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Quail egg yolk oil attenuates insulin resistance and redox imbalance in a high-sugar-diet drosophila model 鹌鹑蛋黄油减轻高糖饮食果蝇模型中的胰岛素抵抗和氧化还原失衡
Pub Date : 2026-03-01 Epub Date: 2025-12-06 DOI: 10.1016/j.prmcm.2025.100740
Muhammad Sani Ismaila , Ismail Sulaiman , Abdulbariu Ogirima Uhuami , Venkatesan Sundaram , Mustapha Umar Imam

Introduction

Type 2 diabetes mellitus (T2DM) is increasing globally, creating a need for natural and functional food–based therapeutic interventions. Quail egg yolk oil (QEYO), traditionally used in Chinese medicine as 鹌鹑蛋黄油 (ānchún dànhuáng yóu) for nourishing Yin and supporting metabolic balance, contains bioactive lipids and antioxidants with potential relevance for glycemic and redox regulation. This study investigated the antidiabetic and antioxidant effects of QEYO in a high-sugar diet (HSD)–induced metabolic dysfunction model in Drosophila melanogaster.

Methods

Adult male Drosophila melanogaster were fed a high-sugar diet (30% sucrose) to induce metabolic dysfunction and allocated into five groups: control, HSD, QEYO (62.5 or 125 mg/10 mL diet), and metformin (16 mg/10 mL). After 14 days of HSD induction followed by 7 days of treatment, physiological parameters, glucose and lipid biomarkers, oxidative stress indicators, and expression of key metabolic genes were assessed using enzymatic assays and RT-qPCR.

Results

HSD-fed flies developed obesity, hyperglycemia, elevated triglycerides, oxidative stress, and dysregulation of insulin pathway–related genes. QEYO significantly ameliorated these abnormalities in a dose-dependent manner. The 62.5 mg dose produced stronger glucose-lowering effects, while the 125 mg dose showed greater antioxidant enhancement and improved expression of SOD, CAT, IRS, and DILP2. Metformin produced comparable metabolic benefits.

Discussion

QEYO improved glucose homeostasis, lipid metabolism, and insulin pathway activity, and reduced markers of insulin resistance and oxidative imbalance in HSD-induced flies. These findings support its potential as a functional food–based intervention for T2DM and correspond with its traditional role in Chinese dietary therapy for metabolic regulation. Further mammalian studies are required for translational confirmation.
2型糖尿病(T2DM)在全球范围内呈上升趋势,这就产生了对天然和功能性食物治疗干预措施的需求。鹌鹑蛋黄油(QEYO),传统上在中医中被用作养阴和维持代谢平衡(ānchún dànhuáng yóu),含有生物活性脂质和抗氧化剂,与血糖和氧化还原调节有潜在的相关性。本研究探讨了QEYO在高糖饮食(HSD)诱导的黑腹果蝇代谢功能障碍模型中的抗糖尿病和抗氧化作用。方法采用高糖(30%蔗糖)饲粮诱导黑腹果蝇代谢功能障碍,分为对照组、HSD组、QEYO组(62.5或125 mg/10 mL饲粮)和二甲双胍组(16 mg/10 mL)。HSD诱导14天后,治疗7天后,采用酶法和RT-qPCR检测小鼠的生理参数、葡萄糖和脂质生物标志物、氧化应激指标以及关键代谢基因的表达。结果sd喂养的果蝇出现肥胖、高血糖、甘油三酯升高、氧化应激和胰岛素通路相关基因失调。QEYO以剂量依赖性的方式显著改善了这些异常。62.5 mg剂量具有较强的降血糖作用,而125 mg剂量具有较强的抗氧化增强作用,并能提高SOD、CAT、IRS和DILP2的表达。二甲双胍产生了类似的代谢益处。qeyo改善了hsd诱导的果蝇的葡萄糖稳态、脂质代谢和胰岛素途径活性,并降低了胰岛素抵抗和氧化失衡的标志物。这些发现支持其作为功能性食物干预T2DM的潜力,并符合其在中国饮食疗法中代谢调节的传统作用。需要进一步的哺乳动物研究来证实其转化作用。
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引用次数: 0
Multi-target immunomodulatory actions of Elaeagnus rhamnoides L.) A. Nelson phytocompounds on immune regulatory targets via integrative network pharmacology, docking, and molecular simulation 沙棘的多靶点免疫调节作用A. Nelson植物化合物对免疫调节靶点的综合网络药理学、对接和分子模拟
Pub Date : 2026-03-01 Epub Date: 2025-11-29 DOI: 10.1016/j.prmcm.2025.100726
Venkatesan Karthick , Dinesh Kumar Venkatachalam , Singamoorthy Amalraj , Rajkumar Thamarai , Varghese Edwin Hillary , Elsa Shibu Sruthy

Introduction

Elaeagnus rhamnoides (sea buckthorn; 沙棘 Shāji) has long been valued in Chinese traditional medicine as fruit purees, decoctions, and polysaccharide granules for enhancing immunity, treating chronic cough, nourishing yin, and promoting digestive and cardiovascular health. However, the precise immunomodulatory mechanisms of its bioactive compounds remain inadequately understood.

Methods

This study comprehensively evaluated key phytocompounds from E. rhamnoides using network pharmacology and in silico computational analysis. Network pharmacology and molecular docking were applied to evaluate interactions with immune checkpoint proteins CTLA-4 (1AH1) and LAG-3 (7TZG). Electronic properties were assessed using density functional theory (DFT) calculations of HOMO–LUMO energy gaps. Molecular dynamics (MD) simulations and MM-GBSA analyses assessed protein–ligand stability and binding energies. ProTox-II toxicity profiling and network pharmacology further elucidated safety and biological pathway associations.

