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Therapeutic potential of botanical drugs and their metabolites in the treatment of pelvic inflammatory disease

Affiliation
School of Clinical Medicine ,Chengdu University of Traditional Chinese Medicine ,Chengdu ,China
Zhong, Han-Zhi;
Affiliation
School of Clinical Medicine ,Chengdu University of Traditional Chinese Medicine ,Chengdu ,China
Yan, Pei-Jia;
Affiliation
School of Clinical Medicine ,Chengdu University of Traditional Chinese Medicine ,Chengdu ,China
Gao, Qi-Feng;
Affiliation
School of Clinical Medicine ,Chengdu University of Traditional Chinese Medicine ,Chengdu ,China
Wu, Jue;
Affiliation
Department of Gynecology ,Hospital of Chengdu University of Traditional Chinese Medicine ,Chengdu ,China
Ji, Xiao-Li;
Affiliation
Department of Gynecology ,Hospital of Chengdu University of Traditional Chinese Medicine ,Chengdu ,China
Wei, Shao-Bin

The application of botanical drugs and their metabolites in the treatment of pelvic inflammatory disease (PID) has garnered significant attention. Owing to their broad-spectrum activity, global accessibility, and structural diversity, botanical drugs have emerged as promising candidates for adjunctive or alternative therapies. This review systematically summarizes botanical drugs and their metabolites, focusing on their antimicrobial potential against endogenous and exogenous pathogens associated with PID. Specifically, it addresses various underlying antibacterial mechanisms, including interference with bacterial cell membranes and cell walls, inhibition of pathogen-specific efflux pumps, modulation of pathogen-related gene expression, and synergistic effects when combined with conventional antibiotics. This review highlights the therapeutic promise of botanical drugs and their metabolites, emphasizing critical findings regarding their inhibitory effects on PID-associated pathogens. Such insights provide valuable guidance for future therapeutic strategies and may support ongoing antibiotic discovery and development.

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License Holder: Copyright © 2025 Zhong, Yan, Gao, Wu, Ji and Wei.

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