首页> 外文期刊>Journal of Medical Microbiology: An Official Journal of the Pathological Society of Great Britain and Ireland >In vitro antifungal activities of amphotericin B in combination with acteoside, a phenylethanoid glycoside from Colebrookea oppositifolia
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In vitro antifungal activities of amphotericin B in combination with acteoside, a phenylethanoid glycoside from Colebrookea oppositifolia

机译:两性霉素B的体外抗真菌活性与鬼臼乙叉甙(一种来自Colebrookea oppositifolia的苯基乙醛糖苷)结合

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This study was undertaken to investigate the synergistic interaction between amphotericin B (AmB) and acteoside, isolated from the aerial parts of the shrub Colebrookea oppositifolia (Lamiaceae). Acteoside alone exhibited no intrinsic antifungal activity but showed a potent synergism in combination with AmB against selected pathogenic species, with fractional inhibitory concentration indices in the range of 0.0312–0.1562. The combination of acteoside at 3.12 and 12.5 μg ml–1 with subinhibitory concentrations of AmB resulted in a potent fungicidal effect and also exhibited a significantly extended post-antifungal effect. Furthermore, the combination also reduced the minimum biofilm reduction concentration values of AmB (2–16-fold) in preformed biofilms of Candida albicans, Cryptococcus neoformans and Aspergillus fumigatus. There was decreased viability of the cells, increased uptake of propidium iodide and enhanced leakage of 260 nm-absorbing material by Candida albicans cells when exposed to AmB in the presence of acteoside. The reason for potentiation is likely to be that the subinhibitory concentrations of AmB facilitated the uptake of acteoside, which resulted in increased killing of the fungal cells. Administration of acteoside in mice at up to 2000 mg (kg body weight)?1 by the intraperitoneal or oral route produced no overt toxicity. The data presented here support synergism between acteoside and AmB, and it is therefore proposed that a prospective new management strategy for therapeutic application of this combination should be explored.
机译:这项研究旨在调查两性霉素B(AmB)与从灌木灌木油菜科(Laceaceae)的空中部分分离出的Acteoside之间的协同相互作用。单独的Acteoside没有表现出固有的抗真菌活性,但与AmB联合使用对选定的病原体表现出有效的协同作用,分数抑制浓度指数范围为0.0312-0.1562。 3.12和12.5μgml–1的Acteoside与亚抑制浓度的AmB的结合产生有效的杀真菌作用,并且还表现出明显的抗真菌后作用。此外,该组合还降低了白色念珠菌,新型隐球菌和烟曲霉的预先形成的生物膜中AmB的最小生物膜还原浓度值(2-16倍)。当暴露于Acteoside时,白色念珠菌细胞降低了细胞的活力,增加了碘化丙啶的摄取并增强了260 nm吸收材料的泄漏。增强的原因可能是亚抑制浓度的AmB促进了藻糖苷的摄取,从而导致真菌细胞的杀伤力增加。通过腹膜内或口服途径以高达2000 mg(kg体重)?1的剂量向小鼠施用糖苷甙不会产生明显的毒性。此处提供的数据支持阿糖胞苷和AmB之间的协同作用,因此建议针对该组合的治疗应用探索一种前瞻性的新治疗策略。

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