Morsy Nagy, Houdai Toshihiro, Konoki Keiichi, Matsumori Nobuaki, Oishi Tohru, Murata Michio
Department of Chemistry, Graduate School of Science, Osaka University, 1-16 Machikaneyama, Toyonaka, Osaka 560-0043, Japan.
Bioorg Med Chem. 2008 Mar 15;16(6):3084-90. doi: 10.1016/j.bmc.2007.12.029. Epub 2007 Dec 23.
Amphidinols (AMs) are a new class of polyhydroxyl polyene compounds with potent antifungal activity. Membrane-permeabilizing activities of AM2, AM3, and AM6 were examined using fluorescent-dye leakage experiments with various phosphatidylcholines (PCs) and sterols. All the AMs tested showed the potent activity to cholesterol-containing liposomes. In the absence of the sterol, AM2, AM3, and AM6 had no membrane-permeabilizing activities to membranes of saturated PC. In liposomes consisting of unsaturated PC, AM2, which possesses an additional ether ring in a polyhydroxyl chain, showed membrane-permeabilizing activities with a moderate efficacy, while AM3 or AM6 did not. The potentiation by sterols was prominent even at 0.5% (wt/wt) and structure-dependent, which ruled out the possibility that alteration of the membrane physical properties induced by sterol was chiefly responsible for this sterol effect. The finding that their activity was not affected by membrane thickness implies that AMs permeabilized membrane by a different mechanism from that of polyene macrolide antibiotics.
两性霉素(AMs)是一类新型的具有强大抗真菌活性的多羟基多烯化合物。使用各种磷脂酰胆碱(PCs)和甾醇进行荧光染料泄漏实验,研究了AM2、AM3和AM6的膜通透活性。所有测试的AMs对含胆固醇的脂质体均表现出强大活性。在没有甾醇的情况下,AM2、AM3和AM6对饱和PC膜没有膜通透活性。在由不饱和PC组成的脂质体中,在多羟基链中具有额外醚环的AM2表现出中等效力的膜通透活性,而AM3或AM6则没有。即使在0.5%(重量/重量)时,甾醇的增强作用也很显著且具有结构依赖性,这排除了甾醇引起的膜物理性质改变是这种甾醇效应主要原因的可能性。它们的活性不受膜厚度影响这一发现表明,AMs通过与多烯大环内酯类抗生素不同的机制使膜通透。