[Mechanism of Xuanbai Chengqi Decoction in treating acute lung injury based on network pharmacology and experimental verification].

Q3 Pharmacology, Toxicology and Pharmaceutics
Cheng Luo, Yuan-Hang Ye, Cheng Jiang, Bo Ning, Jia Ke, Gang Chen
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引用次数: 0

Abstract

This study aims to investigate the mechanism of Xuanbai Chengqi Decoction in treating acute lung injury(ALI) based on network pharmacology and animal experiments. The potential targets and signaling pathways of Xuanbai Chengqi Decoction in regulating ALI were predicted by network pharmacology. The rat model of ALI was constructed and administrated with different doses of Xuanbai Chengqi Decoction. The pathological changes in the lung tissue of rats were observed by hematoxylin-eosin(HE) staining. The levels of interleukin-6(IL-6), interleukin-1β(IL-1β), and tumor necrosis factor-α(TNF-α) in the peripheral blood were measured by enzyme-linked immunosorbent assay(ELISA). The mRNA and protein levels of factors in the phosphatidylinositol 3-kinase(PI3K)/protein kinase B(Akt)/mammalian target of rapamycin(mTOR) signaling pathway were determined by quantitative real-time PCR(qPCR) and Western blot, respectively. A total of 52 compounds from Xuanbai Chengqi Decoction were predicted to be involved in the treatment of ALI, including β-sitosterol, emodin, stigmasterol, glabridin, and aloe-emodin, which corresponded to 112 targets,and 4 723 targets of ALI were predicted. The compounds and ALI shared 94 common targets. The key targets included TNF, IL-1β,prostaglandin-endoperoxide synthase 2(PTGS2), and tumor protein 53(TP53). Lipids and atherosclerosis, p53 signaling pathway,IL-17 signaling pathway, and PI3K/Akt signaling pathway were mainly involved in the treatment. Animal experiments showed that compared with the model group, Xuanbai Chengqi Decoction alleviated the pathological changes in the lung tissue, lowered the serum levels of IL-6, IL-1β, and TNF-α, down-regulated the mRNA and protein levels of PI3K, Akt, and mTOR, and reduced the p-PI3K/PI3K, p-Akt/Akt, and p-mTOR/mTOR ratios in ALI rats. The results showed that Xuanbai Chengqi Decoction exerted its therapeutic effects on ALI via multiple components, targets, and pathways. Meanwhile, Xuanbai Chengqi Decoction may reduce the inflammation and attenuate the lung injuries of ALI rats by inhibiting the PI3K/Akt/mTOR signaling pathway.

[基于网络药理学和实验验证的玄白承气汤治疗急性肺损伤的机理]。
本研究以网络药理学和动物实验为基础,探讨宣白城芪煎膏治疗急性肺损伤(ALI)的机制。通过网络药理学预测玄白承气汤调控急性肺损伤的潜在靶点和信号通路。建立大鼠ALI模型,并给予不同剂量的宣白承气煎剂。通过苏木精-伊红(HE)染色观察大鼠肺组织的病理变化。用酶联免疫吸附法(ELISA)检测大鼠外周血中白细胞介素-6(IL-6)、白细胞介素-1β(IL-1β)和肿瘤坏死因子-α(TNF-α)的水平。实时定量 PCR(qPCR)和 Western 印迹法分别测定了磷脂酰肌醇 3-激酶(PI3K)/蛋白激酶 B(Akt)/哺乳动物雷帕霉素靶标(mTOR)信号通路因子的 mRNA 和蛋白水平。结果表明,宣白城芪煎膏中的β-谷甾醇、大黄素、豆甾醇、苁蓉苷、芦荟大黄素等52个化合物参与了ALI的治疗,对应112个靶点,预测了ALI的4 723个靶点。这些化合物和 ALI 有 94 个共同靶点。主要靶点包括 TNF、IL-1β、前列腺素内过氧化物合成酶 2(PTGS2)和肿瘤蛋白 53(TP53)。血脂和动脉粥样硬化、p53 信号通路、IL-17 信号通路和 PI3K/Akt 信号通路是治疗的主要靶点。动物实验表明,与模型组相比,宣白城芪煎膏减轻了ALI大鼠肺组织的病理变化,降低了血清中IL-6、IL-1β和TNF-α的水平,下调了PI3K、Akt和mTOR的mRNA和蛋白水平,降低了p-PI3K/PI3K、p-Akt/Akt和p-mTOR/mTOR的比值。结果表明,宣白承气汤通过多成分、多靶点、多途径对ALI发挥治疗作用。同时,宣白承气汤可通过抑制PI3K/Akt/mTOR信号通路,减轻ALI大鼠的炎症反应和肺损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Zhongguo Zhongyao Zazhi
Zhongguo Zhongyao Zazhi Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.50
自引率
0.00%
发文量
581
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