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Shanxiangyuanye (Turpiniae Folium) for diabetic complications: chemical constituents and therapeutic potential 山香元叶治疗糖尿病并发症的化学成分及治疗潜力
Q3 Medicine Pub Date : 2025-09-01 DOI: 10.1016/j.dcmed.2025.09.012
Ruiyao XIONG , Shuang CHEN , Zihao DAI , Limin GONG

Objective

To analyze the chemical constituents of Shanxiangyuanye (Turpiniae Folium) through liquid chromatography-tandem mass spectrometry (LC-MS/MS) method, and to evaluate their anti-oxidant, hypoglycemic, and anti-glycation activities related to diabetic complications.

Methods

The supernatant of Shanxiangyuanye (Turpiniae Folium) (TFS), obtained following water extraction and alcohol precipitation, was analyzed by LC-MS/MS. Antioxidant activity of TFS in vitro was evaluated using three experimental approaches: the 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging assay, the 2,2’-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS+) radical cation decolorization assay, and the hydroxyl (·OH) radical scavenging assay. To comprehensively evaluate hypoglycemic potential, α-glucosidase inhibition was measured to analyze in vitro hypoglycemic activity. Subsequently, in vitro models were developed to examine anti-glycation activity through the bovine serum albumin (BSA)-fructose (Fru), BSA-methylglyoxal (MGO), BSA-glyoxal (GO), and D-arginine (Arg)-MGO systems, with particular attention to the inhibitory effects of TFS. Furthermore, the concentrations of fructosamine, protein carbonyls, sulfhydryl groups, and β-amyloid in the glycation solution were quantified using the BSA-Fru model following 7-d of incubation at 37 °C.

Results

Using LC-MS/MS analysis in both positive and negative ion modes, we identified 750 chemical components in TFS, primarily including organic acids, amino acids, and their derivatives. In vitro activity studies demonstrated that TFS exhibited remarkable free radical scavenging capacity, with half-maximal inhibitory concentrations (IC50) of 0.47, 1.56, and 0.36 mg/mL against DPPH, ABTS+, and ·OH radicals, respectively. Regarding hypoglycemic activity, TFS dose-dependently inhibited α-glucosidase activity (IC50 = 0.21 mg/mL), displaying comparable efficacy to the clinical drug acarbose (IC50 = 0.23 mg/mL). Notably, TFS intervened in the glycation process: IC50 values were 0.22, 1.91 – 4.96, and 4.09 mg/mL in the BSA-Fru, BSA-MGO/GO, and Arg-MGO models, respectively, with the most prominent inhibitory effects observed in the BSA-Fru model. Furthermore, although TFS may not effectively preserve thiol groups in BSA or reduce thiol oxidation during glycation, it significantly reduces fructosamine levels (in a dose-dependent manner), decreases β-amyloid formation, and inhibits protein carbonylation (P < 0.000 1).

Conclusion

The findings demonstrate that TFS exhibits a complex chemical composition with potent antioxidant, hypoglycemic, and anti-glycation activities. These results provide compelling scientific evidence supporting TFS’s potential as a natural adjuvant for diabetes prevention and complication mana
目的采用液相色谱-串联质谱(LC-MS/MS)方法分析山香元叶的化学成分,并评价其抗氧化、降血糖和抗糖化作用与糖尿病并发症的关系。方法采用液相色谱-质谱联用(LC-MS/MS)对经水提醇沉得到的山香元叶(TFS)上清液进行分析。采用1,1-二苯基-2-吡啶肼基(DPPH)自由基清除实验、2,2 ' -氮基-双(3-乙基苯并噻唑啉-6-磺酸)(ABTS+)自由基阳离子脱色实验和羟基(·OH)自由基清除实验,对TFS的体外抗氧化活性进行了评价。采用α-葡萄糖苷酶抑制法,综合评价其降糖潜能。随后,建立了体外模型,通过牛血清白蛋白(BSA)-果糖(Fru)、BSA-甲基乙二醛(MGO)、BSA-乙二醛(GO)和d -精氨酸(Arg)-MGO系统检测抗糖基化活性,特别关注TFS的抑制作用。此外,37°C孵育7 d后,使用BSA-Fru模型定量糖基化溶液中果糖胺、蛋白羰基、巯基和β-淀粉样蛋白的浓度。结果在正离子和负离子模式下,通过LC-MS/MS分析,我们鉴定出了750种化学成分,主要包括有机酸、氨基酸及其衍生物。体外活性研究表明,TFS具有显著的自由基清除能力,对DPPH、ABTS+和·OH自由基的半最大抑制浓度(IC50)分别为0.47、1.56和0.36 mg/mL。在降糖活性方面,TFS呈剂量依赖性抑制α-葡萄糖苷酶活性(IC50 = 0.21 mg/mL),与临床药物阿卡波糖(IC50 = 0.23 mg/mL)效果相当。值得注意的是,TFS干预糖基化过程:BSA-Fru、BSA-MGO/GO和Arg-MGO模型的IC50值分别为0.22、1.91 - 4.96和4.09 mg/mL,其中BSA-Fru模型的抑制作用最为显著。此外,虽然TFS可能不能有效地保存牛血清白蛋白中的硫醇基团或减少糖基化过程中的硫醇氧化,但它可以显著降低果糖胺水平(以剂量依赖的方式),减少β-淀粉样蛋白的形成,并抑制蛋白质羰基化(P < 0.000 1)。结论TFS具有复杂的化学成分,具有较强的抗氧化、降血糖和抗糖基化活性。这些结果提供了令人信服的科学证据,支持TFS作为糖尿病预防和并发症管理的天然佐剂的潜力,同时为其在功能食品开发和辅助抗糖尿病治疗中的应用奠定了坚实的基础。
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引用次数: 0
Advances and prospects of the integration of multi-omics and artificial intelligence in traditional Chinese medicine research 多组学与人工智能在中药研究中的应用进展与展望
Q3 Medicine Pub Date : 2025-09-01 DOI: 10.1016/j.dcmed.2025.09.003
L.I.U. Guicheng , L.O.N.G. Xi , P.E.N.G. Qinghua , T.I.A.N. Sainan , H.U. Shujuan

Objective

To map the research hotspots, developmental trends, and existing challenges in the integration of artificial intelligence (AI) with multi-omics in traditional Chinese medicine (TCM) through comprehensive bibliometric analysis.

