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Effects of squalene epoxidase inhibitors on Candida albicans.

机译:角鲨烯环氧酶抑制剂对白色念珠菌的影响。

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摘要

The relationship between sterol biosynthesis inhibition, membrane integrity, and cell growth inhibition in Candida albicans was examined for five squalene epoxidase inhibitors. The compounds were the thiocarbamates tolnaftate and tolciclate and the allylamines naftifine, terbinafine, and SDZ 87-469. All compounds inhibited sterol biosynthesis, with the concentrations that caused a 50% decrease in the total sterol-to-squalene ratio ranging from less than or equal to 0.01 microM for terbinafine and SDZ 87-469 to 500 microM for tolnaftate. At 100 microM, the compounds also caused up to a 30% release of intracellular [14C]aminoisobutyric acid. With terbinafine and SD2 87-469, aminoisobutyric acid release further increased in cells grown at concentrations that inhibited ergosterol biosynthesis. It is suggested that inhibition of ergosterol synthesis may render the C. albicans membrane susceptible to further damage, including direct damage from squalene epoxidase inhibitors.
机译:研究了五种角鲨烯环氧酶抑制剂对白色念珠菌中固醇生物合成抑制,膜完整性和细胞生长抑制之间的关系。化合物是硫代氨基甲酸酯甲苯磺酸盐和甲苯磺酸盐以及烯丙胺萘替芬,特比萘芬和SDZ 87-469。所有化合物均抑制了固醇的生物合成,其浓度导致总固醇与角鲨烯之比降低了50%,范围从特比萘芬和SDZ 87-469的小于或等于0.01 microM到甲苯磺酸酯的SDZ降至500 microM。在100 microM时,这些化合物还导致细胞内[14C]氨基异丁酸释放高达30%。使用特比萘芬和SD2 87-469,氨基异丁酸的释放在抑制麦角固醇生物合成浓度的细胞中进一步释放。建议抑制麦角固醇的合成可能使白色念珠菌膜容易受到进一步的损害,包括角鲨烯环氧酶抑制剂的直接损害。

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