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Synergistic Effect of Fluconazole and Calcium Channel Blockers against Resistant Candida albicans

机译:氟康唑和钙通道阻滞剂对抗白色念珠菌的协同作用

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摘要

Candidiasis has increased significantly recently that threatens patients with low immunity. However, the number of antifungal drugs on the market is limited in comparison to the number of available antibacterial drugs. This fact, coupled with the increased frequency of fungal resistance, makes it necessary to develop new therapeutic strategies. Combination drug therapy is one of the most widely used and effective strategy to alleviate this problem. In this paper, we were aimed to evaluate the combined antifungal effects of four CCBs (calcium channel blockers), amlodipine (AML), nifedipine (NIF), benidipine (BEN) and flunarizine (FNZ) with fluconazole against C. albicans by checkerboard and time-killing method. In addition, we determined gene (CCH1, MID1, CNA1, CNB1, YVC1, CDR1, CDR2 and MDR1) expression by quantitative PCR and investigated the efflux pump activity of resistant candida albicans by rhodamine 6G assay to reveal the potential mechanisms. Finally, we concluded that there was a synergy when fluconazole combined with the four tested CCBs against resistant strains, with fractional inhibitory concentration index (FICI) <0.5, but no interaction against sensitive strains (FICI = 0.56 ~ 2). The mechanism studies revealed that fluconazole plus amlodipine caused down-regulating of CNA1, CNB1 (encoding calcineurin) and YVC1 (encoding calcium channel protein in vacuole membrane).
机译:最近,念珠菌病显着增加,威胁到免疫力低下的患者。然而,与可用的抗菌药物的数量相比,市场上抗真菌药物的数量是有限的。这一事实,加上真菌耐药性频率的增加,使得有必要开发新的治疗策略。联合药物疗法是缓解该问题最广泛使用和有效的策略之一。在本文中,我们旨在评估四种CCB(钙通道阻滞剂),氨氯地平(AML),硝苯地平(NIF),贝尼地平(BEN)和氟硝利嗪(FNZ)与氟康唑对白念珠菌的联合抗真菌作用。消磨时间的方法。此外,我们通过定量PCR确定了基因(CCH1,MID1,CNA1,CNB1,YVC1,CDR1,CDR2和MDR1)的表达,并通过若丹明6G分析法研究了抗性白色念珠菌的外排泵活性,以揭示其潜在机制。最后,我们得出的结论是,氟康唑与四种经过测试的CCB联合使用具有抗药性,分数抑制浓度指数(FICI)<0.5,但与敏感菌株无相互作用(FICI = 0.56〜2)。机理研究表明,氟康唑加氨氯地平导致CNA1,CNB1(编码钙调神经磷酸酶)和YVC1(液泡膜中编码钙通道蛋白)的下调。

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