Methods

China National Knowledge Infrastructure (CNKI), Wanfang Data, China Science and Technology Journal Database (VIP), Chaoxing Journal Database, PubMed, and Web of Science were searched to collect literature on the theme of AI in TCM multi-omics research from the inception of each database to December 31, 2024. Eligible records were required to simultaneously address AI, TCM, and multi-omics. Quantitative and visual analyses of publication growth, core authorship networks, institutional collaboration patterns, and keyword co-occurrence were performed using Microsoft Excel 2021, NoteExpress v4.0.0, and Cite Space 6.3.R1. AI application modes in TCM multi-omics research were also categorized and summarized.

Results

A total of 1 106 articles were enrolled (932 Chinese and 174 English). Publication output has increased continuously since 2010 and accelerated after 2016. Region-specific collaboration clusters were identified, dominated by Beijing University of Chinese Medicine, China Academy of Chinese Medical Sciences, Shanghai University of Traditional Chinese Medicine, and Nanjing University of Chinese Medicine. Keyword co-occurrence analysis revealed that current AI applications predominantly centered on metabolomics and algorithms such as cluster analysis and data mining. Research foci mainly ranked as follows: single herbs, herbal formulae, and disease-syndrome differentiation.

Conclusion

Machine learning methods are the predominant integrative modality of AI in the realm of TCM multi-omics research at present, utilized for processing omics data and uncovering latent patterns therein. The domain of TCM, in addition to investigating omics information procured through high-throughput technologies, also integrates data on traditional Chinese medicinal substances and clinical phenotypes, progressing towards joint analysis of multi-omics, high-dimensionality of data, and multi-modality of information. Deep learning approaches represent an emerging trend in the field.
目的通过综合文献计量分析,了解人工智能(AI)与中医多组学融合的研究热点、发展趋势及存在的挑战。方法检索中国知网(CNKI)、万方数据、中国科技期刊数据库(VIP)、超星期刊数据库、PubMed、Web of Science,收集各数据库自建库至2024年12月31日人工智能在中医多组学研究中的相关文献。符合条件的记录需要同时处理人工智能、中医和多组学。使用Microsoft Excel 2021、NoteExpress v4.0.0和Cite Space 6.3.R1对论文发表增长、核心作者网络、机构合作模式和关键词共现进行定量和可视化分析。对人工智能在中医多组学研究中的应用模式进行了分类和总结。结果共纳入文献1 106篇,其中中文文献932篇,英文文献174篇。2010年以来,出版物产量持续增长,2016年以后增速加快。区域协作集群以北京中医药大学、中国中医药科学院、上海中医药大学和南京中医药大学为主。关键词共现分析显示,目前的人工智能应用主要集中在代谢组学和聚类分析、数据挖掘等算法上。研究重点主要有:单药、方剂、病证辨证。结论机器学习方法是目前人工智能在中医多组学研究领域的主要整合方式,用于处理组学数据并揭示其中的潜在规律。中医药领域除了研究通过高通量技术获取的组学信息外,还整合了中药材和临床表型的数据,朝着多组学、数据高维、信息多模态的联合分析方向发展。深度学习方法代表了该领域的一个新兴趋势。
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引用次数: 0
In silico evaluation of hsa-miR-125a-5p and hsa-miR-125b-5p as potential biomarkers for monitoring acupuncture treatment in rheumatoid arthritis hsa-miR-125a-5p和hsa-miR-125b-5p作为监测针刺治疗类风湿关节炎的潜在生物标志物的计算机评价
Q3 Medicine Pub Date : 2025-09-01 DOI: 10.1016/j.dcmed.2025.09.011
Gabriela Adriana Martínez-Martínez , Xavier Anaya-Reza , Martha Alicia Ballinas-Verdugo , José Eduardo Justo-Frausto , Sergio Rafael Carrillo-Patiño , Juan Fernando Montes-García , Alejandra Isabel Ortega-Meléndez , Nubia Denise Nieto-Vargas , Rogelio Frank Jiménez-Ortega

Objective

To perform an in silico bioinformatics analysis to identify differentially expressed microRNAs (miRNAs) implicated in rheumatoid arthritis (RA) pathogenesis and evaluate their potential as biomarkers for assessing therapeutic efficacy and monitoring acupuncture treatment.

Methods

miRNA microarray data (CEL and TXT formats) were acquired from human and murine RA models, with the latter undergoing acupuncture treatment. Data were normalized using the robust multi-array average (RMA) method and analyzed for differential expression. Differential expression analysis identified miRNAs through a comparative analysis of RA human tissues, acupuncture-treated murine RA models, and a bibliographic search for miRNAs implicated in RA pathogenesis and acupuncture treatment. Bioinformatics analysis was performed to identify potential target genes for each miRNA and signaling pathways via search tools for the Retrieval of Interacting Genes/Proteins (STRING) and ShinyGO. Gene-drug interaction analysis was performed through Drug-Gene Interaction Database (DGIdb) screening. Interaction networks were constructed with the Cytoscape v3.10.3 software.

Results

The hsa-miR-125a-5p and hsa-miR-125b-5p were identified as potential biomarkers associated with RA pathogenesis, presenting 468 and 455 target genes, respectively. These genes were enriched in 20 signaling pathways, including Janus kinasa-signal transducer and activator of transcription (JAK-STAT), mitogen-activated protein kinase (MAPK), phosphoinositide 3-kinase-protein kinase B (PI3K-Akt), and nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) signaling pathway, which have been associated with RA pathogenesis and progression. Drug-gene interaction networks revealed that 22 genes were significantly associated with 58 RA treatment drugs, among which 13 genes interacted with members of the hsa-miR-125 family.

