白芍通过调节 M2 巨噬细胞极化,有效减轻何首乌诱导的特发性肝损伤

Ye Xiu, Zhixin Wu, Yichong Chen, Wenqing Mu, Xiaomei Zhao, Ming Dong, Yurong Li, Zhaofang Bai, Xiaohe Xiao
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引用次数: 0

摘要

何首乌(Polygonum multiflorum Thunb.,PM)是一种常用的滋补药材,已知会导致特异性药物性肝损伤(IDILI)。本研究探讨了白芍(PRA)对PM诱导的特发性药物性肝损伤(IDILI)的解毒作用和潜在作用机制。 研究利用网络药理学分析预测了 "PRA-PM-innate 免疫 "的相关靶点。采用非肝毒性脂多糖(LPS)和PM诱导的IDILI模型,通过测定肝功能指标、病理检查和巨噬细胞相关因子来评估PRA的解毒作用。用IL-4刺激骨髓源性巨噬细胞(BMDMs)分化为M2巨噬细胞,探讨PM和PRA对M2巨噬细胞极化的影响。 PRA-PM-鞘氨醇免疫 "的靶点筛选发现了21个交叉靶点,其中大部分与巨噬细胞极化密切相关。在PM诱导的大鼠IDILI模型中,联合使用PRA能显著降低肝损伤程度和炎症因子水平,同时促进IL-4、IL-10、Arg1和CD206等M2巨噬细胞相关因子的表达。在体外,PM 可剂量依赖性地抑制 Arg1 蛋白和 M2 巨噬细胞相关基因的表达,而 PRA 则表现出相反的效果。当联合使用时,PRA 可改善 PM 对 M2 巨噬细胞极化的抑制作用。 我们的研究结果表明,PRA 对 PM 诱导的 IDILI 有治疗作用;其机制可能是通过促进 M2 巨噬细胞极化来减轻肝损伤,从而减少炎症因子的表达。
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Paeoniae Radix Alba effectively attenuates Polygonum multiflorum Thunb. -induced idiosyncratic liver injury by modulating M2 macrophage polarization
Polygonum multiflorum Thunb. (PM) is a commonly used tonic herb known to cause idiosyncratic drug-induced liver injury (IDILI). This study explored the detoxification effects and potential mechanisms of action of Paeoniae Radix Alba (PRA) on PM-induced IDILI. Network pharmacology analysis was utilized to predict the related targets of "PRA-PM-innate immunity.” A non-hepatotoxic lipopolysaccharide (LPS) and PM-induced IDILI model was used to evaluate the detoxification effects of PRA by measuring liver function indicators, pathological examinations, and macrophage-related factors. Bone marrow-derived macrophages (BMDMs) were stimulated with IL-4 to differentiate into M2 macrophages, and the effects of PM and PRA on M2 macrophage polarization were explored. Target screening of "PRA-PM-innate immunity" identified 21 intersecting targets, most of which were closely associated with macrophage polarization. In rat models of IDILI induced by PM, the combined use of PRA significantly reduced the extent of liver damage and the levels of inflammatory factors, while promoting the expression of M2 macrophage-related factors such as IL-4, IL-10, Arg1, and CD206. In vitro, PM dose-dependently inhibited the expression of the Arg1 protein and M2 macrophage-related genes, whereas PRA exhibited the opposite effect. When used in combination, PRA ameliorated the inhibitory effect of PM on M2 macrophage polarization. Our results demonstrate that PRA has a therapeutic effect on PM-induced IDILI; its mechanism may involve alleviating liver injury by promoting M2 macrophage polarization, thus reducing the expression of inflammatory factors.
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