整合网络药理学和代谢组学揭示民族药 Rodgersia sambucifolia Hemsl.

IF 4.7 2区 医学 Q1 CHEMISTRY, MEDICINAL
Drug Design, Development and Therapy Pub Date : 2024-10-24 eCollection Date: 2024-01-01 DOI:10.2147/DDDT.S479341
Jiayue Zhou, Yingxiang Wu, Zhiyan Lu, Yan Wang
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引用次数: 0

摘要

目的:延胡索(Rodgersia sambucifolia Hemsl,又名延陀)是一种传统中药,其根茎是常用的药材,主要用于调节人体免疫功能。然而,对其活性成分和体内潜在作用机制的研究相对较少:首先,利用 UPLC-Q-TOF MS/MS 技术鉴定和分析了其体外化学成分。然后给大鼠腹腔注射环磷酰胺(CTX),建立免疫抑制模型。对生理和生化参数、器官指数以及组织病理学结果进行疗效评估。随后,利用多元统计分析确定了大鼠血清中的潜在生物标志物,并利用 MetaboAnalyst 和 KEGG 等在线平台进行了富集和拓扑分析,以揭示关键的代谢途径及其在免疫调节网络中的作用。最后,利用网络药理学和分子对接技术对体内和体外成分以及代谢途径进行了综合分析,以阐明它们在机体免疫中的作用机制:结果:共鉴定出28种体外化学成分,药效学实验证实了延胡索酸具有免疫调节作用,尤其是在大剂量给药组。代谢组学分析表明,在正离子和负离子模式下,共鉴定出 37 个潜在的免疫相关生物标记物,涉及精氨酸生物合成、嘧啶代谢、核黄素代谢等 16 个代谢途径。网络药理学和分子对接的结果表明,延胡索酸可能通过与免疫系统的相互作用影响 7-O-麦芽酰儿茶素、犬牙交错苷、槲皮素-7-O-beta-D-吡喃葡萄糖苷和 1.6-双-O-麦芽酰-beta-D-葡萄糖,其重要作用途径包括半乳糖代谢、糖酵解/糖元生成、嘧啶代谢和核黄素代谢:在我们的实验中,我们证实了延胡索酸对免疫功能低下大鼠的机体调节作用,阐明了其可能发挥作用的关键成分、靶蛋白和途径,并为后续研究提供了可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Integrating Network Pharmacology and Metabolomics to Reveal the Immunomodulatory Mechanism of Ethnomedicine Rodgersia sambucifolia Hemsl.

Purpose: Rodgersia sambucifolia Hemsl (also known as Yantuo ) is a traditional Chinese medicine commonly utilized as a medicinal herb with its rhizomes, mainly used to regulate the immune function of the human body. However, relatively few studies have investigated its active components and potential mechanisms of action in vivo.

Methods: First, the chemical composition in vitro was identified and analyzed using the UPLC-Q-TOF MS/MS technique. Cyclophosphamide (CTX) was then administered intraperitoneally to rats to establish an immunosuppression model. Physiological and biochemical parameters, organ indices, and histopathological findings were evaluated for efficacy. Subsequently, potential biomarkers in rat serum were identified using multivariate statistical analysis and enriched and topologized using online platforms such as MetaboAnalyst and KEGG to reveal the critical metabolic pathways and their roles in the immunomodulatory network. Finally, the integrated analysis of components in vivo and in vitro, along with metabolic pathways, was performed using network pharmacology and molecular docking technology to elucidate the mechanisms of their roles in organismal immunity.

Results: A total of 28 chemical components in vitro were identified, while pharmacodynamic experiments confirmed the immunomodulatory effects of Yantuo , especially in the high-dose administration group. Metabolomics analysis showed that 37 potential immune-related biomarkers were identified in positive and negative ion modes, involving 16 metabolic pathways such as arginine biosynthesis, pyrimidine metabolism, and riboflavin metabolism. The results of network pharmacology and molecular docking indicated that Yantuo may affect 7-O-galloyl-catechin, Cynaroside, Quercetin-7-O-beta-D-glucopyranoside, and 1.6-bis-O-galloyl-beta-D-glucose through interactions with the immune system, with significant pathways of action including galactose metabolism, glycolysis/gluconeogenesis, pyrimidine metabolism, and riboflavin metabolism.

Conclusion: In our experiments, we confirmed the organismal modulatory effect of Yantuo on immunocompromised rats, clarified the key components, target proteins, and pathways of its possible action, and provided possibilities for follow-up studies.

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来源期刊
Drug Design, Development and Therapy
Drug Design, Development and Therapy CHEMISTRY, MEDICINAL-PHARMACOLOGY & PHARMACY
CiteScore
9.00
自引率
0.00%
发文量
382
审稿时长
>12 weeks
期刊介绍: Drug Design, Development and Therapy is an international, peer-reviewed, open access journal that spans the spectrum of drug design, discovery and development through to clinical applications. The journal is characterized by the rapid reporting of high-quality original research, reviews, expert opinions, commentary and clinical studies in all therapeutic areas. Specific topics covered by the journal include: Drug target identification and validation Phenotypic screening and target deconvolution Biochemical analyses of drug targets and their pathways New methods or relevant applications in molecular/drug design and computer-aided drug discovery* Design, synthesis, and biological evaluation of novel biologically active compounds (including diagnostics or chemical probes) Structural or molecular biological studies elucidating molecular recognition processes Fragment-based drug discovery Pharmaceutical/red biotechnology Isolation, structural characterization, (bio)synthesis, bioengineering and pharmacological evaluation of natural products** Distribution, pharmacokinetics and metabolic transformations of drugs or biologically active compounds in drug development Drug delivery and formulation (design and characterization of dosage forms, release mechanisms and in vivo testing) Preclinical development studies Translational animal models Mechanisms of action and signalling pathways Toxicology Gene therapy, cell therapy and immunotherapy Personalized medicine and pharmacogenomics Clinical drug evaluation Patient safety and sustained use of medicines.
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