Results

All selected phytocompounds showed strong binding affinities with CTLA-4 and LAG-3, with narcissin, tellimagrandin I, and astragalin demonstrating the most favourable docking scores and molecular interactions. DFT analysis revealed low HOMO–LUMO gaps (3.76–4.82 eV) for strictinin and tellimagrandin I (high chemical reactivity) and higher kinetic stability for astragalin and narcissin. MD simulations confirmed the stability of astragalin complexes, and MM-GBSA revealed that hydrophobic packing and van der Waals forces were the primary drivers of binding affinity. ProTox-II predicted generally low risks of organ toxicity for all compounds. Network pharmacology showed these phytochemicals target multiple core immune-regulatory genes (including NFB1, HIF1A, MAOA, and TLR4) and are involved in critical immunological pathways such as NF-κB, cytokine signalling, and the PD-1/PD-L1 axis.

Discussion

This study provides the first comprehensive in silico systems pharmacology analysis of E. rhamnoides phytocompounds as multi-target, low-toxicity immunomodulators, supporting traditional Chinese medicine applications. The strong and stable binding to immune checkpoints, favorable electronic properties, and multi-pathway engagement reinforce their promise as plant-based immunotherapeutics. These findings support further experimental validation and recommend the featured E. rhamnoides phytocompounds as promising multi-target leads for the development of novel immunomodulatory therapeutics in modern and traditional Chinese medicine contexts.
IntroductionElaeagnus人体(沙棘;沙棘Shāji)长期以来一直重视中药的果浆,汤,和多糖颗粒增强免疫力,治疗慢性咳嗽、滋养阴,促进消化系统和心血管健康。然而,其生物活性化合物的精确免疫调节机制仍不充分了解。方法采用网络药理学和计算机计算方法对沙棘中主要化合物进行综合评价。应用网络药理学和分子对接技术评价与免疫检查点蛋白CTLA-4 (1AH1)和LAG-3 (7TZG)的相互作用。利用密度泛函理论(DFT)计算HOMO-LUMO能隙来评估电子性质。分子动力学(MD)模拟和MM-GBSA分析评估了蛋白质配体的稳定性和结合能。ProTox-II毒性分析和网络药理学进一步阐明了安全性和生物学途径的关联。结果所选化合物均与CTLA-4和LAG-3具有较强的结合亲和性,其中水仙素、黄芪甲苷和黄芪甲苷的对接得分和分子相互作用最高。DFT分析结果显示,黄芪甲苷和水仙苷I的HOMO-LUMO间隙较低(3.76 ~ 4.82 eV),具有较高的化学反应活性,黄芪甲苷和水仙苷具有较高的动力学稳定性。MD模拟证实了黄芪甲苷配合物的稳定性,MM-GBSA显示疏水堆积和范德华力是结合亲和力的主要驱动因素。ProTox-II预测所有化合物的器官毒性风险一般较低。网络药理学显示,这些植物化学物质靶向多个核心免疫调节基因(包括NFB1、HIF1A、MAOA和TLR4),并参与关键的免疫通路,如NF-κB、细胞因子信号传导和PD-1/PD-L1轴。本研究首次在计算机系统中全面分析了沙棘属植物化合物作为多靶点、低毒的免疫调节剂,支持中药应用。与免疫检查点的强而稳定的结合,有利的电子特性和多途径参与增强了它们作为基于植物的免疫治疗药物的前景。这些发现支持进一步的实验验证,并推荐具有特色的沙棘植物化合物作为在现代和传统医学背景下开发新型免疫调节疗法的有前途的多靶点先导物。
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引用次数: 0
Multitarget insights into traditional Chinese phytoconstituents against tuberculosis via network pharmacology, molecular docking, and MD simulation 通过网络药理学、分子对接和MD模拟研究中药抗结核多靶点
Pub Date : 2025-12-01 Epub Date: 2025-09-20 DOI: 10.1016/j.prmcm.2025.100695
Deepthi D Kini , Tathagata Dey , G Divya Theja , S. Shalini , R. Ruthicshaw , Keshava Murthy SG

Introduction

Tuberculosis (TB), caused by Mycobacterium tuberculosis, is a global health threat. Traditional Chinese medicine (TCM), with its extensive use of plant-based compounds, offers a promising alternative for TB treatment. However, the molecular mechanisms underlying the effects of TCM phytoconstituents on TB have not been fully elucidated. This study aims to explore the multitarget therapeutic potential of TCM phytoconstituents for TB management using network pharmacology, molecular docking, and molecular dynamics (MD) simulations.

Methods

Network pharmacology was employed to identify the interactions between phytoconstituents and proteins associated with TB. Molecular docking evaluated compound binding to key TB targets, while MD simulations assessed complex stability and dynamics. Gene expression was analyzed using the eFP server, and mycoCSM predicted bacterial protein responses to compounds, indicating potential drug resistance or susceptibility.

Results

Network pharmacology analysis identified key biological pathways, including the prolactin signalling pathway and the phosphatidylinositol 3-kinase signalling, that may be modulated by these compounds. The docking scores range from -6.5 to -9.0 kcal/mol for Glabroisoflavanone A and B against three major proteins, viz. 1O43, 5XGI, and 6NJS. Both phytoconstituents exhibited a good anti-tubercular sensitivity score. MD simulations (200 ns) further revealed that Glabroisoflavanone A formed the most stable complex with 5XGI.

