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首页> 外文期刊>Phytomedicine : >β-Asarone, an active principle of Acorus calamus rhizome, inhibits morphogenesis, biofilm formation and ergosterol biosynthesis in Candida albicans
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β-Asarone, an active principle of Acorus calamus rhizome, inhibits morphogenesis, biofilm formation and ergosterol biosynthesis in Candida albicans

机译:β-asarone,Acorus calamus relizome的活跃原理,抑制了念珠菌在念珠菌的形态发生,生物膜形成和ergosterol生物合成

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摘要

Anti-Candida potential of Acorus calamus rhizome and its active principle, β-asarone, was evaluated against the human fungal pathogen, Candida albicans. β-Asarone exhibited promising growth inhibitory activity at 0.5 mg/ml and it was fungicidal at 8 mg/ml. Time dependant kill curve assay showed that MFC of β-asarone was highly toxic to C. albicans, killing 99.9% inoculum within 120 min of exposure. β-Asarone caused significant inhibition of C. albicans morphogenesis and biofilm development at sub-inhibitory concentrations. Our data indicate that the growth inhibitory activity of β-asarone might be through inhibition of ergosterol biosynthesis. Hemolytic assay showed that β-asarone is non-toxic, even at concentrations approaching MIC value. Our results suggest that β-asarone may be safe as a topical antifungal agent.
机译:抗念珠菌的抗念珠菌潜力和其活跃的原理β-砷酮,对人类真菌病原体,念珠菌念珠菌进行评估。 β-亚辛酮在0.5mg / ml下表现出有希望的生长抑制活性,并且在8mg / ml下杀菌剂是杀真菌剂。 时间依赖性杀死曲线测定表明,β-亚辛的MFC对敏感的β-醇酮毒性毒性高,在暴露的暴露中造成99.9%的接种物。 β-溶酮导致亚抑制浓度的敏感型混蛋的显着抑制和生物膜发育。 我们的数据表明,β-砷酮的生长抑制活性可能是通过抑制Ergosterol生物合成的。 溶血性测定表明,即使在接近MIC值的浓度下,β-亚辛是无毒的。 我们的研究结果表明,β-asarone可以作为局部抗真菌剂安全。

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