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苦参中的芒柄花黄素通过抑制中性粒细胞胞外诱捕网减轻特应性皮炎。

Formononetin From Sophora flavescens Aiton Alleviates Atopic Dermatitis by Suppressing Neutrophil Extracellular Traps.

作者信息

Cheng Lin, Du Zhirui, Yan Xueqiao, Che Manju, Zhi Guoguo, Ma Xiuying, Geng Funeng, Li Baojie

机构信息

Institute of Traditional Chinese Medicine and Stem Cell Research, College of Basic Medical Sciences, Chengdu University of Traditional Chinese Medicine, Chengdu, China.

Demonstrations Center for Experimental Teaching in Biomedicine, School of Bioscience and Technology, Chengdu Medical College, Chengdu, China.

出版信息

Phytother Res. 2025 Aug;39(8):3784-3799. doi: 10.1002/ptr.70020. Epub 2025 Jul 10.

Abstract

Atopic dermatitis (AD) is a chronic inflammatory skin disorder with limited effective treatment. Sophora flavescens Aiton (Kushen) exhibits anti-inflammatory properties, but its key active components and mechanisms against AD remain unclear. This study aimed to identify its therapeutic compounds and the underlying molecular mechanisms. Network pharmacology and ultra-performance liquid chromatography quadrupole time-of-flight mass spectrometry were applied to screen for the potential bioactive compounds from Kushen, which were validated in AD mouse models. Formononetin (FMN) was topically administered to evaluate its curative efficacy through histopathological and immunofluorescent staining of skin lesions. Transcriptomic profiling explored the molecular mechanisms, with subsequent validation of neutrophil extracellular traps (NETs)-associated markers by immunofluorescent staining and western blotting. Co-treatment with PAD4 inhibitor GSK484 and molecular docking were used to study the underlying mechanisms. The study identified FMN as an important active component in Kushen, which showed therapeutic effects comparable to dexamethasone in AD models. FMN normalized cutaneous hyperplasia, reduced infiltration of CD3 T cells, mast cells, and neutrophils, and suppressed inflammatory cytokine expression. Mechanistically, FMN inhibited NETs formation evidenced by decreased levels of citrullinated histone H3 (citH3), myeloperoxidase (MPO), and peptidylarginine deiminase 4 (PAD4). GSK484 co-treatment showed non-synergistic effects, suggesting that FMN suppresses NETs formation primarily through PAD4/MPO inhibition, which was confirmed by molecular docking. These findings highlight FMN as a primary anti-AD constituent of Kushen, therapeutically suppressing NETs-driven crosstalk of innate and adaptive immunity. FMN's multitarget mechanisms provide mechanistic insights and position it as a candidate for AD treatment.

摘要

特应性皮炎(AD)是一种慢性炎症性皮肤病,有效治疗方法有限。苦参具有抗炎特性,但其抗AD的关键活性成分和机制尚不清楚。本研究旨在确定其治疗性化合物及其潜在的分子机制。应用网络药理学和超高效液相色谱四极杆飞行时间质谱法从苦参中筛选潜在的生物活性化合物,并在AD小鼠模型中进行验证。局部应用芒柄花素(FMN),通过对皮肤病变进行组织病理学和免疫荧光染色来评估其疗效。转录组分析探索分子机制,随后通过免疫荧光染色和蛋白质印迹法验证中性粒细胞胞外陷阱(NETs)相关标志物。联合使用PAD4抑制剂GSK484和分子对接来研究潜在机制。该研究确定FMN是苦参中的一种重要活性成分,在AD模型中显示出与地塞米松相当的治疗效果。FMN使皮肤增生正常化,减少CD3 T细胞、肥大细胞和中性粒细胞的浸润,并抑制炎性细胞因子表达。机制上,FMN抑制NETs形成,表现为瓜氨酸化组蛋白H3(citH3)、髓过氧化物酶(MPO)和肽基精氨酸脱亚氨酶4(PAD4)水平降低。GSK484联合治疗显示无协同作用,表明FMN主要通过抑制PAD4/MPO来抑制NETs形成,分子对接证实了这一点。这些发现突出了FMN作为苦参抗AD的主要成分,在治疗上抑制NETs驱动的固有免疫和适应性免疫的相互作用。FMN的多靶点机制提供了机制性见解,并使其成为AD治疗的候选药物。

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