氟康唑
格尔德霉素
活性氧
氧化应激
两性霉素B
药理学
微生物学
热带假丝酵母
化学
细胞毒性
生物
热休克蛋白90
白色念珠菌
抗真菌
生物化学
体外
热休克蛋白
基因
作者
Chang Jia,Jian Zhang,Yingzhi Zhuge,Ke Xu,Jiahui Liu,Jinle Wang,Lei Li,Maoping Chu
标识
DOI:10.1080/10715762.2019.1610563
摘要
With a significant increase in the incidence of system invasive fungal infections, the limited antifungal drugs and increased frequency of cross-resistance make it necessary to explore new and effective therapeutic strategies. Combination drug therapy has become one widely used choice to alleviate this problem. Geldanamycin (GdA), as an inhibitor of Hsp90, displayed broad antifungal activity when combined with fluconazole. However, due to its cytotoxicity, the dose and duration of GdA is limited. In this study, we observed the effect of fluconazole plus GdA on Candida tropicalis resistant to azoles and amphotericin B. The results showed that this synergism led to a decrease in growth and survival rate. In addition, fluconazole combined with GdA caused mitochondrial depolarisation, disruption of plasma membrane integrity and multinucleated morphology. However, the supplement of a reactive oxygen species (ROS) scavenger, N-acetylcysteine (NAC), rescued the above phenotypes. This study indicated that the oxidative stress mediated by fluconazole plus GdA played an important role in the antifungal activity, and targeting oxidative stress might extend target choices to treat fungal infections.
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