Conclusion

The hsa-miR-125a-5p and hsa-miR-125b-5p demonstrate critical regulatory role in RA pathogenesis by modulating signaling pathways, including JAK-STAT, MAPK, PI3K-Akt, and NF-κB. Our findings show that the hsa-miR-125a-5p and hsa-miR-125b-5p exhibit differential expression patterns in response to pharmacological intervention in various diseases, including RA management. This suggests their potential roles as biomarkers for monitoring acupuncture treatment. Although existing evidence indicates that acupuncture can modify miRNA expression profiles, rigorous validation through biological models remains essential to confirm these results.
目的通过计算机生物信息学分析,鉴定与类风湿关节炎(RA)发病机制有关的差异表达microRNAs (miRNAs),并评估其作为评估治疗效果和监测针灸治疗的生物标志物的潜力。方法对针刺治疗的人类RA模型和小鼠RA模型分别采集CEL和TXT格式的mirna微阵列数据。使用鲁棒多阵列平均(RMA)方法对数据进行归一化,并分析差分表达式。差异表达分析通过对RA人体组织与针灸治疗的小鼠RA模型的比较分析,以及对与RA发病机制和针灸治疗相关的mirna的文献检索来鉴定mirna。通过检索相互作用基因/蛋白(STRING)和ShinyGO的搜索工具进行生物信息学分析,以确定每个miRNA和信号通路的潜在靶基因。通过药物-基因相互作用数据库(DGIdb)筛选进行基因-药物相互作用分析。使用Cytoscape v3.10.3软件构建交互网络。结果hsa-miR-125a-5p和hsa-miR-125b-5p被鉴定为与RA发病机制相关的潜在生物标志物,分别有468个和455个靶基因。这些基因富集在20条信号通路中,包括与RA发病和进展相关的野蚕丝-信号传导和转录激活因子(JAK-STAT)、丝裂原活化蛋白激酶(MAPK)、磷酸肌苷3-激酶-蛋白激酶B (PI3K-Akt)和活化B细胞核因子κ轻链增强子(NF-κB)信号通路。药物-基因相互作用网络显示22个基因与58种RA治疗药物显著相关,其中13个基因与hsa-miR-125家族成员相互作用。结论hsa-miR-125a-5p和hsa-miR-125b-5p通过调控JAK-STAT、MAPK、PI3K-Akt、NF-κB等信号通路,在RA发病过程中发挥重要调控作用。我们的研究结果表明,hsa-miR-125a-5p和hsa-miR-125b-5p在包括RA管理在内的各种疾病的药物干预中表现出不同的表达模式。这表明它们作为监测针灸治疗的生物标志物的潜在作用。尽管现有证据表明针灸可以改变miRNA表达谱,但通过生物学模型进行严格验证仍然是确认这些结果的必要条件。
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引用次数: 0
Mechanism of electroacupuncture treating detrusor-bladder neck dyssynergia after suprasacral spinal cord injury by proteomics 电针治疗骶上脊髓损伤后逼尿肌-膀胱颈协同障碍的蛋白质组学机制
Q3 Medicine Pub Date : 2025-06-01 DOI: 10.1016/j.dcmed.2025.05.011
Liya Tang , Qirui Qu , Jincan Liu , Ming Xu , Lu Zhou , Qiong Liu , Kun Ai
<div><h3>Objectives</h3><div>To elucidate the potential mechanisms of electroacupuncture (EA) in restoring detrusor-bladder neck dyssynergia (DBND) following suprasacral spinal cord injury (SSCI).</div></div><div><h3>Methods</h3><div>A total of 52 specific pathogen-free (SPF) grade famale Sprague-Dawley (SD) rats (10 – 12 weeks, 250 – 280 g) were randomly assigned to either a sham group (<em>n</em> = 12) or a spinal cord injury model group (<em>n</em> = 40). In the model group, DBND was induced through Hassan Shaker spinal cord transection at T10 level, with 24 rats meeting inclusion criteria and subsequently randomized into DBND group (<em>n</em> = 12) and EA intervention group (DBND + EA group, <em>n</em> = 12). After spinal shock recovery (day 19 after modeling), DBND + EA group received EA treatment at Ciliao (BL32), Zhongji (RN3), and Sanyinjiao (SP6) acupoints for 20 min per session at 10/50 Hz frequencies, once daily for 10 d. Sham and DBND groups received anesthesia only without EA intervention. On day 29 post-modeling, all rats underwent urodynamic assessments, followed by hematoxylin and eosin (HE) staining, tandem mass tag (TMT) proteomics, and Western blot (WB) analysis of detrusor and bladder neck tissues. Differentially expressed proteins (DEPs) were defined as proteins with <em>P</em> < 0.05, unique peptides ≥ 2, and fold change > 1.2 or < 0.83. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis was performed using KOBAS 3.0 (<em>P</em> < 0.01), and protein-protein interaction (PPI) networks were analyzed using Search Tool for the Retrieval of Interacting Genes/Proteins (STRING) 11.5 and Cytoscape 3.9.1.</div></div><div><h3>Results</h3><div>Compared with sham group, DBND group showed significantly elevated leak point pressure (LPP) and maximum cystometric capacity (MCC) (both <em>P</em> < 0.01). EA treatment significantly reduced both LPP and MCC compared with DBND group (<em>P</em> < 0.01 and <em>P</em> < 0.05, respectively). HE staining revealed that EA reduced detrusor fibrosis and improved bladder neck inflammation. TMT proteomics identified 30 overlapping DEPs in detrusor and 59 overlapping DEPs in bladder neck when comparing DBND + EA/DBND groups with sham group. In detrusor tissue, KEGG analysis revealed 10 significantly enriched pathways (<em>P</em> < 0.01), including mitogen-activated protein kinase (MAPK) signaling pathway. PPI analysis showed 22 of 30 DEPs were interconnected. In bladder neck tissue, 14 pathways were significantly enriched (<em>P</em> < 0.01), including relaxin signaling pathway, with 51 of 59 DEPs showing interconnections. Both TMT and WB validations demonstrated that compared with sham controls, DBND rats exhibited upregulated collagen type IV alpha 2 chain (Col4a2) and downregulated guanine nucleotide-binding protein G(z) subunit alpha (Gnaz) in detrusor tissue, while EA treatment normalized both proteins (both <em>P</em> < 0.05). In bladder neck tissue, DBND
目的探讨电针(EA)治疗骶上脊髓损伤(SSCI)后逼尿肌-膀胱颈协同障碍(DBND)的可能机制。方法选取SPF级雌性SD大鼠52只(10 ~ 12周龄,250 ~ 280 g),随机分为假手术组(n = 12)和脊髓损伤模型组(n = 40)。模型组采用T10水平Hassan Shaker脊髓横断诱导DBND,符合纳入标准的24只大鼠随机分为DBND组(n = 12)和EA干预组(DBND + EA组,n = 12)。脊髓休克恢复后(造模后第19天),DBND + EA组在Ciliao (BL32)、Zhongji (RN3)、Sanyinjiao (SP6)穴位进行10/50 Hz频率的EA治疗,每次20 min,每日1次,连续10 d。Sham组和DBND组仅麻醉,不进行EA干预。造模后第29天,所有大鼠进行尿动力学评估,随后进行苏木精和伊红(HE)染色、tandem mass tag (TMT)蛋白质组学和逼尿肌和膀胱颈部组织的Western blot (WB)分析。差异表达蛋白(DEPs)被定义为含有P和lt的蛋白;0.05,独特肽≥2,折叠变化>;1.2或<;0.83. 京都基因与基因组百科全书(KEGG)通路分析采用KOBAS 3.0 (P <;使用Search Tool for Retrieval of Interacting Genes/Proteins (STRING) 11.5和Cytoscape 3.9.1分析蛋白质-蛋白质相互作用(PPI)网络。结果与假手术组比较,DBND组渗漏点压力(LPP)和最大膀胱容量(MCC)均显著升高(P <;0.01)。与DBND组相比,EA治疗显著降低LPP和MCC (P <;0.01和P <;分别为0.05)。HE染色显示,EA减轻了逼尿肌纤维化,改善了膀胱颈炎症。与假手术组比较,dnd + EA/DBND组在逼尿肌发现30个重叠dep,膀胱颈部发现59个重叠dep。在逼尿肌组织中,KEGG分析显示了10条显著富集的通路(P <;0.01),包括丝裂原活化蛋白激酶(MAPK)信号通路。PPI分析显示,30例dep中有22例相互关联。在膀胱颈部组织中,14条通路显著富集(P <;0.01),包括松弛素信号通路,59个dep中有51个显示相互连接。TMT和WB验证表明,与假对照组相比,DBND大鼠在逼尿肌组织中表现出ⅳ型胶原α 2链(Col4a2)上调和鸟嘌呤核苷酸结合蛋白G(z)亚基α (Gnaz)下调,而EA治疗使这两种蛋白(P <;0.05)。在膀胱颈部组织中,DBND大鼠与假对照组相比,平滑素(Smtn)和钙活化钾通道亚基β -1 (Kcnmb1)的表达降低(P <;0.01), EA治疗后两者均上调(P <;0.01和P <;分别为0.05)。结论ea通过双靶点机制恢复DBND患者逼尿肌-膀胱颈协调功能。在逼尿肌组织中,EA通过细胞外基质重塑、环磷酸腺苷(cAMP)信号通路调节和神经递质介导的三磷酸腺苷(ATP)生物合成增强来调节收缩。在膀胱颈部组织中,EA通过维持收缩表型、减少纤维化、抑制平滑肌兴奋和调节突触前神经递质释放来促进松弛。这些发现为EA在治疗DBND中的作用提供了机制上的见解。
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引用次数: 0
Correlation analysis between facial feature-based traditional Chinese medicine inspection of spirit classification and Beck Depression Inventory score 基于面相特征的中医精神分类检验与贝克抑郁量表评分的相关分析
Q3 Medicine Pub Date : 2025-06-01 DOI: 10.1016/j.dcmed.2025.06.002
Shan Lu , Xubo Shang , Dong Yang , Junfeng Yan , Xiaoye Wang

