Integrated serum pharmacochemistry, network pharmacology and experimental verification to explore the mechanism of Aconiti Lateralis Radix Praeparata in treatment of lung cancer

IF 3.1 3区 医学 Q2 CHEMISTRY, ANALYTICAL
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引用次数: 0

Abstract

Aconiti Lateralis Radix Praeparata (Fuzi) is a traditional Chinese medicine (TCM) widely used in treating cancer. Our formerly investigations confirmed the anti-lung cancer efficacy of Fuzi, but systematic analysis of the ingredients of Fuzi absorbed into serum and the corresponding molecular mechanism in treating lung cancer remained unknown. In this work, UPLC-Q-TOF-MS was applied to detect the ingredients of Fuzi in rat serum. Next, the possible targets and key pathways of the components absorbed into serum of Fuzi were predicted by network pharmacology. Then, the binding activity of components and potential targets were performed by molecular docking. Afterwards, the proliferation, mitochondrial membrane potential (MMP), apoptosis and reactive oxygen species (ROS) of lung cancer cells after treatment with Fuzi-containing serum were determined by MTT assay, JC-1 fluorescent probe, Annexin V-FITC/PI double staining and DCFH-DA respectively. Finally, the predicted target was further validated with qRT-PCR. In total, identification of 20 components of Fuzi derived from rat serum were achieved. The prediction of network pharmacology indicated that these compounds might exert their therapeutic effects by modulating mTOR. The findings from molecular docking proved that fuziline, songorine, napelline and hypaconitine exhibited binding potential with the mTOR. Cancer cell experiments revealed that the Fuzi-containing serum inhibited cell proliferation, induced apoptosis, reduced MMP and increased ROS. Additionally, Fuzi-containing serum significantly reduced the mRNA expression of mTOR. This study revealed that fuziline, songorine, napelline and hypaconitine were the main ingredients of Fuzi absorbed into serum. Furthermore, Fuzi-containing serum demonstrated inhibitory effects on the proliferation of lung cancer cells and induced the apoptosis. Combined with the results of network pharmacology, molecular docking and biological verification, Fuzi-containing serum might exert its anti-lung cancer effect by inhibiting mTOR. This study would provide a deeper understanding of Fuzi in treating lung cancer and offer a scientific reference for its clinical utilization.

综合血清药理、网络药理学和实验验证,探索附子治疗肺癌的机制
附子是一种广泛用于治疗癌症的传统中药。我们以前的研究证实了附子的抗肺癌功效,但系统分析附子吸收到血清中的成分以及相应的治疗肺癌的分子机制仍然是未知的。本研究采用UPLC-Q-TOF-MS方法检测大鼠血清中的夫子成分。接着,通过网络药理学预测了夫子吸收到血清中的成分的可能靶点和关键途径。然后,通过分子对接分析了福芝成分与潜在靶点的结合活性。然后,通过MTT法、JC-1荧光探针法、Annexin V-FITC/PI双染法和DCFH-DA法分别测定了肺癌细胞在使用含夫子的血清后的增殖、线粒体膜电位(MMP)、凋亡和活性氧(ROS)情况。最后,通过 qRT-PCR 进一步验证了预测的靶点。最后,通过 qRT-PCR 进一步验证了预测的靶点,共鉴定出 20 种来自大鼠血清的夫子成分。网络药理学预测表明,这些化合物可能通过调节 mTOR 发挥治疗作用。分子对接结果证明,夫齐林、松果菊碱、萘佩林和次乌头碱具有与 mTOR 结合的潜力。癌细胞实验表明,含夫子碱的血清可抑制细胞增殖、诱导细胞凋亡、降低 MMP 和增加 ROS。此外,含福齐的血清还能显著降低 mTOR 的 mRNA 表达。这项研究表明,吸收到血清中的夫子碱、松果体碱、萘佩林和次乌头碱是夫子的主要成分。此外,含夫子的血清还具有抑制肺癌细胞增殖和诱导细胞凋亡的作用。结合网络药理学、分子对接和生物学验证结果,含夫子血清可能通过抑制 mTOR 发挥抗肺癌作用。这项研究将加深人们对夫子治疗肺癌的认识,为夫子的临床应用提供科学参考。
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来源期刊
CiteScore
6.70
自引率
5.90%
发文量
588
审稿时长
37 days
期刊介绍: This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome. Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.
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