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Dissection of Mechanisms of a Chinese Medicinal Formula: Danhong Injection Therapy for Myocardial Ischemia/Reperfusion Injury In Vivo and In Vitro

机译:剖析中药配方的机理:丹红注射液对体内和体外心肌缺血/再灌注损伤的作用

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摘要

Traditional Chinese medicine uses a systemic treatment approach, targeting multiple etiological factors simultaneously. Danhong injection (DHI), a very popular Chinese medicine injection, is reported to be effective for many cardiovascular conditions. The primary active ingredients of DHI, and their systemic and interrelated mechanism have not been evaluated in an established myocardial ischemia/reperfusion (MI/R) model. We identified the main active constituents in DHI, including hydroxysafflor yellow A (A), salvianolic acid B (B), and danshensu (C), by HPLC fingerprint analysis and assessed their effect on MI/R rats and cardiomyocytes. These 3 compounds and DHI all decreased the levels of IL-1, TNF-α, and MDA, increased those of IL-10 and SOD activity in vivo and in vitro, and had antiapoptotic effects, as shown by flow cytometric analysis and TUNEL assay. Moreover, these compounds increased phosphorylation of Akt and ERK1/2 in cardiomyocytes. Interestingly, we found compound A exerted a more prominent anti-inflammatory effect than B and C, by decreasing NF-κB levels; compound B had more powerful antioxidative capacity than A and C, by increasing Nrf2 expression; compound C had stronger antiapoptotic ability than A and B, by lowering caspase-3 activity. Our results elucidate the mechanisms by which DHI protects against MI/R induced injury.
机译:中医采用全身性治疗方法,同时针对多种病因。丹红注射液(DHI)是一种非常受欢迎的中药注射剂,据报道对许多心血管疾病有效。在建立的心肌缺血/再灌注(MI / R)模型中,尚未评估DHI的主要活性成分及其系统性和相关机制。我们通过HPLC指纹图谱分析确定了DHI中的主要活性成分,包括羟基红花黄A(A),丹酚酸B(B)和丹参素(C),并评估了它们对MI / R大鼠和心肌细胞的作用。这三种化合物和DHI均降低了IL-1,TNF-α和MDA的水平,体内和体外均增加了IL-10和SOD的活性,并具有抗凋亡作用,如流式细胞仪和TUNEL分析所示。此外,这些化合物增加了心肌细胞中Akt和ERK1 / 2的磷酸化。有趣的是,我们发现化合物A通过降低NF-κB水平,比B和C具有更显着的抗炎作用。通过增加Nrf2表达,化合物B具有比A和C更强的抗氧化能力。化合物C通过降低caspase-3活性比A和B具有更强的抗凋亡能力。我们的结果阐明了DHI预防MI / R诱导的损伤的机制。

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