Objective

To determine the correlation between traditional Chinese medicine (TCM) inspection of spirit classification and the severity grade of depression based on facial features, offering insights for intelligent intergrated TCM and western medicine diagnosis of depression.

Methods

Using the Audio-Visual Emotion Challenge and Workshop (AVEC 2014) public dataset on depression, which conclude 150 interview videos, the samples were classified according to the TCM inspection of spirit classification: Deshen (得神, presence of spirit), Shaoshen (少神, insufficiency of spirit), and Shenluan (神乱, confusion of spirit). Meanwhile, based on Beck Depression Inventory-II (BDI-II) score for the severity grade of depression, the samples were divided into minimal (0 – 13, Q1), mild (14 – 19, Q2), moderate (20 – 28, Q3), and severe (29 – 63, Q4). Sixty-eight landmarks were extracted with a ResNet-50 network, and the feature extracion mode was stadardized. Random forest and support vectior machine (SVM) classifiers were used to predict TCM inspection of spirit classification and the severity grade of depression, respectively. A Chi-square test and Apriori association rule mining were then applied to quantify and explore the relationships.

Results

The analysis revealed a statistically significant and moderately strong association between TCM spirit classification and the severity grade of depression, as confirmed by a Chi-square test (χ2 = 14.04, P = 0.029) with a Cramer’s V effect size of 0.243. Further exploration using association rule mining identified the most compelling rule: “moderate depression (Q3) → Shenluan”. This rule demonstrated a support level of 5%, indicating this specific co-occurrence was present in 5% of the cohort. Crucially, it achieved a high Confidence of 86%, meaning that among patients diagnosed with Q3, 86% exhibited the Shenluan pattern according to TCM assessment. The substantial Lift of 2.37 signifies that the observed likelihood of Shenluan manifesting in Q3 patients is 2.37 times higher than would be expected by chance if these states were independent—compelling evidence of a highly non-random association. Consequently, Shenluan emerges as a distinct and core TCM diagnostic manifestation strongly linked to Q3, forming a clinically significant phenotype within this patient subgroup.

Conclusion

Automated facial analysis can serve as a common lens for TCM and western psychological assessments align in the diagnosis of depression. The inspection of spirit decline trajectory parallels worsening depression, supporting early screening and stratified intervention, and providing a reference for the intelligent assistance of integrated TCM and western medicine in the diagnosis of depression.
目的探讨基于面部特征的中医精神分型检查与抑郁症严重程度的相关性,为抑郁症的中西医结合智能诊断提供依据。方法利用AVEC 2014抑郁症视听情感挑战与研讨会(AVEC 2014)公开数据集(共150个访谈视频),将样本按照精神分类的中医检验进行分类:德神(精神存在)、少神(精神不足)和神乱(精神混乱)。同时,根据贝克抑郁量表- ii (BDI-II)抑郁严重程度评分,将样本分为轻度(0 - 13分,Q1)、轻度(14 - 19分,Q2)、中度(20 - 28分,Q3)和重度(29 - 63分,Q4)。采用ResNet-50网络提取68个地标,并对特征提取模式进行标准化。采用随机森林分类器和支持向量机分类器分别对精神分类和抑郁严重程度进行中医检验预测。然后应用卡方检验和Apriori关联规则挖掘来量化和探索关系。结果经卡方检验(χ2 = 14.04, P = 0.029), Cramer 's V效应值为0.243,中医精神分级与抑郁严重程度有统计学意义,相关性为中强。使用关联规则挖掘的进一步探索确定了最引人注目的规则:“中度抑郁(Q3)→深鸾”。该规则显示了5%的支持水平,表明5%的队列中存在这种特定的共发生。至关重要的是,它达到了86%的高置信度,这意味着在被诊断为Q3的患者中,86%的人根据中医评估表现出神鸾型。2.37的大幅提升表明,如果这些状态是高度非随机关联的独立有力证据,那么观察到的Q3患者出现神鸾的可能性是偶然预期的2.37倍。因此,神鸾成为与Q3密切相关的一种独特而核心的中医诊断表现,在该患者亚群中形成了具有临床意义的表型。结论面部自动分析可作为中医与西医心理评估相结合诊断抑郁症的通用视角。精神衰退轨迹检查与抑郁症加重平行,支持早期筛查和分层干预,为中西医结合诊断抑郁症的智能辅助提供参考。
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引用次数: 0
Lantana camara alleviating TNBS-induced ulcerative colitis in rats: regulating TNF-α/EGFR/STAT3/Bcl-2 signaling pathways 山楂缓解tnbs诱导的大鼠溃疡性结肠炎:调节TNF-α/EGFR/STAT3/Bcl-2信号通路
Q3 Medicine Pub Date : 2025-06-01 DOI: 10.1016/j.dcmed.2025.05.009
S. Magre Manoj, A. Bhalerao Pooja, K. Mandlik Satish, S. Mandlik Deepa

Objective

To investigate the therapeutic potential and underlying mechanism of Lantana camara ethanolic extract (LCEE) in ulcerative colitis (UC).

