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减轻耐青霉素肺炎链球菌诱导的肺上皮细胞损伤:银花平感颗粒主要成分优化组合作用机制的深入研究

Alleviating penicillin-resistant Streptococcus pneumoniae‑induced lung epithelial cell injury: mechanistic insights into effects of the optimized combination of main components from Yinhuapinggan granules.

作者信息

Lv Jiangbo, Wan Haofang, Yu Daojun, Zhou Huifen, Wang Wenba, Wan Haitong

机构信息

College of Chinese Medicine for Cardiovascular-Cranial Disease, Zhejiang Chinese Medical University, Hangzhou, China.

Zhejiang Key Laboratory of Chinese Medicine for Cardiovascular and Cerebrovascular Disease, Hangzhou, China.

出版信息

BMC Infect Dis. 2025 Apr 20;25(1):565. doi: 10.1186/s12879-025-10951-1.

Abstract

OBJECTIVE

Penicillin-resistant Streptococcus pneumoniae (PRSP), for which novel treatment medicines are required, has expanded extensively due to the overuse of antibiotics. This study aimed to detect the optimal ratio of the combination of the main components based on Yinhuapinggan granules (YHPG) to generate novel treatment concepts for PRSP-induced lung injury.

METHODS

Three representative main components: chlorogenic acid (C), amygdalin (A), and puerarin (P) were selected, and the optimal combination of these three components was determined by an orthogonal experiment. Investigations were conducted on the potential mechanisms underlying the protective effect of this optimized combination against PRSP-induced lung epithelial cell damage. Meanwhile, the bacteriostatic effect was further explored through the optimized combination of these natural products combined with penicillin G (PG).

RESULTS

The optimized combination CAP (C: 16 µg/mL, A: 24 µg/mL, P: 24 µg/mL) screened by the orthogonal experimental design reduced cell damage in a model of human lung epithelial cells infected by PRSP, and the combination of CAP and PG had a synergistic effect. At the cellular level, CAP attenuated lung epithelial cell injury by modulating the TLRs/MyD88 inflammatory pathway. At the bacterial level, CAP modulated the virulence and drug resistance of PRSP, resulting in enhanced bacterial inhibition by the combination of CAP and PG.

CONCLUSION

Taken together, our results suggest that CAP can modulate or synergize with PG to modulate the TLRs/MyD88 pathway and attenuate PRSP-induced lung injury, and can be used as a potential drug for treating PRSP infection.

摘要

目的

由于抗生素的过度使用,对新型治疗药物有需求的耐青霉素肺炎链球菌(PRSP)已广泛传播。本研究旨在检测基于银花平感颗粒(YHPG)的主要成分组合的最佳比例,以产生针对PRSP诱导的肺损伤的新型治疗理念。

方法

选择三种代表性的主要成分:绿原酸(C)、苦杏仁苷(A)和葛根素(P),通过正交试验确定这三种成分的最佳组合。对这种优化组合对PRSP诱导的肺上皮细胞损伤的保护作用的潜在机制进行了研究。同时,通过这些天然产物与青霉素G(PG)的优化组合进一步探索抑菌作用。

结果

通过正交实验设计筛选出的优化组合CAP(C:16μg/mL,A:24μg/mL,P:24μg/mL)减少了PRSP感染的人肺上皮细胞模型中的细胞损伤,并且CAP与PG的组合具有协同作用。在细胞水平上,CAP通过调节TLRs/MyD88炎症途径减轻肺上皮细胞损伤。在细菌水平上,CAP调节PRSP的毒力和耐药性,导致CAP与PG组合增强细菌抑制作用。

结论

综上所述,我们的结果表明,CAP可以调节或与PG协同调节TLRs/MyD88途径并减轻PRSP诱导的肺损伤,并且可以用作治疗PRSP感染的潜在药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8e4/12010621/c417044fe23d/12879_2025_10951_Fig1_HTML.jpg

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