An herbal formula alleviates hyperuricemia: Evidence from network pharmacology and in vivo experiments.

IF 1.7 4区 医学 Q4 BIOCHEMICAL RESEARCH METHODS
Luyin Yang, Zhihao Wu, Hai Du, Gang Luo, Raoqiong Wang, Wei Ren, Houping Xu
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引用次数: 0

Abstract

Qianhua Tongfeng Capsule (QHTFC), an herbal formula, has demonstrated favorable therapeutic efficacy in the clinical management of hyperuricemia (HUA) and gout. Phytochemical analysis revealed that QHTFC is primarily composed of coumarins, flavonoids, and alkaloids. Nevertheless, the anti-hyperuricemic mechanisms of QHTFC remain to be further elucidated. This study aimed to elucidate the molecular targets and potential mechanisms of QHTFC in the treatment of hyperuricemia (HUA) by combining network pharmacology with in vivo experimental validation. Network pharmacology was employed to predict the potential targets and signaling pathways of QHTFC against HUA. Subsequently, in vivo experiments were conducted to evaluate the effects of QHTFC on serum biochemical markers, oxidative stress indices, and renal histopathological changes in HUA rats. Moreover, the expression levels of uric acid transporter-related proteins in the kidney were analyzed using Western blotting to further validate the underlying mechanisms. Based on network pharmacology analysis, 57 intersecting targets between QHTFC and HUA were identified. Among them, IL-6, TNF, PPARγ, CXCL8, PTGS2, and ABCG2 were determined as key targets. KEGG enrichment analysis further indicated that the primary therapeutic pathway of QHTFC against HUA involved the IL-17 signaling pathway. In vivo results revealed that QHTFC exerted potent uric acid-lowering efficacy in hyperuricemic models by bidirectional modulation of uric acid transporters. Mechanistically, QHTFC suppressed liver XOD activity, thereby reducing uric acid production. Additionally, it promoted uric acid excretion both by upregulating OAT1 and ABCG2 transporters and suppressing reabsorption through the downregulation of GLUT9 and URAT1 expression. Our findings suggest that QHTFC can significantly reduce serum UA levels and ameliorate renal injury by regulating oxidative stress, inflammation, and kidney fibrosis. This research provides new evidence supporting the application of QHTFC in the treatment of hyperuricemia.

一种减轻高尿酸血症的草药配方:来自网络药理学和体内实验的证据。
千花痛风胶囊是一种中药方剂,在临床上治疗高尿酸血症(HUA)和痛风有良好的疗效。植物化学分析表明,QHTFC主要由香豆素、类黄酮和生物碱组成。然而,QHTFC抗高尿酸血症的机制仍有待进一步阐明。本研究旨在通过网络药理学和体内实验验证相结合,阐明QHTFC治疗高尿酸血症(HUA)的分子靶点和潜在机制。应用网络药理学方法预测了QHTFC抗HUA的潜在靶点和信号通路。随后,我们通过体内实验,评估了QHTFC对HUA大鼠血清生化指标、氧化应激指标和肾脏组织病理学变化的影响。此外,使用Western blotting分析肾脏中尿酸转运蛋白相关蛋白的表达水平,以进一步验证其潜在机制。基于网络药理学分析,确定了57个QHTFC和HUA之间的交叉靶点。其中IL-6、TNF、PPARγ、CXCL8、PTGS2、ABCG2被确定为关键靶点。KEGG富集分析进一步表明,QHTFC治疗HUA的主要途径涉及IL-17信号通路。体内实验结果显示,QHTFC通过双向调节尿酸转运蛋白,在高尿酸血症模型中发挥了有效的降尿酸作用。从机制上讲,QHTFC抑制肝脏XOD活性,从而减少尿酸的产生。此外,它通过上调OAT1和ABCG2转运蛋白促进尿酸排泄,并通过下调GLUT9和URAT1表达抑制重吸收。我们的研究结果表明,QHTFC可以显著降低血清UA水平,并通过调节氧化应激、炎症和肾纤维化来改善肾损伤。本研究为QHTFC在高尿酸血症治疗中的应用提供了新的证据。
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来源期刊
CiteScore
3.10
自引率
5.60%
发文量
327
审稿时长
7.5 months
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: Target identification and validation Assay design, development, miniaturization and comparison High throughput/high content/in silico screening and associated technologies Label-free detection technologies and applications Stem cell technologies Biomarkers ADMET/PK/PD methodologies and screening Probe discovery and development, hit to lead optimization Combinatorial chemistry (e.g. small molecules, peptide, nucleic acid or phage display libraries) Chemical library design and chemical diversity Chemo/bio-informatics, data mining Compound management Pharmacognosy Natural Products Research (Chemistry, Biology and Pharmacology of Natural Products) Natural Product Analytical Studies Bipharmaceutical studies of Natural products Drug repurposing Data management and statistical analysis Laboratory automation, robotics, microfluidics, signal detection technologies Current & Future Institutional Research Profile Technology transfer, legal and licensing issues Patents.
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