Methods

Phytochemical analysis of LCEE was conducted using qualitative analysis, liquid chromatography-mass spectrometry (LC-MS), and high-performance thin-layer chromatography (HPTLC). The active constituents of LCEE were identified through network pharmacology analysis, followed by molecular docking. The therapeutic mechanism was validated in a UC rat model using 42 male Wistar rats (200 – 250 g) induced by 2,4,6-trinitrobenzene sulfonic acid (TNBS). Rats were randomly divided into seven groups (n = 6 per group): normal control (NC), ethanol control (EC), disease control (DC), three doses of LCEE treatment [low dose LCEE (100 mg/kg), medium dose LCEE (200 mg/kg), and high dose LCEE (400 mg/kg), p.o.], and dexamethasone (DEX, 2 mg/kg, p.o.) groups. Following TNBS-induced UC (120 mg/kg, intrarectally), rats were treated orally for 28 d. Disease severity was assessed through body weight changes, disease activity index (DAI), colon weight, colon length, and morphological scores. Haematological parameters, enzymatic antioxidants, nitric oxide (NO), myeloperoxidase (MPO), and inflammatory cytokines were measured in the serum and colon tissues. Gene expressions of tumor necrosis factor (TNF)-α, epidermal growth factor receptor (EGFR), signal transducer and activator of transcription 3 (STAT3), and B-cell lymphoma 2 (Bcl-2) were analyzed by quantitative reverse transcription polymerase chain reaction (qRT-PCR). Histopathological alterations in the colon tissues were evaluated using hematoxylin and eosin (HE), Giemsa, and periodic acid-schiff staining (PAS).

