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绞股蓝总苷与氟康唑联合抗耐药白念珠菌的协同作用:通过抑制药物外排和生物膜形成。

The synergistic antifungal effects of gypenosides combined with fluconazole against resistant Candida albicans via inhibiting the drug efflux and biofilm formation.

机构信息

Department of Clinical Pharmacy, the First Affiliated Hospital of Shandong First Medical University, Jinan, People's Republic of China.

School of Pharmaceutical Sciences, Shandong First Medical University & Shandong Academy of Medical Sciences, Taian, Shandong Province, People's Republic of China.

出版信息

Biomed Pharmacother. 2020 Oct;130:110580. doi: 10.1016/j.biopha.2020.110580. Epub 2020 Jul 31.

DOI:10.1016/j.biopha.2020.110580
PMID:32745913
Abstract

The increased resistance of Candida to conventional antifungals brings great challenges for the clinical treatment of Candida infections. Recently, more attention has been paid to the research on combination therapy, which is a potential therapeutic approach for overcoming Candida resistance. In the present study, we first investigated the interaction between gypenosides (Gyp) and fluconazole (FLC) against Candida albicans (C. albicans) in vitro and in vivo. The in vitro test revealed a synergistic antifungal activity between Gyp and FLC against FLC-resistant (FLC) C. albicans and indifferent effects for FLC-susceptible (FLC) C. albicans, with the fractional inhibitory concentration index of 0.2539-0.2578 and 1-1.5, respectively. Besides, Gyp displayed synergistic interaction with FLC against FLCC. albicans performed biofilm over 4 h, with the fractional inhibitory concentration index <0.5. In vivo, the combined antifungal efficacy of Gyp with FLC was evaluated by Galleria mellonella (G. mellonella) larvae. Gyp plus FLC prolonged the survival rate and reduced tissue invasion of larvae infected with FLCC. albicans. Further experiments to get a first hint at what antifungal mechanisms might be inhibition of early biofilm formation, suppression of drug efflux, and inhibition of yeast-hyphal conversion. These findings will provide a new approach for the treatment of C. albicans infection.

摘要

念珠菌对常规抗真菌药物的耐药性增加给念珠菌感染的临床治疗带来了巨大挑战。最近,人们越来越关注联合治疗的研究,这是克服念珠菌耐药性的一种潜在治疗方法。在本研究中,我们首先研究了绞股蓝总苷(Gyp)与氟康唑(FLC)在体外和体内对白色念珠菌(C. albicans)的相互作用。体外试验显示,Gyp 与 FLC 联合使用对氟康唑耐药(FLC)的白色念珠菌具有协同抗真菌活性,而对氟康唑敏感(FLC)的白色念珠菌无影响,其部分抑菌浓度指数分别为 0.2539-0.2578 和 1-1.5。此外,Gyp 与 FLC 联合使用对生物膜形成超过 4 小时的 FLCC. albicans 具有协同作用,部分抑菌浓度指数<0.5。体内,通过大蜡螟(G. mellonella)幼虫评估 Gyp 与 FLC 的联合抗真菌疗效。Gyp 加 FLC 延长了感染 FLCC 的幼虫的存活率并减少了组织侵袭。albicans。进一步的实验初步提示,抗真菌机制可能是抑制早期生物膜形成、抑制药物外排和抑制酵母-菌丝转化。这些发现将为治疗白色念珠菌感染提供新的方法。

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