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Ambroxol Hydrochloride Combined with Fluconazole Reverses the Resistance of Candida albicans to Fluconazole

机译:盐酸氨溴索联合氟康唑逆转白色念珠菌对氟康唑的耐药性

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摘要

In this study, we found that ambroxol hydrochloride (128 μg/mL) exhibits synergistic antifungal effects in combination with fluconazole (2 μg/mL) against resistant planktonic Candida albicans (C. albicans) cells. This combination also exhibited synergistic effects against resistant C. albicans biofilms in different stages (4, 8, and 12 h) according to the microdilution method. In vitro data were further confirmed by the success of this combination in treating Galleria mellonella infected by resistant C. albicans. With respect to the synergistic mechanism, our result revealed that ambroxol hydrochloride has an effect on the drug transporters of resistant C. albicans, increasing the uptake and decreasing the efflux of rhodamine 6G, a fluorescent alternate of fluconazole. This is the first study to investigate the in vitro and in vivo antifungal effects, as well as the possible synergistic mechanism of ambroxol hydrochloride in combination with fluconazole against resistant C. albicans. The results show the potential role for this drug combination as a therapeutic alternative to treat resistant C. albicans and provide insights into the development of antifungal targets and new antifungal agents.
机译:在这项研究中,我们发现盐酸氨溴索(128μg/ mL)与氟康唑(2μg/ mL)结合对耐药浮游性白色念珠菌(C. albicans)细胞具有协同抗真菌作用。根据微稀释方法,该组合还显示出在不同阶段(4、8和12 h)对抗白色念珠菌生物膜的协同作用。该组合在治疗抗性白色念珠菌感染的马勒菌中的成功应用进一步证实了体外数据。关于协同机制,我们的结果显示盐酸氨溴索对耐药性白色念珠菌的药物转运蛋白有影响,增加了氟康唑的荧光替代物罗丹明6G的吸收并降低了其流出。这是第一个研究体外和体内抗真菌作用以及氨溴索盐酸盐与氟康唑联合抗白念珠菌的可能协同机制的研究。结果表明该药物组合作为治疗耐药性白色念珠菌的治疗替代品的潜在作用,并为开发抗真菌靶标和新型抗真菌剂提供了见识。

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