{"title":"解码巴伯根的治疗网络:IBS-D的协同解决方案。","authors":"Qi Yan, Xufei Wang, Huijiao Jiang, Xuan Zhou, Xiangwei Wu, Xueling Chen","doi":"10.2174/0113862073421977250903053304","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Barberry Root (Sankezhen, SKZ), a traditional Uyghur herb from Xinjiang, China, has been shown to alleviate diarrhea-predominant irritable bowel syndrome (IBSD); however, its molecular mechanisms remain unclear. This study aimed to systematically predict SKZ's therapeutic targets and pathways for IBS-D using computational and experimental integration.</p><p><strong>Methods: </strong>Active SKZ compounds and targets were sourced from TCM-Suite, BATMAN-TCM, and related databases. IBS-D targets were identified via DisGeNET and GeneCards, etc. Protein- Protein Interaction (PPI) networks, Gene Ontology (GO), and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses were performed. Molecular docking and 100-ns Molecular Dynamics (MD) simulations validated compound-target stability. In vitro (LPS-induced RAW264.7 macrophages) and in vivo (IBS-D model rats, isolated intestinal segments) experiments verified SKZ's effects.</p><p><strong>Results: </strong>Fifteen bioactive compounds and 85 overlapping targets were identified, with four key compounds [(R)-Reticuline, Ferulic acid 4-O-glucoside, Magnoflorine, SW 7] and 15 hub targets (e.g., ESR1, EGF, ALB) prioritized. Enrichment analyses linked targets to inflammation and intestinal motility pathways. Docking showed strong binding affinities (<-8.0 kcal/mol), and MD simulations confirmed stability. SKZ suppressed inflammatory mediators, downregulated CHAT/C-FOS/5-HT3R/5-HT4R mRNA, and antagonized acetylcholine/barium chloride-induced intestinal contractions.</p><p><strong>Discussion: </strong>The findings highlight SKZ's synergistic role in ameliorating IBS-D via multipathway regulation, consistent with existing research on inflammation and neurotransmission, though limitations include the need for further validation of individual compounds.</p><p><strong>Conclusion: </strong>SKZ exerts synergistic therapeutic effects on IBS-D by ameliorating inflammation and regulating neurotransmission and intestinal motility, potentially via NF-κB/MAPK, COX- 2/PGE2, cholinergic/5-HT, and calcium/potassium channel pathways, forming a multidimensional network.</p>","PeriodicalId":10491,"journal":{"name":"Combinatorial chemistry & high throughput screening","volume":" ","pages":""},"PeriodicalIF":1.7000,"publicationDate":"2025-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Decoding Barberry Root's Therapeutic Network: A Synergistic Solution for IBS-D.\",\"authors\":\"Qi Yan, Xufei Wang, Huijiao Jiang, Xuan Zhou, Xiangwei Wu, Xueling Chen\",\"doi\":\"10.2174/0113862073421977250903053304\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Barberry Root (Sankezhen, SKZ), a traditional Uyghur herb from Xinjiang, China, has been shown to alleviate diarrhea-predominant irritable bowel syndrome (IBSD); however, its molecular mechanisms remain unclear. This study aimed to systematically predict SKZ's therapeutic targets and pathways for IBS-D using computational and experimental integration.</p><p><strong>Methods: </strong>Active SKZ compounds and targets were sourced from TCM-Suite, BATMAN-TCM, and related databases. IBS-D targets were identified via DisGeNET and GeneCards, etc. Protein- Protein Interaction (PPI) networks, Gene Ontology (GO), and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses were performed. Molecular docking and 100-ns Molecular Dynamics (MD) simulations validated compound-target stability. In vitro (LPS-induced RAW264.7 macrophages) and in vivo (IBS-D model rats, isolated intestinal segments) experiments verified SKZ's effects.</p><p><strong>Results: </strong>Fifteen bioactive compounds and 85 overlapping targets were identified, with four key compounds [(R)-Reticuline, Ferulic acid 4-O-glucoside, Magnoflorine, SW 7] and 15 hub targets (e.g., ESR1, EGF, ALB) prioritized. Enrichment analyses linked targets to inflammation and intestinal motility pathways. Docking showed strong binding affinities (<-8.0 kcal/mol), and MD simulations confirmed stability. 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引用次数: 0
