首页|期刊导航|菌物学报|基于网络药理学、分子对接和实验验证探究蝉花核苷提取物治疗日光性皮炎的作用机制

基于网络药理学、分子对接和实验验证探究蝉花核苷提取物治疗日光性皮炎的作用机制OA

Exploring the mechanism of Cordyceps chanhua nucleoside extract against solar dermatitis based on network pharmacology,molecular docking and experimental verification

中文摘要英文摘要

为了挖掘蝉花核苷提取物抗日光性皮炎的新应用及机制,我们通过网络药理学以及分子对接来筛选蝉花核苷类成分与日光性皮炎的作用靶点,并且对作用机制进行深入分析.同时通过小鼠动物实验验证网络药理学的分析结果.研究结果表明,胸腺嘧啶、腺嘌呤、N6-(2羟乙基)腺苷、肌苷、腺苷是蝉花治疗日光性皮炎的主要活性核苷类成分.TNF、IL1β、AKT1、IL6、INS、IFNG、EGFR、PTGS2、CTNNB1、MAPK1 是蝉花核苷类成分治疗日光性皮炎的核心靶点.富集分析结果显示,PI3K-Akt、TNF、MAPK、IL-17 信号通路是蝉花核苷类成分治疗日光性皮炎的主要生物机制通路.分子对接分析表明,蝉花的主要活性核苷成分与核心靶点之间存在较强的结合亲和力.动物实验验证了蝉花核苷皮肤给药提高了小鼠皮肤组织中的胶原蛋白含量、SOD 抗氧化酶活力,降低了PTGS2含量和TNF-ɑ、IL-1β、IL-17炎症因子水平.Western blotting结果表明,蝉花核苷提取物抑制了p38 MAPK和MMP9 的释放,其分子机制可能与MAPK信号通路有关.研究结果为开发抗日光性皮炎的天然药物提供了新的依据.

In order to explore the new application and mechanism of action of Cordyceps chanhua nucleoside extracts on solar dermatitis,the targets of C.chanhua nucleoside components treating solar dermatitis were screened by network pharmacology and molecular docking.The results of network pharmacology analysis were verified by mouse animal experiments.The results showed that thymine,adenine,N6-(2 hydroxyethyl)adenosine,inosine and adenosine were the main active nucleoside components of C.chanhua in the treatment of solar dermatitis,and TNF,IL1β,AKT1,IL6,INS,IFNG,EGFR,PTGS2,CTNNB1,and MAPK1 were the core targets of C.chanhua nucleoside components.Enrichment analysis showed that PI3K-Akt,TNF,MAPK and IL-17 signaling pathways were the major biomechanistic pathways of C.chanhua nucleoside components for the treatment of solar dermatitis.Molecular docking analysis showed that there was a strong binding affinity between the main active components of C.chanhua nucleoside components and the core targets.Animal experiments verified that dermal administration of C.chanhua increased collagen content and SOD antioxidant enzyme activity,and decreased PTGS2 content and levels of TNF-ɑ,IL-1β,and IL-17 inflammatory factors in mouse skin tissues.The results of Western blotting showed that C.chanhua nucleoside extracts inhibited the release of p38 MAPK and MMP9,and the molecular mechanism might be related to the MAPK signaling pathway.This study provides a new basis for the development of natural drugs against solar dermatitis.

马悦文;李薇;叶向露;龙文君;王玉芹;王春丽

华东理工大学药学院 制药工程与过程化学教育部工程研究中心 上海市新药设计重点实验室,上海 200237华东理工大学药学院 制药工程与过程化学教育部工程研究中心 上海市新药设计重点实验室,上海 200237泛亚生物医药股份有限公司 浙江泛亚生命科学研究院,浙江 平湖 314200||上海泛亚生命科学研究院,上海 200237泛亚生物医药股份有限公司 浙江泛亚生命科学研究院,浙江 平湖 314200||上海泛亚生命科学研究院,上海 200237泛亚生物医药股份有限公司 浙江泛亚生命科学研究院,浙江 平湖 314200||上海泛亚生命科学研究院,上海 200237华东理工大学药学院 制药工程与过程化学教育部工程研究中心 上海市新药设计重点实验室,上海 200237

网络药理学分子对接小鼠实验蝉花核苷日光性皮炎

network pharmacologymolecular dockingmurine experimentCordyceps chanhua nucleosidessolar dermatitis

《菌物学报》 2026 (3)

88-105,18

国家科技重大专项(2018ZX09735002) This work was supported by the National Key Technology Research and Development Program(2018ZX09735002).

10.13346/j.mycosystema.250215

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