oxiconazole与ro14 -4767/002对白色念珠菌固醇型的影响。

A Polak-Wyss, H Lengsfeld, G Oesterhelt
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引用次数: 22

摘要

研究了咪唑氧康唑及其啉衍生物Ro 14-4767/002对白色念珠菌不同生长时期甾醇代谢的影响。麦角甾醇是对照细胞的主要甾醇成分,在氧康唑处理和Ro 14-4767/002处理的细胞中显著减少。然而,两种药物处理的细胞中总甾醇含量增加,这是由于对照组细胞中不存在其他固醇的积累:在氧康唑处理的细胞中,24-甲基二氢羊毛甾醇、4,14-二甲基雌狐甾醇和14-甲基雌狐甾醇积累,表明c14 -去甲基化受到抑制。这与在各种病原体真菌中描述的其他唑的作用模式一致。在Ro 14-4767/002处理的细胞中,积累的主要甾醇是ignosterol,表明抑制了δ 14-甾醇还原酶和δ 8- δ 7-异构酶。这种抑制作用在人类病原体中还没有被描述过,尽管以前在用苯丙啉处理过的植物病原真菌中发现过。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of oxiconazole and Ro 14-4767/002 on sterol pattern in Candida albicans.

The effect of the imidazole oxiconazole and the morpholine derivative Ro 14-4767/002 on the sterol metabolism of Candida albicans was investigated at different periods of growth. Ergosterol, representing the main sterol component of control cells, was markedly reduced in oxiconazole-treated and Ro 14-4767/002-treated cells. However, the total sterol content of the cells treated with both drugs was increased due to accumulation of other sterols not present in control cells: in oxiconazole-treated cells 24-methenedihydrolanosterol, 4,14-dimethylfecosterol and 14-methylfecosterol accumulated, indicating an inhibition of C14-demethylation. This is in agreement with the mode of action described for other azoles in various pathogen fungi. In Ro 14-4767/002-treated cells the main sterol accumulated was ignosterol, indicating an inhibition of delta 14-sterol reductase and delta 8-delta 7-isomerase. This inhibition has not been described before in human pathogens although it has been previously found in plant pathogenic fungi treated with fenpropimorph.

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