Chinese herbal medicines and its active ingredient wogonin can improve immune inflammation in psoriatic arthritis

IF 4.8 2区 医学 Q2 IMMUNOLOGY International immunopharmacology Pub Date : 2025-02-06 DOI:10.1016/j.intimp.2024.113984
Xian-Heng Zhang , Jian Liu , Xiang Ding , Xiao-Lu Chen
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Abstract

Objective

In China, Chinese herbal medicines (CHMs) have been widely used in the treatment of psoriatic arthritis (PsA), showing great therapeutic effects in clinical practice. However, due to the great heterogeneity of PsA and the diversity of CHM combination patterns, there is little high-level evidence-based medical research on the treatment of PsA with CHMs. This study aims to explore the beneficial effects of CHMs on the immune inflammation in PsA and its specific mechanism.

Methods

The data mining method was performed to analyze the real-world data of 91 PsA clinical cases. Network pharmacology, molecular docking, and cellular experiments were used to explore the mechanism of CHMs and its active ingredient wogonin in improving PsA immune inflammation.

Results

Data mining results showed that in PsA, immune inflammation was disturbed and relevant indexes were significantly correlated. After CHM treatment, the level of HCRP, C4, IL-12, IL-17, IL-23, TNF-α, TGF-β1, P65, P50, and IKBα was markedly improved, which was highly correlated with the application of CHMs. In addition, the core prescription containing 10 CHMs was screened, and the action mechanisms of the active ingredient wogonin on the immune inflammation in PsA were identified with network pharmacology and molecular docking. Cell experiments revealed that wogonin reduced M5-induced HaCaT cell viability and TNF-α and IL-1β expressions by blocking the PI3K/AKT pathway in a dose-dependent manner.

Conclusion

Our findings strongly confirmed the enormous promise of CHMs as a therapy for PsA and may provide support for developing drugs and targets for PsA treatment.
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中药及其有效成分枸杞素可改善银屑病关节炎的免疫炎症。
目的:在中国,中草药治疗银屑病关节炎(PsA)已被广泛应用,在临床实践中显示出良好的治疗效果。然而,由于PsA的异质性和中西医结合方式的多样性,目前对中西医结合治疗PsA的高水平循证医学研究很少。本研究旨在探讨中药对PsA免疫炎症的有益作用及其具体机制。方法:采用数据挖掘方法对91例PsA临床病例的真实数据进行分析。采用网络药理学、分子对接、细胞实验等方法,探讨中药及其活性成分枸杞素改善PsA免疫炎症的作用机制。结果:数据挖掘结果显示,在PsA中,免疫炎症受到干扰,相关指标显著相关。中草药治疗后,HCRP、C4、IL-12、IL-17、IL-23、TNF-α、TGF-β1、P65、P50、IKBα水平明显升高,与中草药的应用高度相关。此外,筛选含10种中草药的核心方剂,通过网络药理学和分子对接等方法,确定有效成分乌根素对PsA免疫炎症的作用机制。细胞实验显示,wogonin通过阻断PI3K/AKT通路,以剂量依赖的方式降低m5诱导的HaCaT细胞活力和TNF-α和IL-1β的表达。结论:我们的研究结果有力地证实了中药作为PsA治疗的巨大前景,并可能为PsA治疗的药物和靶点的开发提供支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.40
自引率
3.60%
发文量
935
审稿时长
53 days
期刊介绍: International Immunopharmacology is the primary vehicle for the publication of original research papers pertinent to the overlapping areas of immunology, pharmacology, cytokine biology, immunotherapy, immunopathology and immunotoxicology. Review articles that encompass these subjects are also welcome. The subject material appropriate for submission includes: • Clinical studies employing immunotherapy of any type including the use of: bacterial and chemical agents; thymic hormones, interferon, lymphokines, etc., in transplantation and diseases such as cancer, immunodeficiency, chronic infection and allergic, inflammatory or autoimmune disorders. • Studies on the mechanisms of action of these agents for specific parameters of immune competence as well as the overall clinical state. • Pre-clinical animal studies and in vitro studies on mechanisms of action with immunopotentiators, immunomodulators, immunoadjuvants and other pharmacological agents active on cells participating in immune or allergic responses. • Pharmacological compounds, microbial products and toxicological agents that affect the lymphoid system, and their mechanisms of action. • Agents that activate genes or modify transcription and translation within the immune response. • Substances activated, generated, or released through immunologic or related pathways that are pharmacologically active. • Production, function and regulation of cytokines and their receptors. • Classical pharmacological studies on the effects of chemokines and bioactive factors released during immunological reactions.
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