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基于整合网络药理学和代谢组学的辛杏甘姜药对温肺化痰治疗慢性阻塞性肺疾病的作用。

Protective effect of Xixin-Ganjiang herb pair for warming the lungs to dissolve phlegm in chronic obstructive pulmonary disease rats based on integrated network pharmacology and metabolomics.

机构信息

Department of Rehabilitation Medicine, General Hospital of Central Theater Command, Wuhan, China.

College of Basic Medicine, Hubei University of Chinese Medicine, Wuhan, China.

出版信息

Biomed Chromatogr. 2024 Jun;38(6):e5851. doi: 10.1002/bmc.5851. Epub 2024 Mar 6.

Abstract

Xixin-Ganjiang herb pair (XGHP) is a classic combination for warming the lungs to dissolve phlegm and is often used to treat a variety of chronic lung diseases; it can treat the syndrome of cold phlegm obstruction of lungs. First, ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) was used to examine the composition of XGHP, and network pharmacology was used to predict its potential core targets and signaling pathways in the current study. Second, a rat model of chronic obstructive pulmonary disease (COPD) was established for assessing the anti-COPD activity of XGHP, and metabolomics was used to explore the biomarkers and metabolic pathways. Finally, the sample was validated using molecular docking and Western blotting. The integration of metabolomics and network pharmacology results identified 11 targets, 3 biomarkers, 3 pathways, and 2 metabolic pathways. Western blotting showed that XGHP effectively regulated the expression of core proteins via multiple signaling pathways (downregulation of toll-like receptor 4 [TLR4] and upregulation of serine/threonine-protein kinase 1 [p-AKT1] and nitric oxide synthase 3 [NOS3]). Molecular docking results showed that the 10 potentially active components of XGHP have good affinity with tumor necrosis factor-alpha (TNF-α), interleukin-6 (IL-6), matrix metalloproteinase 9 (MMP-9), TLR4, p-AKT1, and NOS3. Our findings suggest that XGHP may regulate glucolipid metabolism, improve energy supply, and inhibit inflammatory responses (TNF-α, IL-6, and MMP-9) via the PI3K-Akt signaling pathway and HIF-1 signaling pathway in the management of COPD.

摘要

心心-赣江药对(XGHP)是一种经典的温肺化痰组合,常用于治疗多种慢性肺部疾病;它可以治疗寒痰阻肺证。首先,采用超高效液相色谱-串联质谱法(UPLC-MS/MS)检测 XGHP 的组成,采用网络药理学预测其在当前研究中的潜在核心靶点和信号通路。其次,建立慢性阻塞性肺疾病(COPD)大鼠模型,评估 XGHP 的抗 COPD 活性,并采用代谢组学方法探讨生物标志物和代谢途径。最后,采用分子对接和 Western blot 对样本进行验证。代谢组学和网络药理学结果的整合确定了 11 个靶标、3 个生物标志物、3 个途径和 2 个代谢途径。Western blot 结果表明,XGHP 通过多条信号通路(下调 Toll 样受体 4 [TLR4],上调丝氨酸/苏氨酸蛋白激酶 1 [p-AKT1]和一氧化氮合酶 3 [NOS3])有效调节核心蛋白的表达。分子对接结果表明,XGHP 的 10 个潜在活性成分与肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)、基质金属蛋白酶 9(MMP-9)、TLR4、p-AKT1 和 NOS3 具有良好的亲和力。我们的研究结果表明,XGHP 可能通过 PI3K-Akt 信号通路和 HIF-1 信号通路调节糖脂代谢,改善能量供应,抑制炎症反应(TNF-α、IL-6 和 MMP-9),从而在 COPD 的治疗中发挥作用。

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