Results

LC-MS analysis identified 13 phytoconstituents in LCEE, and HPTLC analysis confirmed the presence of ursolic acid, geniposide, and chlorogenic acid. Network pharmacological analysis identified 152 potential therapeutic targets with TNF, STAT3, Bcl-2, albumin (ALB), and EGFR as the top 5 hub targets. Molecular docking revealed strong binding affinities of LCEE phytoconstituents with key inflammatory and apoptotic targets: linaroside with TNF-α (– 6.1 kcal/mol), ursolic acid with STAT3 (– 6.8 kcal/mol) and Bcl-2 (– 8.7 kcal/mol), and cirsiliol with EGFR (– 8.2 kcal/mol), comparable to DEX. LCEE treatment significantly increased body weights and thymus weight, while significantly reducing colon weight, spleen weight, and DAI scores. Haematological parameters showed significant improvements with increased haemoglobin, red blood cells, and platelet count, and decreased white blood cells counts. Antioxidants markers were significantly improved with increased glutathione, superoxide dismutase, and catalase levels, and decreased malondialdehyde levels. LCEE significantly reduced NO and MPO levels and inflammatory cytokines including TNF-α, interleukin (IL)-1β, nu
目的探讨枸杞子乙醇提取物(LCEE)对溃疡性结肠炎(UC)的治疗作用及其机制。方法采用定性分析、液相色谱-质谱联用(LC-MS)和高效薄层色谱(HPTLC)对LCEE进行植物化学分析。通过网络药理学分析鉴定出LCEE的有效成分,并进行分子对接。采用2,4,6-三硝基苯磺酸(TNBS)诱导的42只雄性Wistar大鼠(200 ~ 250 g)建立UC大鼠模型,验证其治疗机制。将大鼠随机分为7组(每组n = 6):正常对照组(NC)、乙醇对照组(EC)、疾病对照组(DC)、LCEE低剂量(100 mg/kg)、中剂量(200 mg/kg)、高剂量(400 mg/kg)、地塞米松组(DEX, 2 mg/kg, p / o)。在tnbs诱导UC (120 mg/kg,直肠内注射)后,大鼠口服治疗28 d。通过体重变化、疾病活动指数(DAI)、结肠重量、结肠长度和形态学评分评估疾病严重程度。测定血清和结肠组织中的血液学参数、酶促抗氧化剂、一氧化氮(NO)、髓过氧化物酶(MPO)和炎性细胞因子。采用定量逆转录聚合酶链式反应(qRT-PCR)分析肿瘤坏死因子(TNF)-α、表皮生长因子受体(EGFR)、转录信号传导和激活因子3 (STAT3)、b细胞淋巴瘤2 (Bcl-2)的基因表达。采用苏木精和伊红染色(HE)、吉姆萨染色和周期性酸希夫染色(PAS)评估结肠组织的组织病理学改变。结果薄层色谱-质谱分析鉴定出13种植物成分,HPTLC分析鉴定出熊果酸、京尼平苷和绿原酸。网络药理学分析确定了152个潜在的治疗靶点,其中TNF、STAT3、Bcl-2、白蛋白(ALB)和EGFR是前5个中心靶点。分子对接显示,LCEE植物成分与关键的炎症和凋亡靶点有很强的结合亲和力:linar苷与TNF-α (- 6.1 kcal/mol),熊果酸与STAT3 (- 6.8 kcal/mol)和Bcl-2 (- 8.7 kcal/mol),千里油与EGFR (- 8.2 kcal/mol),与DEX相当。LCEE治疗显著增加了体重和胸腺重量,同时显著降低了结肠重量、脾脏重量和DAI评分。血液学参数随着血红蛋白、红细胞和血小板计数的增加和白细胞计数的减少而显著改善。抗氧化指标随着谷胱甘肽、超氧化物歧化酶和过氧化氢酶水平的升高和丙二醛水平的降低而显著改善。与TNBS处理的大鼠相比,LCEE显著降低NO和MPO水平以及炎症因子TNF-α、白细胞介素(IL)-1β、核因子κ b (NF-κB)、IL-6和IL-12。LCEE下调TNF-α、EGFR和STAT3基因表达水平,上调Bcl-2基因表达水平,提示炎症和凋亡通路的调节。组织学评价证实,经LECC治疗后,粘膜溃疡和炎症细胞浸润减少。结论大戟属植物可作为缓解UC的药用植物,为大戟属植物的临床应用提供了研究依据。
{"title":"Lantana camara alleviating TNBS-induced ulcerative colitis in rats: regulating TNF-α/EGFR/STAT3/Bcl-2 signaling pathways","authors":"S. Magre Manoj,&nbsp;A. Bhalerao Pooja,&nbsp;K. Mandlik Satish,&nbsp;S. Mandlik Deepa","doi":"10.1016/j.dcmed.2025.05.009","DOIUrl":"10.1016/j.dcmed.2025.05.009","url":null,"abstract":"<div><h3>Objective</h3><div>To investigate the therapeutic potential and underlying mechanism of <em>Lantana camara</em> ethanolic extract (LCEE) in ulcerative colitis (UC).</div></div><div><h3>Methods</h3><div>Phytochemical analysis of LCEE was conducted using qualitative analysis, liquid chromatography-mass spectrometry (LC-MS), and high-performance thin-layer chromatography (HPTLC). The active constituents of LCEE were identified through network pharmacology analysis, followed by molecular docking. The therapeutic mechanism was validated in a UC rat model using 42 male Wistar rats (200 – 250 g) induced by 2,4,6-trinitrobenzene sulfonic acid (TNBS). Rats were randomly divided into seven groups (<em>n</em> = 6 per group): normal control (NC), ethanol control (EC), disease control (DC), three doses of LCEE treatment [low dose LCEE (100 mg/kg), medium dose LCEE (200 mg/kg), and high dose LCEE (400 mg/kg), p.o.], and dexamethasone (DEX, 2 mg/kg, p.o.) groups. Following TNBS-induced UC (120 mg/kg, intrarectally), rats were treated orally for 28 d. Disease severity was assessed through body weight changes, disease activity index (DAI), colon weight, colon length, and morphological scores. Haematological parameters, enzymatic antioxidants, nitric oxide (NO), myeloperoxidase (MPO), and inflammatory cytokines were measured in the serum and colon tissues. Gene expressions of tumor necrosis factor (TNF)-α, epidermal growth factor receptor (EGFR), signal transducer and activator of transcription 3 (STAT3), and B-cell lymphoma 2 (Bcl-2) were analyzed by quantitative reverse transcription polymerase chain reaction (qRT-PCR). Histopathological alterations in the colon tissues were evaluated using hematoxylin and eosin (HE), Giemsa, and periodic acid-schiff staining (PAS).</div></div><div><h3>Results</h3><div>LC-MS analysis identified 13 phytoconstituents in LCEE, and HPTLC analysis confirmed the presence of ursolic acid, geniposide, and chlorogenic acid. Network pharmacological analysis identified 152 potential therapeutic targets with TNF, STAT3, Bcl-2, albumin (ALB), and EGFR as the top 5 hub targets. Molecular docking revealed strong binding affinities of LCEE phytoconstituents with key inflammatory and apoptotic targets: linaroside with TNF-α (– 6.1 kcal/mol), ursolic acid with STAT3 (– 6.8 kcal/mol) and Bcl-2 (– 8.7 kcal/mol), and cirsiliol with EGFR (– 8.2 kcal/mol), comparable to DEX. LCEE treatment significantly increased body weights and thymus weight, while significantly reducing colon weight, spleen weight, and DAI scores. Haematological parameters showed significant improvements with increased haemoglobin, red blood cells, and platelet count, and decreased white blood cells counts. Antioxidants markers were significantly improved with increased glutathione, superoxide dismutase, and catalase levels, and decreased malondialdehyde levels. LCEE significantly reduced NO and MPO levels and inflammatory cytokines including TNF-α, interleukin (IL)-1β, nu","PeriodicalId":33578,"journal":{"name":"Digital Chinese Medicine","volume":"8 2","pages":"Pages 234-253"},"PeriodicalIF":0.0,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144772474","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
Construction and evaluation of a predictive model for the degree of coronary artery occlusion based on adaptive weighted multi-modal fusion of traditional Chinese and western medicine data 基于中西医数据自适应加权多模态融合的冠状动脉闭塞程度预测模型的构建与评价
Q3 Medicine Pub Date : 2025-06-01 DOI: 10.1016/j.dcmed.2025.05.005
Jiyu ZHANG, Jiatuo XU, Liping TU, Hongyuan FU

Objective

To develop a non-invasive predictive model for coronary artery stenosis severity based on adaptive multi-modal integration of traditional Chinese and western medicine data.

Methods

Clinical indicators, echocardiographic data, traditional Chinese medicine (TCM) tongue manifestations, and facial features were collected from patients who underwent coronary computed tomography angiography (CTA) in the Cardiac Care Unit (CCU) of Shanghai Tenth People's Hospital between May 1, 2023 and May 1, 2024. An adaptive weighted multi-modal data fusion (AWMDF) model based on deep learning was constructed to predict the severity of coronary artery stenosis. The model was evaluated using metrics including accuracy, precision, recall, F1 score, and the area under the receiver operating characteristic (ROC) curve (AUC). Further performance assessment was conducted through comparisons with six ensemble machine learning methods, data ablation, model component ablation, and various decision-level fusion strategies.

Results

A total of 158 patients were included in the study. The AWMDF model achieved excellent predictive performance (AUC = 0.973, accuracy = 0.937, precision = 0.937, recall = 0.929, and F1 score = 0.933). Compared with model ablation, data ablation experiments, and various traditional machine learning models, the AWMDF model demonstrated superior performance. Moreover, the adaptive weighting strategy outperformed alternative approaches, including simple weighting, averaging, voting, and fixed-weight schemes.

