Therapeutic effects and mechanisms of Juanbilijieqing fang in ameliorating gouty arthritis in a murine model.

IF 2.2 4区 医学 Q3 TOXICOLOGY Toxicology Research Pub Date : 2025-01-17 eCollection Date: 2025-02-01 DOI:10.1093/toxres/tfaf005
Biao Zhou, Wei Li, Zhiqiang Luo, Liguo Zhu, Jie Yu, Yuxing Guo, Wangyang Li, Hui Xiong, Xiaolong Lu
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Abstract

This study aims to assess the safety, efficacy, and mechanisms of Juanbilijieqing Fang in a mouse model of gouty arthritis. C57BL/6 mice were allocated into six groups: control, gouty arthritis model, and treatment groups receiving varying doses of Juanbilijieqing Fang (low, medium, high), along with a positive control group treated with febuxostat. Gouty arthritis was induced via MSU crystal injection following a high-fat diet. Mice were treated with Juanbilijieqing Fang or febuxostat, and safety was evaluated by measuring spleen, kidney, and liver indices. Efficacy was assessed by monitoring foot thickness, pain threshold, and biochemical markers, including serum uric acid (UA), myeloperoxidase (MPO), xanthine oxidase (XOD), and adenosine deaminase (ADA). Serum pro-inflammatory cytokines were analyzed, and intestinal inflammation and barrier integrity were examined through histological and molecular assays. Juanbilijieqing Fang did not significantly affect spleen, kidney, or liver indices, indicating its safety. Therapeutically, it significantly reduced foot swelling, improved pain threshold, and decreased serum uric acid levels. It also lowered MPO activity in foot tissue and reduced XOD and ADA activity in the liver. Additionally, the formula downregulated pro-inflammatory cytokines, such as IL-1α, IL-1β, IL-6, TNF-α, and IFN-γ, demonstrating a strong anti-inflammatory effect. It ameliorated gut inflammation by decreasing NLRP3 inflammasome components (NLRP3, ASC, and Caspase-1) and enhanced gut mucosal integrity by upregulating ZO-1 and Occludin expression. Juanbilijieqing Fang is a safe and effective treatment for gouty arthritis, primarily through reducing systemic and intestinal inflammation and restoring gut barrier function.

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蠲痹痹清方改善小鼠痛风性关节炎的疗效及机制研究。
本研究旨在评价蠲痹解清方对痛风性关节炎小鼠模型的安全性、有效性及其作用机制。将C57BL/6小鼠分为6组:对照组、痛风性关节炎模型组和不同剂量蠲痹解清方(低、中、高)治疗组,阳性对照组给予非布司他治疗。在高脂肪饮食后通过MSU晶体注射诱导痛风性关节炎。小鼠分别给予蠲痹痹清方或非布司他治疗,通过脾、肾、肝指标评价其安全性。通过监测足部厚度、疼痛阈值和生化指标(包括血清尿酸(UA)、髓过氧化物酶(MPO)、黄嘌呤氧化酶(XOD)和腺苷脱氨酶(ADA))来评估疗效。分析血清促炎细胞因子,并通过组织学和分子检测肠道炎症和屏障完整性。蠲痹解清方对脾、肾、肝指标均无显著影响,提示其安全性。治疗上,它显著减少足部肿胀,改善痛阈,降低血清尿酸水平。它还降低足部组织的MPO活性,降低肝脏中的XOD和ADA活性。此外,该配方下调促炎细胞因子,如IL-1α、IL-1β、IL-6、TNF-α和IFN-γ,显示出强大的抗炎作用。它通过降低NLRP3炎性小体成分(NLRP3、ASC和Caspase-1)来改善肠道炎症,并通过上调ZO-1和Occludin表达来增强肠道粘膜完整性。蠲痹痹清方是一种安全有效的治疗痛风性关节炎的药物,主要通过减少全身和肠道炎症,恢复肠道屏障功能。
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来源期刊
Toxicology Research
Toxicology Research TOXICOLOGY-
CiteScore
3.60
自引率
0.00%
发文量
82
期刊介绍: A multi-disciplinary journal covering the best research in both fundamental and applied aspects of toxicology
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