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利用网络药理学等工具研究厚朴大黄汤治疗化脓性链球菌皮肤感染的活性成分及作用机制。

Utilizing network pharmacology and other tools to examine active components and mechanism of action of Magnolia officinalis rheum rhabarbarum decoction in treating Streptococcus pyogenes skin infections.

作者信息

Wang Yuanhao, Wang Xinrui, Zhang Xueying, Pan Mengyi, Sun Mingyang, Chen Zhiguo, Song Yingli

机构信息

School of Basic Medical Sciences, Harbin Medical University, No. 157, Health Care Road, Nangang District, Harbin City, Heilongjiang Province, China.

The Second Affiliated Hospital of Harbin Medical University, No.246 Xuefu Road, Nangang District, Harbin City, Heilongjiang Province, China.

出版信息

Bioresour Bioprocess. 2025 Aug 26;12(1):92. doi: 10.1186/s40643-025-00933-1.

Abstract

Infections caused by Streptococcus pyogenes and the growing threat of antibiotic resistance pose significant global health challenges. This study investigates the antibacterial properties of Magnolia officinalis Rheum rhabarbarum Decoction against Streptococcus pyogenes skin infections. By combining UHPLC-MS/MS, network pharmacology, and molecular docking techniques, we identified eight bioactive compounds in the formulation and explored their potential interactions with Streptococcus pyogenes-related targets. Our analysis revealed that compounds such as Sinensetin, Nobiletin, and (+)-Magnoflorine regulate immune pathways (IL-17, TNF), inhibit the production of inflammatory factors, and disrupt bacterial membranes and metabolic processes, achieving dual antibacterial and anti-inflammatory effects. In vitro experiments showed that the decoction exhibited a minimum inhibitory concentration (MIC) of 20 mg/mL against Streptococcus pyogenes, significantly reducing the secretion of pro-inflammatory factors such as IL-1α, IL-6, IL-36, and TNF-α. These results suggest that Magnolia officinalis Rheum rhabarbarum Decoction offers a promising multi-target strategy for treating drug-resistant Streptococcus pyogenes infections and may serve as a potential alternative to traditional antibiotics.

摘要

化脓性链球菌引起的感染以及抗生素耐药性日益增长的威胁给全球健康带来了重大挑战。本研究调查了厚朴大黄汤对化脓性链球菌皮肤感染的抗菌特性。通过结合超高效液相色谱-串联质谱、网络药理学和分子对接技术,我们鉴定出该方剂中的8种生物活性化合物,并探索了它们与化脓性链球菌相关靶点的潜在相互作用。我们的分析表明,诸如橙皮素、川陈皮素和(+)-木兰碱等化合物可调节免疫途径(IL-17、TNF),抑制炎症因子的产生,并破坏细菌膜和代谢过程,从而实现抗菌和抗炎双重作用。体外实验表明,该汤剂对化脓性链球菌的最低抑菌浓度(MIC)为20mg/mL,显著降低了IL-1α、IL-6、IL-36和TNF-α等促炎因子的分泌。这些结果表明,厚朴大黄汤为治疗耐药性化脓性链球菌感染提供了一种有前景的多靶点策略,可能成为传统抗生素的潜在替代品。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7498/12381315/74cbc75af927/40643_2025_933_Fig1_HTML.jpg

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