Conclusion

The AWMDF model demonstrates potential clinical value in the non-invasive prediction of coronary artery disease and could serve as a tool for clinical decision support.
目的建立一种基于中西医数据自适应多模式整合的冠状动脉狭窄程度无创预测模型。方法收集2023年5月1日至2024年5月1日在上海市第十人民医院心内科(CCU)行冠状动脉ct血管造影(CTA)的患者的临床指标、超声心动图资料、中医舌部表现及面部特征。构建基于深度学习的自适应加权多模态数据融合(AWMDF)模型预测冠状动脉狭窄严重程度。采用准确度、精密度、召回率、F1评分和受试者工作特征曲线下面积(AUC)等指标对模型进行评价。通过比较六种集成机器学习方法、数据消融、模型成分消融和各种决策级融合策略,进一步进行性能评估。结果共纳入158例患者。AWMDF模型取得了较好的预测效果(AUC = 0.973,准确率= 0.937,精密度= 0.937,召回率= 0.929,F1得分= 0.933)。与模型烧蚀、数据烧蚀实验以及各种传统机器学习模型相比,AWMDF模型表现出了优越的性能。此外,自适应加权策略优于其他方法,包括简单加权、平均、投票和固定权重方案。结论AWMDF模型在无创预测冠状动脉疾病方面具有潜在的临床价值,可作为临床决策支持工具。
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引用次数: 0
Herbal remedies for Alzheimer’s disease: neuroprotective mechanisms and cognitive enhancement potential 阿尔茨海默病的草药疗法:神经保护机制和认知增强潜力
Q3 Medicine Pub Date : 2025-06-01 DOI: 10.1016/j.dcmed.2025.05.002
Dharmalingam Kirubakaran
Alzheimer’s disease (AD) is a progressive neurodegenerative condition characterized by memory loss and cognitive decline. Current drugs offer limited benefits and often cause side effects. Recently, interest has grown in medicinal plants for the treatment of AD due to their neuroprotective compounds. This review explores how herbal remedies may help AD, focusing on key plants including Ginkgo biloba, Curcuma longa, Withania somnifera, and Panax ginseng. These plants show promise in reducing inflammation, oxidative stress, and amyloid buildup. Their bioactive compounds, including flavonoids and alkaloids, may promote memory and slow AD progression. Despite these promising findings, the review also highlights significant challenges in translating preclinical success into clinical efficacy. Issues such as variability in plant composition, lack of standardized formulations, insufficient large-scale clinical trials, and regulatory hurdles continue to impede the integration of herbal therapies into mainstream AD treatment. Addressing these challenges through rigorous scientific validation and standardized protocols is essential for advancing the use of herbal medicine in neurodegenerative disease management.
阿尔茨海默病(AD)是一种以记忆丧失和认知能力下降为特征的进行性神经退行性疾病。目前的药物疗效有限,而且往往会产生副作用。近年来,由于药用植物具有神经保护作用,人们对治疗阿尔茨海默病的兴趣日益浓厚。这篇综述探讨了草药是如何帮助AD的,重点是包括银杏、姜黄、Withania somnifera和人参在内的关键植物。这些植物有望减少炎症、氧化应激和淀粉样蛋白的积累。它们的生物活性成分,包括类黄酮和生物碱,可以促进记忆和减缓AD的进展。尽管有这些有希望的发现,该综述也强调了将临床前成功转化为临床疗效的重大挑战。诸如植物成分的差异、缺乏标准化配方、大规模临床试验不足以及监管障碍等问题继续阻碍草药疗法融入主流AD治疗。通过严格的科学验证和标准化的方案来解决这些挑战,对于促进草药在神经退行性疾病管理中的应用至关重要。
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引用次数: 0
Clinical research report on Chinese patent medicines and classic traditional Chinese medicine prescriptions (2023) 中成药与中药经典方剂临床研究报告(2023年)
Q3 Medicine Pub Date : 2025-06-01 DOI: 10.1016/j.dcmed.2025.06.001
Xiaolei Wu , Haiyin Hu , Yuetong Wang , Alice Josephine Fauci , Yazi Zhang , Wenting Song , Fengwen Yang , Boli Zhang , Junhua Zhang , Zhaochen Ji

Objective

Randomized controlled trials (RCTs) of Chinese patent medicines and classic traditional Chinese medicine prescriptions were systematically reviewed from both Chinese and English journals published in 2023. A preliminary summary and evaluation were conducted on the generation and translation of clinical evidence for these treatments. This analysis aims to inform future research on clinical efficacy evaluation and guide the rational application of evidence.

Methods

RCTs of Chinese patent medicines and classic traditional Chinese prescriptions published in 2023 were comprehensively retrieved from the Artificial Intelligence Clinical Evidence Database for Chinese Patent Medicine (AICED-CPM), with supplementary searches conducted in China National Knowledge Infrastructure (CNKI), Wanfang Data, Chinese Science and Technology Journal Database (VIP), Chinese Biomedical Literature Database (SinoMed), Cochrane Library, PubMed, Embase, and Web of Science. The study characteristics and methodological quality of these RCTs were systematically analyzed and evaluated.

Results

A total of 1 443 RCTs of Chinese patent medicines were included, comprising 1 399 Chinese articles and 44 English articles. Additionally, 334 RCTs of classic traditional Chinese medicine prescriptions were found, with 331 published in Chinese and 3 in English. 196 567 participants were included, covering 585 types of Chinese patent medicines (487 oral, 61 injectable, and 37 topical) and 179 classic traditional Chinese medicine prescriptions. The involved studies encompassed 22 types of diseases, with research primarily focusing on diseases of the circulatory system, the respiratory system, and the genitourinary system. The sample sizes ranged from 18 to 3 777 participants, and most studies were conducted at a single center. Methodologically, the implementation of allocation concealment and blinding remained insufficiently emphasized.