Discussion

The Glabroisoflavanone A-5XGI complex showed the strongest binding, supported by the most binding free energy (–75.19 ± 4.89 kcal/mol), suggesting a robust interaction. These findings highlight the differential binding and dynamic behavior of phytoconstituents, offering potential insights for therapeutic development.
由结核分枝杆菌引起的结核病是一种全球性的健康威胁。传统中药(TCM)广泛使用植物基化合物,为结核病治疗提供了一个有希望的替代方案。然而,中药植物成分治疗结核的分子机制尚未完全阐明。本研究旨在通过网络药理学、分子对接和分子动力学(MD)模拟,探索中药植物成分在结核病治疗中的多靶点治疗潜力。方法采用网络药理学方法鉴定结核相关蛋白与植物成分的相互作用。分子对接评估了化合物与关键结核靶点的结合,而MD模拟评估了复合物的稳定性和动力学。使用eFP服务器分析基因表达,mycoCSM预测细菌对化合物的蛋白质反应,表明潜在的耐药性或易感性。结果网络药理学分析确定了这些化合物可能调节的关键生物学通路,包括催乳素信号通路和磷脂酰肌醇3-激酶信号通路。Glabroisoflavanone A和B对3种主要蛋白(即1043、5XGI和6NJS)的对接分数在-6.5 ~ -9.0 kcal/mol之间。两种植物成分均表现出良好的抗结核敏感性评分。MD模拟(200 ns)进一步表明,光异黄酮A与5XGI形成了最稳定的配合物。Glabroisoflavanone a - 5xgi配合物结合最强,结合自由能最高(-75.19±4.89 kcal/mol),表明其相互作用强。这些发现突出了植物成分的差异结合和动态行为,为治疗开发提供了潜在的见解。
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引用次数: 0
Therapeutic potential of flavonoid-enriched Chinese medicinal herbs in atherosclerosis, hypertension, myocardial infarction, and heart failure 富含类黄酮的中草药对动脉粥样硬化、高血压、心肌梗死和心力衰竭的治疗潜力
Pub Date : 2025-12-01 Epub Date: 2025-10-01 DOI: 10.1016/j.prmcm.2025.100701
Dharshini Jaisankar, Suruthi Ramamoorthy, Jubilee Ramasamy

Introduction

CVDs such as atherosclerosis, hypertension, myocardial infarction, and heart failure, are the top cause of death worldwide. Due to the challenges with traditional therapies, interest in complementary treatments has increased. Research has found that TCM and its herbal constituents, rich in flavonoids, appear to have a positive effect on cardiovascular health due to several underlying mechanisms.

Methods

This review provides an overview of current clinical and experimental research on flavonoid-rich Chinese medicinal plants. The database includes PubMed, Scopus, Web of Science, and CNKI. Details include various cardiovascular diseases (CVD) types and their mechanism of action (including antioxidant, anti-inflammation, enhancement of endothelial function, and stabilization of mitochondria). It also features studies of several compounds in preclinical models and clinical trials, including quercetin and baicalin as key representatives. Significant portion pathways are PI3K/AKT, NF-κB, Nrf2/HO-1, eNOS and AMPK/mTOR. The comparative table highlights plants, pharmaceutical targets, and the impact of diseases.

Result

Evidence suggests that flavonoids from Chinese medicinal plants have a wide-ranging cardio-protective effect, regardless of the CVD model. The compounds possess potent antioxidant, anti-inflammatory, endothelial-enhancing, and lipid-regulatory effects. While recent clinical studies indicate improvements in blood pressure, lipid profiles, myocardial resilience, and endothelial function, results remain inconsistent due to small sample size, differences in extract composition, and variation in trial design.

