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Active components and molecular mechanism of Syringa oblata Lindl. in the treatment of endometritis based on pharmacology network prediction

子宫内膜炎 木犀草素 化学 芦丁 金黄色葡萄球菌 药理学 山奈酚 柚皮素 传统医学 生物化学 生物 医学 细菌 槲皮素 类黄酮 抗氧化剂 怀孕 遗传学
作者
Xiao-Zhen Wang,Xue-Jiao Song,Chang Liu,Chen Xing,Tong Wu,Yue Zhang,Jing Su,Jing-You Hao,Xue-Ying Chen,Zhi-Yun Zhang,Yan-Hua Li,Yan-Yan Liu
出处
期刊:Frontiers in Veterinary Science [Frontiers Media]
卷期号:9
标识
DOI:10.3389/fvets.2022.885952
摘要

Antibiotic treatment of endometritis was limited by the inevitable antibiotic residues and risk of bacterial resistance. Therefore, the development of safe and effective strategies for endometritis treatment is urgently needed. Syringa oblata Lindl. (SOL) showed great pharmacological potential against endometritis. However, the active components and underlying mechanism of SOL for endometritis treatment remain indeterminate. In our study, the active components and possible molecular mechanism of SOL against endometritis were predicted through computer data mining and biological networks construction. It was predicted that the main active components of SOL were luteolin, kaempferol, oleanolic acid, and rutin, and their anti-endometritis effect was mainly attributed to the TLRs/NF-κB signaling pathway. Furthermore, a green and efficient deep eutectic solvent combined with ultrasound-assisted extraction (DES-UAE) was performed and optimized to obtain high contents of total flavonoid, rutin, and luteolin. The four predicted active components in the SOL extracts were qualitatively and quantitatively analyzed by LC/MS and HPLC. Finally, the pharmacological effects of SOL and active components have been verified by Staphylococcus aureus -endometritis models in mice. H&E staining and bacterial load in uterus tissues assays initially validated the pharmacodynamic effects of SOL, and quantitative real-time PCR (RT-qPCR) and ELISA results confirmed that SOL and four active components could ameliorate the uterus injury caused by Staphylococcus aureus , the mechanism of action is related to the TLRs/NF-κB signaling pathway.

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