Conclusion

Overall, compared with 2022, both the number of RCT publications and their methodological quality have improved in 2023, with heightened attention to research on diseases of the genitourinary system. However, quality control and standardized management in the design and implementation processes still require enhancement to produce more high-quality clinical evidence and accelerate the translation and application of this evidence.
目的对2023年发表的中英文期刊中成药和中药经典方剂的随机对照试验(rct)进行系统回顾。对这些治疗的临床证据的生成和转化进行了初步的总结和评价。本分析旨在为今后临床疗效评价的研究提供参考,指导证据的合理应用。方法综合检索中国中成药人工智能临床证据数据库(AICED-CPM)中2023年发表的中成药和中药经典方剂的srct,并辅以中国知网(CNKI)、万方数据、中国科技期刊数据库(VIP)、中国生物医学文献数据库(SinoMed)、Cochrane图书馆、PubMed、Embase和Web of Science。对这些随机对照试验的研究特点和方法学质量进行系统分析和评价。结果共纳入中成药rct 1 443篇,其中中文文献1 399篇,英文文献44篇。共纳入中药经典方剂rct 334项,其中中文发表方剂331项,英文发表方剂3项,共纳入受试者19567人,涵盖585种中成药(口服487种,注射61种,外用37种)和179种中药经典方剂。所涉及的研究包括22种疾病,研究主要集中在循环系统、呼吸系统和泌尿生殖系统的疾病。样本量从18到3777人不等,大多数研究在单一中心进行。在方法上,分配隐瞒和盲法的实施仍然不够强调。结论总体而言,与2022年相比,2023年的RCT出版物数量和方法学质量均有所提高,对泌尿生殖系统疾病研究的重视程度有所提高。然而,在设计和实施过程中,仍需加强质量控制和规范管理,以产生更多高质量的临床证据,加快临床证据的转化和应用。
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引用次数: 0
Integrated plasma and synovial membrane lipidomic profiling revealing the therapeutic effects of moxibustion in collagen-induced arthritis rat models 血浆和滑膜脂质组学分析揭示艾灸对胶原性关节炎大鼠模型的治疗作用
Q3 Medicine Pub Date : 2025-06-01 DOI: 10.1016/j.dcmed.2025.05.010
Jiamin Wen , Rui Zhang , Danwen Wang , Zhiling Sun
<div><h3>Objective</h3><div>To reveal the therapeutic effects of moxibustion in collagen-induced arthritis (CIA) rat models using the combined analysis of plasma and synovial membrane lipidomic profiling and to enhance the understanding of how moxibustion affects lipid metabolism in rheumatoid arthritis (RA).</div></div><div><h3>Methods</h3><div>A total of 32 male Sprague-Dawley (SD) rats were randomly assigned to four groups: control, moxibustion control (MC), model, and moxibustion model (MM) groups, with 8 rats in each group. CIA was induced in SD rats by two immunizations. The paw volume was measured before the induction of CIA. Following induction, after assessing paw volume and arthritis index (AI) scores, the MC and MM groups received treatment at bilateral Shenshu (BL23) and Zusanli (ST36) acupoints for 10 min per acupoint. The intervention included three treatment courses, each spanning 6 d and followed by a 1-d interval. Paw volume and AI scores were assessed after each treatment course. After the completion of the three treatment courses, serum, plasma, synovial tissue, and ankle joint samples were collected. Enzyme-linked immunosorbent assay (ELISA) was employed to quantify the levels of interleukin (IL)-6 and tumor necrosis factor (TNF)-α in serum. Hematoxylin and eosin (HE) staining was performed for histopathological examination of the ankle joint tissues. Meanwhile, ultra-high-performance liquid chromatography coupled with Q-Exactive Orbitrap mass spectrometry (UHPLC-Q-Exactive Orbitrap MS) was utilized to analyze the plasma and synovial tissue samples. In addition, multivariate statistical analysis was performed to identify differential lipid metabolites, and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis was applied to explore metabolic pathways modulated by moxibustion therapy.</div></div><div><h3>Results</h3><div>No significant difference in hind paw volume and AI scores was observed among the groups (<em>P</em> > 0.05). After CIA induction, model group showed increased hind paw volume and AI scores compared with control group (<em>P</em> < 0.05), which were significantly reduced after moxibustion treatment in MM group compared with model group (<em>P</em> < 0.05). The levels of IL-6 and TNF-α were significantly higher in model and MM groups compared with control group (<em>P</em> < 0.05), but were lower in MM group than those in model group (<em>P</em> < 0.05). Histopathological analysis showed improved cartilage and reduced inflammation in MM group. A total of 33 differential lipid metabolites in the plasma and 24 in the synovial membranes of CIA rat models were identified when compared with control group. Among these lipid metabolites, 31 in the plasma and all 24 in the synovial membranes were regulated by moxibustion treatment. Pathological analysis revealed upregulation of diacylglycerol (DG) and fatty acid (FA) levels, alongside downregulation of lysophosphatidylcholine (LPC), p
目的通过血浆和滑膜脂质组学分析,探讨艾灸对类风湿关节炎(RA)大鼠模型的治疗作用,进一步了解艾灸对类风湿关节炎(RA)脂质代谢的影响。方法将32只雄性SD大鼠随机分为对照组、艾灸对照组、模型组和艾灸模型组,每组8只。SD大鼠通过两次免疫诱导CIA。CIA诱导前测定大鼠爪体积。诱导后,评估足爪体积和关节炎指数(AI)评分后,MC组和MM组分别在双侧肾俞穴(BL23)和足三里穴(ST36)治疗,每个穴治疗10 min。干预包括三个疗程,每个疗程跨越6天,随后是1天的间隔。每个疗程结束后评估爪体积和人工智能评分。三个疗程结束后,采集血清、血浆、滑膜组织及踝关节标本。采用酶联免疫吸附法(ELISA)测定血清中白细胞介素(IL)-6和肿瘤坏死因子(TNF)-α的水平。采用苏木精伊红(HE)染色对踝关节组织进行组织病理学检查。同时,采用超高效液相色谱-Q-Exactive Orbitrap质谱联用(UHPLC-Q-Exactive Orbitrap MS)对血浆和滑膜组织样品进行分析。此外,采用多变量统计分析鉴定差异脂质代谢物,并采用京都基因基因组百科全书(KEGG)途径富集分析探索艾灸疗法调节的代谢途径。结果各组大鼠后爪体积、AI评分差异无统计学意义(P >;0.05)。CIA诱导后,模型组大鼠后爪体积和AI评分均较对照组增加(P <;0.05),灸疗后MM组与模型组比较差异有统计学意义(P <;0.05)。模型组和MM组大鼠血清IL-6、TNF-α水平均显著高于对照组(P <;0.05), MM组低于模型组(P <;0.05)。组织病理学分析显示,MM组软骨改善,炎症减轻。与对照组相比,CIA大鼠模型血浆中鉴定出33种不同的脂质代谢物,滑膜中鉴定出24种不同的脂质代谢物。其中,血浆中的31种脂质代谢物和滑膜中的24种脂质代谢物均受艾灸治疗的调节。病理分析显示二酰基甘油(DG)和脂肪酸(FA)水平上调,同时溶磷脂酰胆碱(LPC)、磷脂酰胆碱(PC)和磷脂酰乙醇胺(PE)水平下调。生理条件下,处理能显著降低LPC和PC水平。途径富集分析显示,在病理条件下,艾灸主要影响α-亚麻酸、甘油磷脂和鞘脂代谢。生理条件下,调节主要围绕α-亚麻酸和甘油磷脂代谢进行。结论RA大鼠模型存在明显的脂质代谢紊乱。艾灸可减轻足跖肿胀,降低AI评分,调节炎症细胞因子水平,部分纠正多种脂质代谢物水平的改变。在生理和病理条件下,参与脂质代谢调节的潜在代谢途径包括α-亚麻酸、甘油磷脂和鞘脂代谢。
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Digital Chinese Medicine
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