Discussion

The use of Chinese medicinal herbs enriched in flavonoids can provide effective multi-pathway intervention against complex pathophysiological mechanisms, making them a valuable resource for cardiovascular therapy. Despite the obvious translational potential, shortcomings like poor bioavailability, phytochemical variability, and limited clinical trials are significant. These limitations continue to hinder clinical translation, and addressing them will be critical for broder therapeutic adoption. Future research should focus on improving the formulation, facilitating clinical standardization, and developing systems-level pharmacology to enable evidence-based use of flavonoid therapies in modern cardiovascular medicine.
心血管疾病,如动脉粥样硬化、高血压、心肌梗死和心力衰竭,是全世界最主要的死亡原因。由于传统疗法的挑战,对补充疗法的兴趣增加了。研究发现,中药及其富含类黄酮的草药成分似乎对心血管健康有积极的影响,这是由于几种潜在的机制。方法综述了近年来富含类黄酮的中药材的临床和实验研究进展。数据库包括PubMed、Scopus、Web of Science和CNKI。详细内容包括各种心血管疾病(CVD)类型及其作用机制(包括抗氧化、抗炎症、增强内皮功能和稳定线粒体)。以槲皮素和黄芩苷为主要代表,对几种化合物进行了临床前模型和临床试验研究。PI3K/AKT、NF-κB、Nrf2/HO-1、eNOS和AMPK/mTOR通路占显著比例。比较表突出了植物、药物靶点和疾病的影响。结果有证据表明,无论心血管疾病模型如何,中草药类黄酮都具有广泛的心脏保护作用。这些化合物具有有效的抗氧化、抗炎、内皮增强和脂质调节作用。虽然最近的临床研究表明血压、血脂、心肌恢复力和内皮功能有所改善,但由于样本量小、提取物成分不同以及试验设计的差异,结果仍然不一致。富含黄酮类化合物的中草药可对复杂的病理生理机制提供有效的多途径干预,是心血管治疗的宝贵资源。尽管有明显的转化潜力,但生物利用度差、植物化学变异性和有限的临床试验等缺点是显著的。这些限制继续阻碍临床转化,解决它们对于更广泛的治疗采用至关重要。未来的研究应着眼于改进黄酮类药物的处方,促进临床标准化,发展系统级药理学,使黄酮类药物在现代心血管医学中的循证应用成为可能。
{"title":"Therapeutic potential of flavonoid-enriched Chinese medicinal herbs in atherosclerosis, hypertension, myocardial infarction, and heart failure","authors":"Dharshini Jaisankar,&nbsp;Suruthi Ramamoorthy,&nbsp;Jubilee Ramasamy","doi":"10.1016/j.prmcm.2025.100701","DOIUrl":"10.1016/j.prmcm.2025.100701","url":null,"abstract":"<div><h3>Introduction</h3><div>CVDs such as atherosclerosis, hypertension, myocardial infarction, and heart failure, are the top cause of death worldwide. Due to the challenges with traditional therapies, interest in complementary treatments has increased. Research has found that TCM and its herbal constituents, rich in flavonoids, appear to have a positive effect on cardiovascular health due to several underlying mechanisms.</div></div><div><h3>Methods</h3><div>This review provides an overview of current clinical and experimental research on flavonoid-rich Chinese medicinal plants. The database includes PubMed, Scopus, Web of Science, and CNKI. Details include various cardiovascular diseases (CVD) types and their mechanism of action (including antioxidant, anti-inflammation, enhancement of endothelial function, and stabilization of mitochondria). It also features studies of several compounds in preclinical models and clinical trials, including quercetin and baicalin as key representatives. Significant portion pathways are PI3K/AKT, NF-κB, Nrf2/HO-1, eNOS and AMPK/mTOR. The comparative table highlights plants, pharmaceutical targets, and the impact of diseases.</div></div><div><h3>Result</h3><div>Evidence suggests that flavonoids from Chinese medicinal plants have a wide-ranging cardio-protective effect, regardless of the CVD model. The compounds possess potent antioxidant, anti-inflammatory, endothelial-enhancing, and lipid-regulatory effects. While recent clinical studies indicate improvements in blood pressure, lipid profiles, myocardial resilience, and endothelial function, results remain inconsistent due to small sample size, differences in extract composition, and variation in trial design.</div></div><div><h3>Discussion</h3><div>The use of Chinese medicinal herbs enriched in flavonoids can provide effective multi-pathway intervention against complex pathophysiological mechanisms, making them a valuable resource for cardiovascular therapy. Despite the obvious translational potential, shortcomings like poor bioavailability, phytochemical variability, and limited clinical trials are significant. These limitations continue to hinder clinical translation, and addressing them will be critical for broder therapeutic adoption. Future research should focus on improving the formulation, facilitating clinical standardization, and developing systems-level pharmacology to enable evidence-based use of flavonoid therapies in modern cardiovascular medicine.</div></div>","PeriodicalId":101013,"journal":{"name":"Pharmacological Research - Modern Chinese Medicine","volume":"17 ","pages":"Article 100701"},"PeriodicalIF":0.0,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145268679","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Unveiling macrophage-centric immunomodulatory mechanisms of radix salviae miltiorrhizae in abdominal aortic aneurysm through integrated single-cell transcriptomic, network pharmacological, and molecular docking analyses 通过单细胞转录组学、网络药理学和分子对接分析揭示丹参对腹主动脉瘤巨噬细胞的免疫调节机制
