首页> 外文期刊>The Journal of Antibiotics: An International Journal >Enhancement effect of N-methyl-N''-dodecylguanidine on the vacuole-targeting fungicidal activity of amphotericin B against the pathogenic fungus Candida albicans.
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Enhancement effect of N-methyl-N''-dodecylguanidine on the vacuole-targeting fungicidal activity of amphotericin B against the pathogenic fungus Candida albicans.

机译:N-甲基-N''-十二烷基胍对两性霉素B对致病性真菌白色念珠菌的液泡靶向杀真菌活性的增强作用。

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摘要

The alkylguanidium chain attached to the polyol lactone ring of niphimycin (NM) is considered a requisite for the fungicidal activity of NM characterized by vacuole membrane fragmentation and oxidative stress induction. The addition of N-methyl-N''-dodecylguanidine to the medium can enhance the vacuole-targeting fungicidal activity of amphotericin B (AmB), in which the lactone ring has no such alkylguanidium chain, on Saccharomyces cerevisiae cells. In this study, the enhancement effect of N-methyl-N''-dodecylguanidine on the vacuole-targeting fungicidal activity of AmB was examined against Candida albicans in RPMI 1640 medium at 37 degrees C. N-methyl-N''-dodecylguanidine was lethal to C. albicans cells and additionally enhanced the vacuole disruptive activity of AmB against this pathogenic fungus. N-methyl-N''-dodecylguanidine elevated the generation of cellular reactive oxygen species when added alone in a dose-dependent manner, but its enhancement effect on AmB lethality did not accompany amplification of oxidative stress induction. The fungal vacuoles were protected against the disruptive damage even if cells were treated with H(2)O(2) alone at a lethal concentration or treated with H(2)O(2) at a sublethal concentration in combination with AmB. N-methyl-N''-dodecylguanidine was ineffective in enhancing AmB lethality or AmB-induced vacuole disruption when cells had been pretreated with ergosterol. Ergosterol-dependent mechanism is thus considered to be a possible target of N-methyl-N''-dodecylguanidine in enhancing the vacuole-targeting fungicidal activity of AmB in C. albicans cells.
机译:连接到尼霉素(NM)的多元醇内酯环上的烷基胍链被认为是以液泡膜断裂和氧化应激诱导为特征的NM杀真菌活性的必要条件。在培养基中添加N-甲基-N''-十二烷基胍可以增强两性霉素B(AmB)的液泡靶向杀真菌活性,其中内酯环不具有这样的烷基胍链,在酿酒酵母细胞上。在这项研究中,在RPMI 1640培养基中,在37摄氏度下,研究了N-甲基-N''-十二烷基胍对Amb的针对液泡的杀真菌活性的增强作用.N-甲基-N''-十二烷基胍是对白色念珠菌细胞具有致死性,并进一步增强了AmB对这种病原真菌的液泡破坏活性。当单独以剂量依赖性方式添加时,N-甲基-N''-十二烷基胍提高了细胞活性氧的产生,但是其对AmB致死性的增强作用并未伴随氧化应激诱导的放大。即使细胞单独以致死浓度的H(2)O(2)处理或以亚致死浓度的H(2)O(2)与AmB结合处理,也可以保护真菌液泡免受破坏性破坏。当用麦角固醇预处理细胞时,N-甲基-N''-十二烷基胍对增强AmB杀伤力或AmB诱导的液泡破坏无效。因此,在增强白色念珠菌细胞中AmB的液泡靶向杀真菌活性中,麦角固醇依赖性机制被认为是N-甲基-N''-十二烷基胍的可能靶标。

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