Suppr超能文献

盐酸苄丝肼单独及与氟康唑联合抗. 的抗真菌作用及潜在机制。

Antifungal Effects and Potential Mechanisms of Benserazide Hydrochloride Alone and in Combination with Fluconazole Against .

机构信息

Department of Clinical Pharmacy, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Shandong Engineering and Technology Research Center for Pediatric Drug Development, Shandong Medicine and Health Key Laboratory of Clinical Pharmacy, Jinan, People's Republic of China.

Department of Pharmacy, China-Japan Friendship Hospital, Beijing, People's Republic of China.

出版信息

Drug Des Devel Ther. 2021 Nov 16;15:4701-4711. doi: 10.2147/DDDT.S336667. eCollection 2021.

Abstract

PURPOSE

The resistance of to traditional antifungal drugs brings a great challenge to clinical treatment. To overcome the resistance, developing antifungal agent sensitizers has attracted considerable attention. This study aimed to determine the anti- activity of BEH alone or BEH-FLC combination and to explore the underlying mechanisms.

MATERIALS AND METHODS

In vitro antifungal effects were performed by broth microdilution assay and XTT reduction assay. Infected larvae model was used to determine the antifungal effects in vivo. Probes Fluo-3/AM, FITC-VAD-FMK and rhodamine 6G were used to study the influence of BEH and FLC on intracellular calcium concentration, metacaspase activity and drug efflux of .

RESULTS

BEH alone exhibited obvious antifungal activities against . BEH plus FLC not only showed synergistic effects against planktonic cells and preformed biofilms within 8 h but also enhanced the antifungal activity in infected larvae. Mechanistic studies indicated that antifungal effects of drugs might be associated with the increasement of calcium concentration, activation of metacaspase activity to reduce virulence and anti-biofilms, but were not related to drug efflux.

CONCLUSION

BEH alone or combined with FLC displayed potent antifungal activity both in vitro and in vivo, and the underlying mechanisms were related to reduced virulence factors.

摘要

目的

对传统抗真菌药物的耐药性给临床治疗带来了巨大挑战。为了克服耐药性,开发抗真菌药物敏化剂引起了相当大的关注。本研究旨在确定 BEH 单独或 BEH-FLC 联合的抗 活性,并探讨其潜在机制。

材料和方法

通过肉汤微量稀释法和 XTT 还原法进行体外抗真菌作用研究。采用 幼虫感染模型来确定体内的抗真菌作用。使用 Fluo-3/AM、FITC-VAD-FMK 和 rhodamine 6G 探针来研究 BEH 和 FLC 对 细胞内钙离子浓度、半胱天冬酶活性和药物外排的影响。

结果

BEH 单独对 表现出明显的抗真菌活性。BEH 加 FLC 不仅在 8 小时内对浮游细胞和已形成的生物膜表现出协同作用,而且增强了感染 幼虫中的抗真菌活性。机制研究表明,药物的抗真菌作用可能与钙离子浓度的增加、降低毒力和抗生物膜的半胱天冬酶活性的激活有关,但与药物外排无关。

结论

BEH 单独或与 FLC 联合在体外和体内均显示出强大的抗真菌活性,其潜在机制与降低毒力因子有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32ae/8605804/adaa45ad57d9/DDDT-15-4701-g0001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验