Pub Date : 2025-12-01 Epub Date: 2025-09-25 DOI: 10.1016/j.prmcm.2025.100694
Xinru Zheng , Runyu Gan , Jingxian Wu , Ruili Xue , Chaoyi Cui , Yuyin Duan
<div><h3>Background</h3><div>Abdominal aortic aneurysm (AAA) represents a fatal vascular disease with prevalence rates of 4–8 % among individuals over 65 years, and rupture mortality rates reaching 60–80 %. With accelerating population aging, AAA incidence continues rising, creating urgent demands for novel therapeutic strategies. Current treatments including surgical intervention and endovascular therapy, while effective, demonstrate significant limitations, and the pathogenic mechanisms remain unclear. The inflammatory microenvironment and macrophages play crucial roles in AAA, yet their immune mechanisms remain controversial. The advancement of single-cell sequencing technology provides new opportunities for elucidating AAA immune mechanisms. This study employed single-cell RNA sequencing (scRNA-seq) and network pharmacology to characterize immune cell features and identify therapeutic targets, exploring the immunomodulatory effects of Radix Salviae miltiorrhizae (RS), aiming to reveal AAA pathogenic mechanisms and provide novel precision treatment strategies.</div></div><div><h3>Method</h3><div>Using scRNA-seq data from healthy and AAA mouse models in the GEO database (GSE239620), we performed preprocessing and quality control through Seurat, employed Harmony to correct batch effects, and combined clustering, pseudotemporal analysis (Monocle2), and cell communication analysis (CellChat) to reveal the characteristics and interactions of immune cells, particularly macrophages, within the AAA inflammatory microenvironment. Network pharmacology utilized TCMSP and SwissADME to screen active components and targets of RS, with molecular docking (AutoDock Vina) validating their binding to target proteins. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses (clusterProfiler) elucidated biological functions. This study integrates scRNA-seq and network pharmacology to explore AAA immune mechanisms and RS therapeutic potential.</div></div><div><h3>Result</h3><div>This study investigated the immune microenvironment of AAA via scRNA-seq, elucidating the pivotal role of macrophages in disease progression. UMAP clustering identified five distinct immune cell types, revealing a significant enrichment of macrophages in AAA samples (<em>P</em> < 0.01). Subsequent sub-clustering analysis distinguished five macrophage subtypes (Mac1–Mac5), each characterized by a unique marker gene expression profile (logFC > 0.5, <em>P</em> < 0.05). Pseudotime analysis using Monocle2 mapped their developmental trajectories and identified key gene modules associated with immune responses and inflammatory regulation (<em>q</em> < 0.1). Furthermore, cell communication analysis with CellChat indicated enhanced interactions between macrophages and T/NK cells, underscored by the robust activation of MHC-I signaling (communication probability > 0.5). GO and KEGG analyses showed that associated genes were primarily enriched in the “re
腹主动脉瘤(AAA)是一种致命的血管疾病,在65岁以上的人群中患病率为4 - 8%,破裂死亡率达到60 - 80%。随着人口老龄化的加速,AAA发病率持续上升,迫切需要新的治疗策略。目前的治疗方法包括手术干预和血管内治疗,虽然有效,但有很大的局限性,而且发病机制尚不清楚。炎症微环境和巨噬细胞在AAA中起关键作用,但其免疫机制仍有争议。单细胞测序技术的进步为阐明AAA免疫机制提供了新的机会。本研究采用单细胞RNA测序(scRNA-seq)和网络药理学方法表征免疫细胞特征,鉴定治疗靶点,探索丹参(RS)的免疫调节作用,旨在揭示AAA致病机制,提供新的精准治疗策略。方法利用GEO数据库(GSE239620)中健康小鼠和AAA小鼠模型的scRNA-seq数据,通过Seurat进行预处理和质量控制,使用Harmony进行批次效应校正,并结合聚类、伪时间分析(Monocle2)和细胞通讯分析(CellChat)来揭示AAA炎症微环境中免疫细胞,特别是巨噬细胞的特征和相互作用。网络药理学利用TCMSP和SwissADME筛选RS的活性成分和靶点,并通过分子对接(AutoDock Vina)验证其与靶蛋白的结合。基因本体(GO)和京都基因与基因组百科全书(KEGG)富集分析(clusterProfiler)阐明了生物功能。本研究将scRNA-seq和网络药理学相结合,探索AAA免疫机制和RS治疗潜力。结果本研究通过scRNA-seq研究了AAA的免疫微环境,阐明了巨噬细胞在疾病进展中的关键作用。UMAP聚类鉴定出五种不同的免疫细胞类型,揭示了AAA样品中巨噬细胞的显著富集(P < 0.01)。随后的亚聚类分析区分了五种巨噬细胞亚型(Mac1-Mac5),每种亚型都具有独特的标记基因表达谱(logFC > 0.5, P < 0.05)。使用Monocle2进行伪时间分析,绘制了它们的发育轨迹,并确定了与免疫反应和炎症调节相关的关键基因模块(q < 0.1)。此外,CellChat的细胞通讯分析表明,巨噬细胞与T/NK细胞之间的相互作用增强,MHC-I信号的强大激活强调了这一点(通讯概率>; 0.5)。GO和KEGG分析显示,相关基因主要富集于“调节先天免疫反应”(P < 0.01)和“脂质与动脉粥样硬化”途径(P < 0.05),网络药理学筛选了RS的有效成分,分子对接发现木犀草素对TNF具有最强的结合亲和力(-8.6 kcal/mol),提示其具有治疗潜力。本研究通过scRNA-seq和网络药理学分析和预测了巨噬细胞在AAA中潜在的关键作用,表明巨噬细胞与T/NK细胞的相互作用增强,在炎症通路中富集。生物活性化合物木犀草素通过计算预测了与TNF的强结合亲和力(-8.6 kcal/mol),表明其具有治疗潜力。
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引用次数: 0
Mechanistic insights into the neuroprotective effects of Radix Astragali (Huang Qi): Bridging Traditional Chinese Medicine and modern pharmacology 黄芪神经保护作用的机理研究:中医与现代药理学的桥梁
Pub Date : 2025-12-01 Epub Date: 2025-10-24 DOI: 10.1016/j.prmcm.2025.100711
Rizwan Ahmad , Chhavi Verma , Sandeep Kumar , Vishal Kumar , Darakhshan Gazala Bari , Saurabh Sharma , Shadab Ali , Shamim Shamim

