1β和Cleaved-CASP3的蛋白表达,升高p-AKT和BCL2水平发挥治疗作用。

结论

本研究为揭示丹参 - 川芎药对治疗缺血性中风的协同作用及配伍机制提供了一种整合策略,为该中药药对的进一步开发利用奠定了基础。

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