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结合系统药理学、代谢组学和转录组学揭示丹参-牡丹皮药对治疗缺血性中风的机制。

Combining systems pharmacology, metabolomics, and transcriptomics to reveal the mechanism of Salvia miltiorrhiza-Cortex moutan herb pair for the treatment of ischemic stroke.

作者信息

Zhao Chao, Bai Xiaodan, Ding Yi, Wen Aidong, Fu Qiang

机构信息

Department of Pharmaceutical Analysis, School of Pharmacy, Xi'an Jiaotong University, Xi'an, China.

Department of Pharmacy, Xijing Hospital, Air Force Medical University, Xi'an, China.

出版信息

Front Pharmacol. 2024 Sep 9;15:1431692. doi: 10.3389/fphar.2024.1431692. eCollection 2024.

Abstract

Ischemic stroke (IS), predominantly triggered by blockages in cerebral blood flow, is increasingly recognized as a critical public health issue. The combination of Salvia miltiorrhiza (SM) and Cortex moutan (CM), traditional herbs in Eastern medicine, are frequently used for managing heart and brain vascular conditions. However, the exact mechanisms by which this herb pair (SC) combats IS remain largely unexplored. This investigation focuses on pinpointing the active constituents in SC that contribute to its protective role and deciphering the mechanisms countering cerebral ischemia, particularly in a middle cerebral artery occlusion (MCAO) rat model. We employed UPLC-Q-TOF-MS/MS alongside network pharmacology for predicting SC's target actions against IS. Key ingredients were examined for their interaction with principal targets using molecular docking. The therapeutic impact was gauged through H&E, TUNEL, and Nissl staining, complemented by transcriptomic and metabolomic integration for mechanistic insights, with vital genes confirmed via western blot. UPLC-Q-TOF-MS/MS analysis revealed that the main components of SC included benzoylpaeoniflorin, salvianolic acid B, oxypaeoniflora, salvianolic acid A, and others. Network pharmacology analysis indicated that SC's mechanism in treating IS primarily involves inflammation, angiogenesis, and cell apoptosis-related pathways, potentially through targets such as AKT1, TNF, PTGS2, MMP9, PIK3CA, and VEGFA. Molecular docking underscored strong affinities between these constituents and their targets. Our empirical studies indicated SC's significant role in enhancing neuroprotection in IS, with transcriptomics suggesting the involvement of the VEGFA/PI3K/AKT pathway and metabolomics revealing improvements in various metabolic processes, including amino acids, glycerophospholipids, sphingomyelin, and fatty acids metabolisms.

摘要

缺血性中风(IS)主要由脑血流阻塞引发,日益被视为一个关键的公共卫生问题。丹参(SM)和牡丹皮(CM)这两种传统的东方草药常用于治疗心脏和脑血管疾病。然而,这一药对(SC)对抗IS的确切机制在很大程度上仍未得到探索。本研究聚焦于确定SC中有助于其发挥保护作用的活性成分,并解读对抗脑缺血的机制,特别是在大脑中动脉闭塞(MCAO)大鼠模型中。我们采用超高效液相色谱-四极杆飞行时间串联质谱(UPLC-Q-TOF-MS/MS)结合网络药理学来预测SC对IS的靶向作用。使用分子对接研究关键成分与主要靶点的相互作用。通过苏木精-伊红(H&E)、末端脱氧核苷酸转移酶介导的缺口末端标记(TUNEL)和尼氏染色评估治疗效果,并通过转录组学和代谢组学整合以深入了解机制,通过蛋白质免疫印迹法确认关键基因。UPLC-Q-TOF-MS/MS分析显示,SC的主要成分包括苯甲酰芍药苷、丹酚酸B、氧化芍药苷、丹酚酸A等。网络药理学分析表明,SC治疗IS的机制主要涉及炎症、血管生成和细胞凋亡相关途径,可能通过AKT1、肿瘤坏死因子(TNF)、环氧合酶-2(PTGS2)、基质金属蛋白酶-9(MMP9)、磷脂酰肌醇-3激酶催化亚基α(PIK3CA)和血管内皮生长因子A(VEGFA)等靶点。分子对接强调了这些成分与其靶点之间的强亲和力。我们的实证研究表明,SC在增强IS中的神经保护作用方面具有重要作用,转录组学表明血管内皮生长因子A/磷脂酰肌醇-3激酶/蛋白激酶B(VEGFA/PI3K/AKT)途径参与其中,代谢组学揭示了各种代谢过程的改善,包括氨基酸、甘油磷脂、鞘磷脂和脂肪酸代谢。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fb9/11417465/62bdd83b0ee7/fphar-15-1431692-g001.jpg

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