Introduction

Radix Astragali, a major herb in Traditional Chinese Medicine, has traditionally been used to strengthen vital energy and promote blood circulation. Recent research has revealed its neuroprotective potential in disorders such as ischemic stroke, Alzheimer’s disease, and traumatic brain injury.

Methods

This review evaluates recent preclinical and clinical studies on the neuroprotective effects of Radix Astragali and its active components, including astragaloside four, flavonoids, polysaccharides, terpenoids, alkaloids, and amino acids. Peer-reviewed scientific literature was analyzed and interpreted within the context of Traditional Chinese Medicine principles.

Results

Radix Astragali exhibits multiple neuroprotective actions, including antioxidant, anti-inflammatory, anti-apoptotic, and immune-regulating effects. Astragaloside IV regulates critical signaling pathways, including phosphoinositide 3-kinase/protein kinase B, mitogen-activated protein kinase, and nuclear factor-κB, thereby supporting neuronal survival and reducing oxidative damage. Flavonoids and polysaccharides enhance synaptic plasticity, nerve regeneration, and cerebral blood flow. These findings are consistent with Traditional Chinese Medicine concepts of replenishing vital energy and stimulating blood flow in neurological disorders.

Discussion

Radix Astragali exemplifies the integration of Traditional Chinese Medicine and modern neuropharmacology. However, clinical translation remains limited due to challenges in standardization, potential herb drug interactions, and insufficient large-scale clinical validation. Future studies should emphasize pharmacokinetics, synergistic formulations, and biomarker-based personalized neurotherapy to ensure safe and effective clinical application.
黄芪是一种重要的中药,传统上被用来增强元气,促进血液循环。最近的研究表明,它在缺血性中风、阿尔茨海默病和创伤性脑损伤等疾病中具有神经保护作用。方法综述了近年来黄芪及其有效成分黄芪甲苷、黄酮类、多糖、萜类、生物碱和氨基酸等神经保护作用的临床前和临床研究。同行评议的科学文献在中医原理的背景下进行分析和解释。结果黄芪具有抗氧化、抗炎、抗凋亡、免疫调节等多种神经保护作用。黄芪甲苷调节磷酸肌苷3-激酶/蛋白激酶B、丝裂原活化蛋白激酶、核因子-κB等关键信号通路,支持神经元存活,减少氧化损伤。黄酮类化合物和多糖增强突触可塑性、神经再生和脑血流量。这些发现与传统中医在神经系统疾病中补充元气和刺激血液流动的概念是一致的。黄芪是中医与现代神经药理学相结合的典范。然而,由于标准化、潜在的中草药相互作用和大规模临床验证不足的挑战,临床翻译仍然有限。未来的研究应强调药代动力学、协同配方和基于生物标志物的个性化神经治疗,以确保安全有效的临床应用。
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引用次数: 0
Re: Progress in the application of AI in the standardization of traditional Chinese medicine: Discussion and prospects 人工智能在中医标准化中的应用进展:讨论与展望
Pub Date : 2025-12-01 Epub Date: 2025-09-06 DOI: 10.1016/j.prmcm.2025.100681
James O. Fajemiroye
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引用次数: 0
Integrated network, docking, and experimental validation of the dual anti-inflammatory and uricosuric actions of Artemisia vulgaris compounds 青蒿类化合物抗炎、尿双重作用的整合网络、对接及实验验证
Pub Date : 2025-12-01 Epub Date: 2025-10-25 DOI: 10.1016/j.prmcm.2025.100712
Pham Thi Nhat Trinh , Dang Thi Le Hang , Nguyen Ngoc Phuong Uyen , Tran Nguyen Minh An , Le Xuan Tien , Le Tien Dung
In Traditional Chinese Medicine (TCM), mugwort (Artemisia vulgaris) is documented as the primary material for moxibustion, prepared as moxa floss (ai rong, 艾绒), moxa cones (ai zhu, 艾炷), and moxa sticks (ai tiao, 艾条) to warm the channels and regulate qi–blood [6–8]. We therefore investigated A. vulgaris compounds for multi-target anti-gout relevance, anchored in these TCM indications.
Network pharmacology and molecular docking prioritized A. vulgaris phytochemicals against gout-related targets, followed by in-vitro validation in LPS-challenged RAW 264.7 macrophages.
Of 62 compounds, 52 met drug-likeness and intersected 277 gout genes. A flavonoid (AV52) showed strong predicted binding to PTGS2/XO, and artemisinin (AV46) to urate transporters (SLC22A12/ABCG2). Experimentally, AV46 reduced IL-6/TNF-α and nitrite while preserving IL-10. IL-10 showed a small, non-monotonic change at 6.25 µM (p < 0.05) that was not reproduced at adjacent doses, suggesting limited biological relevance, while overall IL-10 was preserved alongside reductions in IL-6 and TNF-α.
Framed within TCM practice of moxibustion and warming/qi–blood-regulating indications, these data support a lead–anchor concept (AV52 anti-inflammatory/XO; AV46 uricosuric-anti-inflammatory) warranting further in-vivo and formulation studies for TCM-relevant applications.
A. vulgaris phytochemicals demonstrate complementary potential against gout-related inflammation and urate handling within a TCM use-case anchored to mugwort preparations (moxa floss/cones/sticks). AV46 showed experimental activity consistent with predictions, while AV52 requires bench confirmation. These results motivate focused biochemical, transporter, pharmacokinetic, and in-vivo evaluations to support translation into Chinese preparation - compatible applications.
在中医中,艾草(Artemisia vulgaris)被记载为艾灸的主要原料,制成艾牙线(艾蓉,绒)、艾球茎(艾朱,炷)和艾条(艾条,),以温经、调气血[6-8]。因此,我们研究了寻常草化合物的多靶点抗痛风相关性,锚定在这些中医适应症中。网络药理学和分子对接优先考虑了A. vulgaris植物化学物质对痛风相关靶点的作用,随后在lps挑战的RAW 264.7巨噬细胞中进行了体外验证。62个化合物中,52个与药物相似,并与277个痛风基因交叉。类黄酮(AV52)与PTGS2/XO结合,青蒿素(AV46)与尿酸转运蛋白(SLC22A12/ABCG2)结合。实验表明,AV46降低IL-6/TNF-α和亚硝酸盐,同时保留IL-10。IL-10在6.25µM (p < 0.05)时表现出小的非单调变化,在相邻剂量下没有重现,表明有限的生物学相关性,而IL-10总体上与IL-6和TNF-α的减少保持一致。在中医艾灸和温热/气血调节适应症的框架下,这些数据支持了一个铅锚概念(AV52抗炎/XO; AV46抗尿-抗炎),为中医相关应用的进一步体内和配方研究提供了依据。在艾草制剂(艾牙线/艾锥/艾棒)的中医用例中,vulgaris植物化学物质显示出对抗痛风相关炎症和尿酸处理的互补潜力。AV46的实验活动与预测一致,而AV52则需要实验验证。这些结果激发了集中的生化,转运体,药代动力学和体内评价,以支持翻译成中国制剂兼容的应用。
{"title":"Integrated network, docking, and experimental validation of the dual anti-inflammatory and uricosuric actions of Artemisia vulgaris compounds","authors":"Pham Thi Nhat Trinh ,&nbsp;Dang Thi Le Hang ,&nbsp;Nguyen Ngoc Phuong Uyen ,&nbsp;Tran Nguyen Minh An ,&nbsp;Le Xuan Tien ,&nbsp;Le Tien Dung","doi":"10.1016/j.prmcm.2025.100712","DOIUrl":"10.1016/j.prmcm.2025.100712","url":null,"abstract":"<div><div>In Traditional Chinese Medicine (TCM), mugwort (<em>Artemisia vulgaris</em>) is documented as the primary material for moxibustion, prepared as moxa floss (<em>ai rong</em>, 艾绒), moxa cones (<em>ai zhu</em>, 艾炷), and moxa sticks (<em>ai tiao</em>, 艾条) to warm the channels and regulate qi–blood [6–8]. We therefore investigated <em>A. vulgaris</em> compounds for multi-target anti-gout relevance, anchored in these TCM indications.</div><div>Network pharmacology and molecular docking prioritized A. vulgaris phytochemicals against gout-related targets, followed by in-vitro validation in LPS-challenged RAW 264.7 macrophages.</div><div>Of 62 compounds, 52 met drug-likeness and intersected 277 gout genes. A flavonoid (AV52) showed strong predicted binding to PTGS2/XO, and artemisinin (AV46) to urate transporters (SLC22A12/ABCG2). Experimentally, AV46 reduced IL-6/TNF-α and nitrite while preserving IL-10. IL-10 showed a small, non-monotonic change at 6.25 µM (<em>p</em> &lt; 0.05) that was not reproduced at adjacent doses, suggesting limited biological relevance, while overall IL-10 was preserved alongside reductions in IL-6 and TNF-α.</div><div>Framed within TCM practice of moxibustion and warming/qi–blood-regulating indications, these data support a lead–anchor concept (AV52 anti-inflammatory/XO; AV46 uricosuric-anti-inflammatory) warranting further in-vivo and formulation studies for TCM-relevant applications.</div><div>A. vulgaris phytochemicals demonstrate complementary potential against gout-related inflammation and urate handling within a TCM use-case anchored to mugwort preparations (moxa floss/cones/sticks). AV46 showed experimental activity consistent with predictions, while AV52 requires bench confirmation. These results motivate focused biochemical, transporter, pharmacokinetic, and in-vivo evaluations to support translation into Chinese preparation - compatible applications.</div></div>","PeriodicalId":101013,"journal":{"name":"Pharmacological Research - Modern Chinese Medicine","volume":"17 ","pages":"Article 100712"},"PeriodicalIF":0.0,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145417214","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Chinese herbal medicine Quxie formula inhibits colon cancer liver metastasis through modulating gut Actinobacteria induced apoptosis and anti-cancer immunity 中药祛邪方通过调节肠道放线菌诱导的细胞凋亡和抗癌免疫抑制结肠癌肝转移
Pub Date : 2025-12-01 Epub Date: 2025-11-21 DOI: 10.1016/j.prmcm.2025.100724
Yunzi Yan , Bo Feng , Jake Mao , Chunhui Ning , Yufei Yang , Lingyun Sun

