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Novel synergism of two antifungal agents copiamycin and imidazole.

机译:两种抗真菌药考皮霉素和咪唑的新型协同作用。

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摘要

Copiamycin, a macrocyclic lactone antifungal antibiotic, was found to potentiate the antifungal effect of imidazole compounds, ketoconazole in particular. The potentiation of two nominally fungistatic agents in vitro was substantiated by a marked reduction of the minimum inhibitory and minimum fungicidal concentrations when the drugs were used in combination. The effectiveness of this synergistic combination was also demonstrated in experimental murine candidosis. Evidence is presented to suggest that this combined effect is due, at least in part, to the ionophoretic property of copiamycin. Whereas amphotericin B induces a marked increase in cellular permeability, this antibiotic does not possess the ionophoretic action of copiamycin, indicating that the enhancement of copiamycin activity and significant reduction of amphotericin B activity by ketoconazole pretreatment can be ascribed not only to changes in membrane permeability of the test organisms, but also to the different action mechanisms of copiamycin and amphotericin B. It is thus plausible that the strong synergism of copiamycin with imidazole compounds is related to the ionophoretic activity of the antibiotic. Further studies on the biochemical mechanism of this synergistic effect are being conducted together with an assessment of the clinical significance of this drug combination.
机译:已发现大环内酯类抗真菌抗生素Copiamycin增强了咪唑化合物(尤其是酮康唑)的抗真菌作用。当两种药物组合使用时,最小抑制和最小杀菌浓度的显着降低证实了两种名义上的抑菌剂在体外的增强作用。实验鼠念珠菌病也证明了这种协同组合的有效性。已有证据表明这种联合作用至少部分是由于卡波霉素的离子电特性引起的。尽管两性霉素B诱导细胞通透性显着增加,但该抗生素不具有copiamycin的离子运动作用,这表明酮康唑预处理使copiamycin活性增强和两性霉素B活性显着降低,不仅可以归因于其膜通透性的变化。因此,可以认为卡波霉素与咪唑化合物的强协同作用与抗生素的离子电活性有关。对该协同作用的生化机理进行了进一步研究,并对该药物组合的临床意义进行了评估。

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