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奥昔康唑和Ro 14 - 4767/002对白色念珠菌甾醇模式的影响。

Effect of oxiconazole and Ro 14-4767/002 on sterol pattern in Candida albicans.

作者信息

Polak-Wyss A, Lengsfeld H, Oesterhelt G

出版信息

Sabouraudia. 1985 Dec;23(6):433-41. doi: 10.1080/00362178585380631.

Abstract

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.

摘要

在不同生长阶段研究了咪唑氧康唑和吗啉衍生物Ro 14-4767/002对白色念珠菌甾醇代谢的影响。麦角甾醇是对照细胞的主要甾醇成分,在氧康唑处理的细胞和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,这是由于对照细胞中不存在的其他甾醇积累所致:在氧康唑处理的细胞中,24-亚甲基二氢羊毛甾醇、4,14-二甲基麦角甾醇和14-甲基麦角甾醇积累,表明C14-去甲基化受到抑制。这与各种致病真菌中其他唑类的作用模式一致。在Ro 14-4767/002处理的细胞中积累的主要甾醇是羊毛甾醇,表明δ14-甾醇还原酶和δ8-δ7-异构酶受到抑制。尽管之前在用粉唑醇处理的植物致病真菌中发现过这种抑制作用,但在人类病原体中尚未有过相关描述。

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