Objective

Liver metastasis is the leading cause of mortality in colon cancer patients. Traditional Chinese herbal medicine Quxie formula (QX) has been shown to prolong survival, improve immune function and modulate the gut microbiome, particularly increasing Actinobacteria in metastatic colorectal cancer (mCRC) patients. However, the mechanism remains unclear.

Methods

In Vitro, QX-containing serum was extracted from rats and used to culture three Actinobacteria strains: Bifidobacterium adolescentis (B. a.), Streptomyces carpaticus, and Bacillus. After screening for bacterial growth, QX-B. a. co-culture products were applied to HCT-116 cells to assess apoptosis and apoptosis-related protein expression. Caspase3, Caspase8, and Caspase9 pathways were blocked to further investigate apoptosis mechanisms. We then established a CT-26 liver metastasis mouse model pretreated with cocktail antibiotics, followed by 14-day QX decoction treatment. Liver tissue, immune function, cytokine, and gut microbiome were analyzed using Western blotting (WB), flow cytometry analysis, ELISA and 16S rRNA sequencing, respectively.

Results

In Vitro, QX-containing serum significantly promoted B. a. proliferation, and the QX-B. a. co-culture products induced higher apoptosis rates in HCT-116 cells than controls. WB results showed increased expression of Caspase3, Caspase8, Caspase9, Bax, and Bid, and decreased Bcl-2 expression in QX-B. a. co-culture groups. Blocking Caspase3, Caspase8, and Caspase9 significantly reduced apoptosis, confirming the Bcl-2/Bax pathway’s involvement. In Vivo, 10 mg, 15 mg, and 20 mg daily QX treatment significantly reduced liver metastasis tumor burden. QX treatment increased gut Actinobacteria, Bacteroidetes, and Firmicutes abundance compared to model groups. QX significantly enhanced the protein expression of Caspase3, Caspase8 and Caspase9 in liver metastatic tissues. Compared to model group, QX could significantly enhance the proportion of CD8+, expression of TNF-α and IFN-γ in peripheral blood. In liver metastatic tissue, QX could restore the NK cells’ ability of targeting and killing cancer cells. Through UPLC-Q-TOF-MSE analysis, 69 molecular compounds were preliminarily identified in the decoction of QX and medicated serum.

