揭示淫羊藿苷与唑类药物对白色念珠菌的协同作用。

IF 3 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
Frontiers in oral health Pub Date : 2025-02-13 eCollection Date: 2025-01-01 DOI:10.3389/froh.2025.1517210
Barbod Aliaghazadeh, Marina Pascual-Ortiz, Alba Martínez, Veronica Veses, Chirag C Sheth
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引用次数: 0

摘要

简介与方法:本研究探讨淫羊藿属植物中的类黄酮淫羊藿苷与选定的抗真菌药物联合体外对白色念珠菌的协同作用。结果:该黄酮类化合物通过降低氟康唑对白色念珠菌的最低抑制浓度,显著增强氟康唑的体外抑制作用。淫羊藿苷分别与唑族的酮康唑和伊曲康唑联用时也观察到这种作用。有趣的是,当淫羊藿苷与其他种类的抗真菌药物(如两性霉素B或caspofungin)联合使用时,没有观察到增强活性的作用。讨论:基于fun1显微镜和细胞壁和细胞膜应激源共孵育的结果,我们得出结论,淫羊藿苷可能通过细胞膜介导的机制增加白色念珠菌对唑的敏感性。临床分离株,特别是耐氟康唑的白色念珠菌,需要进一步的研究来探索这些作用,以期淫羊藿苷作为抗真菌唑治疗的辅助剂在临床中的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unveiling the synergistic effect of icariin and azole drugs on Candida albicans.

Introduction and method: The current study explores the synergistic effects of icariin, a flavonoid found in plants of the genus Epimedium, in ombination with selected antifungal agents, against Candida albicans in vitro.

Results: This flavonoid significantly enhanced the in vitro effect of fluconazole, by decreasing the minimum inhibitory concentration against C. albicans. This effect was also observed when combining icariin with ketoconazole and itraconazole of the azole family respectively. Interestingly, no activity-enhancing effect was observed when icariin was combined with other classes of antifungals, such as amphotericin B or caspofungin.

Discussion: We conclude that icariin may increase the sensitivity of C. albicans to azoles via a cell membrane mediated mechanism, based on our results from FUN-1 microscopy and coincubation with cell wall and cell membrane stressors. Further research is required to explore these effects in clinical isolates, particularly fluconazole-resistant C. albicans, with a view towards the clinical application of icariin as a co-adjuvant in antifungal azole therapy.

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来源期刊
CiteScore
3.30
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