Study on the anti-atherosclerosis mechanisms of Tanyu Tongzhi formula based on network pharmacology, Mendelian randomization, and experimental verification.

IF 3.9 3区 医学 Q1 MEDICAL LABORATORY TECHNOLOGY
Pharmaceutical Biology Pub Date : 2024-12-01 Epub Date: 2024-10-25 DOI:10.1080/13880209.2024.2415666
Jin Dai, Xinbin Zhou, Xiaoming Xu, Yuangang Qiu, Shenjie Chen, Wei Mao
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引用次数: 0

Abstract

Context: Tanyu Tongzhi Formula (TTF) exhibits potential against atherosclerosis; however, its mechanisms remain unclear.

Objective: This study explores the pharmacological mechanisms of TTF in treating atherosclerosis.

Materials and methods: Network pharmacology, molecular docking, mendelian randomization (MR), and liquid chromatography-mass spectrometry (LC-MS) analyses were utilized to reveal potential targets and compounds of TTF against atherosclerosis. After exploring the appropriate concentration of TTF to treat HCAECs using Cell Counting Kit-8 (CCK-8), the HCAECs were divided into three groups: control, oxidized low-density lipoprotein (ox-LDL, 50 μg/mL), and ox-LDL (50 μg/mL) + TTF (1 mg/mL). After 24-h incubation, the efficacy of TTF was verified by CCK-8, Oil red O staining, and ELISA. The expression of key targets was detected by real-time polymerase chain reaction (qPCR) and western blotting.

Results: A total of 137 active compounds and 127 potential TTF targets against atherosclerosis were identified. MR identified ALB, TNF, PPARα, and PPARγ as key targets. Molecular docking indicated that baicalin, naringenin, and curcumin exhibited suitable binding activities to these targets, further confirming by LC-MS analysis. The IC50 of TTF in HCAECs was 18.25 mg/mL. TTF treatment significantly improved atherosclerosis by enhancing cell viability, reducing lipid accumulation, and inhibiting inflammation factors (IL6, IL1B and TNF-α) in ox-LDL-treated HCAECs. Moreover, qPCR or western blotting indicated that TTF could up-regulate PPARα and PPARγ while down-regulate TNF expression.

Discussion and conclusions: Our results revealed active compounds, key pathways, and core targets of TTF against atherosclerosis, providing experimental support for its application in treating of atherosclerosis.

基于网络药理学、孟德尔随机化和实验验证的丹俞通脉方抗动脉粥样硬化机制研究
背景:田雨通脉方(TTF)具有抗动脉粥样硬化的作用,但其作用机制尚不清楚:本研究探讨了 TTF 治疗动脉粥样硬化的药理机制:利用网络药理学、分子对接、泯灭随机化(MR)和液相色谱-质谱(LC-MS)分析揭示了 TTF 治疗动脉粥样硬化的潜在靶点和化合物。在利用细胞计数试剂盒-8(CCK-8)探索了处理HCAEC的TTF的适当浓度后,HCAEC被分为三组:对照组、氧化低密度脂蛋白(ox-LDL,50 μg/mL)组和ox-LDL(50 μg/mL)+TTF(1 mg/mL)组。孵育 24 小时后,通过 CCK-8、油红 O 染色和酶联免疫吸附试验验证 TTF 的功效。通过实时聚合酶链式反应(qPCR)和免疫印迹法检测关键靶标的表达:结果:共鉴定出 137 种活性化合物和 127 个潜在的 TTF 靶点,这些化合物和靶点都能对抗动脉粥样硬化。MR确定ALB、TNF、PPARα和PPARγ为关键靶点。分子对接表明,黄芩苷、柚皮苷和姜黄素与这些靶标具有合适的结合活性,LC-MS分析进一步证实了这一点。TTF 在 HCAECs 中的 IC50 值为 18.25 mg/mL。TTF通过提高细胞活力、减少脂质积累和抑制炎症因子(IL6、IL1B和TNF-α),明显改善了经ox-LDL处理的HCAECs的动脉粥样硬化。此外,qPCR或Western印迹表明,TTF能上调PPARα和PPARγ,同时下调TNF的表达:我们的研究结果揭示了TTF抗动脉粥样硬化的活性化合物、关键通路和核心靶点,为其在动脉粥样硬化治疗中的应用提供了实验支持。
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
Pharmaceutical Biology
Pharmaceutical Biology 医学-药学
CiteScore
6.70
自引率
2.60%
发文量
191
审稿时长
1 months
期刊介绍: Pharmaceutical Biology will publish manuscripts describing the discovery, methods for discovery, description, analysis characterization, and production/isolation (including sources and surveys) of biologically-active chemicals or other substances, drugs, pharmaceutical products, or preparations utilized in systems of traditional medicine. Topics may generally encompass any facet of natural product research related to pharmaceutical biology. Papers dealing with agents or topics related to natural product drugs are also appropriate (e.g., semi-synthetic derivatives). Manuscripts will be published as reviews, perspectives, regular research articles, and short communications. The primary criteria for acceptance and publication are scientific rigor and potential to advance the field.
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