Conclusion

This study provides new insights into the gut microbiome-mediated anti-cancer effects of QX, warranting further investigation into its active components and therapeutic mechanism.
目的肝癌转移是结肠癌患者死亡的主要原因。中药祛泻方(QX)已被证明可以延长转移性结直肠癌(mCRC)患者的生存期,提高免疫功能,调节肠道微生物群,特别是增加放线菌群。然而,其机制尚不清楚。方法体外提取含qx的大鼠血清,培养3株放线菌:青少年双歧杆菌(b.a .)、carpaticus链霉菌和芽孢杆菌。筛选细菌生长后,QX-B。a.共培养产物应用于HCT-116细胞,评估细胞凋亡和凋亡相关蛋白的表达。阻断Caspase3、Caspase8和Caspase9通路,进一步研究凋亡机制。建立CT-26肝转移小鼠模型,先用鸡尾酒抗生素预处理,再用芪x汤治疗14 d。分别采用Western blotting (WB)、流式细胞术、ELISA和16S rRNA测序分析肝组织、免疫功能、细胞因子和肠道微生物组。结果在体外,含qx血清能显著促进B. a.的增殖;a.共培养产物诱导HCT-116细胞的凋亡率高于对照组。WB结果显示,QX-B中Caspase3、Caspase8、Caspase9、Bax、Bid表达增加,Bcl-2表达降低。A.共同文化群体。阻断Caspase3、Caspase8和Caspase9显著减少凋亡,证实了Bcl-2/Bax通路的参与。在体内,每日10mg、15mg和20mg QX治疗可显著减轻肝转移瘤负担。与模型组相比,QX治疗增加了肠道放线菌、拟杆菌门和厚壁菌门的丰度。QX显著提高了肝转移组织中Caspase3、Caspase8和Caspase9蛋白的表达。与模型组比较,芪x能显著提高大鼠外周血CD8+比例、TNF-α、IFN-γ的表达。在肝转移组织中,QX可以恢复NK细胞靶向和杀伤癌细胞的能力。通过UPLC-Q-TOF-MSE分析,初步鉴定出69个分子化合物。结论本研究为QX的肠道微生物介导的抗癌作用提供了新的认识,值得进一步研究其有效成分和治疗机制。
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引用次数: 0
To explore the scientific connotation of Fuyang therapy for liver cancer based on mitochondrial function 探讨基于线粒体功能的肝癌复阳疗法的科学内涵
Pub Date : 2025-12-01 Epub Date: 2025-10-20 DOI: 10.1016/j.prmcm.2025.100709
Yang Wang , Bugao Zhou , Shanshan Li , Linxin Zheng , Bohan Cai , Huiyu Wang , Sili Li , Yuhan Lin , Yanhe Xu

Background

Liver cancer poses a serious threat to human health,and research into its pathogenesis and exploration of treatment strategies have always been major focuses in the medical field.Recent studies have indicated that mitochondrial dysfunction plays a promoting role in the progression of liver cancer,primarily manifested through disruptions in energy metabolism,decreased mitochondrial outer membrane permeability, and dysregulation of calcium ion homeostasis. In traditional Chinese medicine (TCM), “Yang deficiency and Yin excess” is considered the core pathogenesis of liver cancer, and the fundamental treatment principle of “Fuyang Guben” (supporting Yang and reinforcing the root) has been proposed. The mechanism of action may be associated with the improvement of mitochondrial function, however modern research in this area remains relatively limited.

Methods

Through theoretical analysis and comprehensive literature review, this paper elucidates the theoretical basis of Fuyang therapy for liver cancer from the perspective of TCM theory,summarizes the specific roles of mitochondrial function in the progression of liver cancer, and systematically reviews recent advances in modern mechanistic research on how Fuyang therapy inhibits the occurrence and development of liver cancer by regulating mitochondrial function.

Results

Fuyang therapy can improve mitochondrial function from multiple perspectives,including restoring energy metabolism,regulating membrane permeability, and maintaining calcium homeostasis,thereby inhibiting the proliferation and progression of liver cancer cells.Existing experimental and clinical studies have preliminarily verified the potential efficacy of Fuyang-based formulas in anti-liver cancer treatments and their regulatory mechanisms involving mitochondrial function-related pathways.

Conclusion

Fuyang therapy demonstrates both theoretical rationality and experimental support in the treatment of liver cancer.Its anti-liver cancer effects are achieved through the improvement of mitochondrial function,providing new insights for the formulation of TCM-based treatments and mechanistic research on liver cancer.
肝癌严重威胁人类健康,其发病机制的研究和治疗策略的探索一直是医学界关注的焦点。近期研究表明,线粒体功能障碍在肝癌的进展中起促进作用,主要表现为能量代谢紊乱、线粒体外膜通透性降低、钙离子稳态失调。在中医中,“阳虚阴虚”被认为是肝癌的核心病机,并提出了“扶阳固本”(扶阳补根)的基本治疗原则。其作用机制可能与线粒体功能的改善有关,但在这方面的现代研究相对有限。方法通过理论分析和综合文献综述,从中医理论角度阐述阜阳疗法治疗肝癌的理论基础,总结线粒体功能在肝癌进展中的具体作用,系统综述阜阳疗法通过调节线粒体功能抑制肝癌发生发展的现代机制研究最新进展。结果复阳疗法可从恢复能量代谢、调节细胞膜通透性、维持钙稳态等多个角度改善线粒体功能,从而抑制肝癌细胞的增殖和进展。现有的实验和临床研究已经初步验证了阜阳方抗肝癌的潜在疗效及其涉及线粒体功能相关通路的调控机制。结论扶阳法治疗肝癌具有理论合理性和实验依据。其抗肝癌作用是通过改善线粒体功能实现的,为肝癌中药治疗方案的制定和机制研究提供了新的见解。
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引用次数: 0
期刊
Pharmacological Research - Modern Chinese Medicine
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