摘要
杨梅根(Sankezhen, SKZ)是一种来自中国新疆的维吾尔族传统草药,已被证明可以缓解腹泻型肠易激综合征(IBSD);然而,其分子机制尚不清楚。本研究旨在通过计算和实验相结合的方法,系统预测SKZ对IBS-D的治疗靶点和通路。方法:活性SKZ化合物和靶点来源于TCM-Suite、BATMAN-TCM及相关数据库。通过DisGeNET和GeneCards等方法确定IBS-D靶点。进行了蛋白质-蛋白质相互作用(PPI)网络、基因本体(GO)和京都基因与基因组百科全书(KEGG)分析。分子对接和100-ns分子动力学(MD)模拟验证了化合物-靶标的稳定性。体外(lps诱导的RAW264.7巨噬细胞)和体内(IBS-D模型大鼠,离体肠段)实验验证了SKZ的作用。结果:共鉴定出15个生物活性化合物和85个重叠靶点,其中4个关键化合物[(R)-Reticuline,阿威酸4-O-glucoside, magnnoflorine, sw7]和15个枢纽靶点(如ESR1, EGF, ALB)优先。富集分析将靶标与炎症和肠道运动途径联系起来。对接显示出很强的结合亲和力(讨论:研究结果强调SKZ通过多途径调节改善IBS-D的协同作用,与现有的炎症和神经传递研究一致,尽管局限性包括需要进一步验证单个化合物。结论:SKZ可能通过NF-κ b /MAPK、COX- 2/PGE2、胆碱能/5-HT和钙/钾通道通路,形成一个多维网络,通过改善炎症、调节神经传递和肠道蠕动,对IBS-D具有协同治疗作用。
Decoding Barberry Root's Therapeutic Network: A Synergistic Solution for IBS-D.
Introduction: Barberry Root (Sankezhen, SKZ), a traditional Uyghur herb from Xinjiang, China, has been shown to alleviate diarrhea-predominant irritable bowel syndrome (IBSD); however, its molecular mechanisms remain unclear. This study aimed to systematically predict SKZ's therapeutic targets and pathways for IBS-D using computational and experimental integration.
Methods: Active SKZ compounds and targets were sourced from TCM-Suite, BATMAN-TCM, and related databases. IBS-D targets were identified via DisGeNET and GeneCards, etc. Protein- Protein Interaction (PPI) networks, Gene Ontology (GO), and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses were performed. Molecular docking and 100-ns Molecular Dynamics (MD) simulations validated compound-target stability. In vitro (LPS-induced RAW264.7 macrophages) and in vivo (IBS-D model rats, isolated intestinal segments) experiments verified SKZ's effects.
Results: Fifteen bioactive compounds and 85 overlapping targets were identified, with four key compounds [(R)-Reticuline, Ferulic acid 4-O-glucoside, Magnoflorine, SW 7] and 15 hub targets (e.g., ESR1, EGF, ALB) prioritized. Enrichment analyses linked targets to inflammation and intestinal motility pathways. Docking showed strong binding affinities (<-8.0 kcal/mol), and MD simulations confirmed stability. SKZ suppressed inflammatory mediators, downregulated CHAT/C-FOS/5-HT3R/5-HT4R mRNA, and antagonized acetylcholine/barium chloride-induced intestinal contractions.
Discussion: The findings highlight SKZ's synergistic role in ameliorating IBS-D via multipathway regulation, consistent with existing research on inflammation and neurotransmission, though limitations include the need for further validation of individual compounds.
Conclusion: SKZ exerts synergistic therapeutic effects on IBS-D by ameliorating inflammation and regulating neurotransmission and intestinal motility, potentially via NF-κB/MAPK, COX- 2/PGE2, cholinergic/5-HT, and calcium/potassium channel pathways, forming a multidimensional network.
期刊介绍:
Combinatorial Chemistry & High Throughput Screening (CCHTS) publishes full length original research articles and reviews/mini-reviews dealing with various topics related to chemical biology (High Throughput Screening, Combinatorial Chemistry, Chemoinformatics, Laboratory Automation and Compound management) in advancing drug discovery research. Original research articles and reviews in the following areas are of special interest to the readers of this journal:
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