Haynes M P, Buckley H R, Higgins M L, Pieringer R A
Department of Biochemistry, Fels Institute for Cancer Research and Molecular Biology, Temple University School of Medicine, Philadelphia, Pennsylvania 19140.
Antimicrob Agents Chemother. 1994 Jul;38(7):1523-9. doi: 10.1128/AAC.38.7.1523.
The alkyl glycerol ether rac-1-O-dodecylglycerol inhibited the growth of members of two genera of yeasts, Candida and Cryptococcus, and was strongly synergistic with amphotericin B. At one-half its MIC, dodecylglycerol decreased the MIC of amphotericin B by as much as 80-fold. This high degree of synergism between dodecylglycerol and amphotericin B was demonstrated against a number of species of yeasts including Candida albicans, Candida tropicalis, Candida parapsilosis, Cryptococcus neoformans, Cryptococcus albidus, and Cryptococcus laurentii. All fractional inhibitory concentrations (for all strains and species) were calculated to be less than 1, and most were less than 0.6, again demonstrating strong synergism. Other alkyl glycerol ethers with alkyl chain lengths ranging from 8 to 18 carbon atoms were also found to be synergistic with amphotericin B against C. neoformans and C. albicans. Electron microscopy experiments showed that C. neoformans grown in the presence of dodecylglycerol had severely abnormal, deformed capsules. Although the mechanism of action of dodecylglycerol is not known, dodecylglycerol was not simply acting as a detergent. The natural detergent sodium deoxycholate could not substitute for dodecylglycerol. At comparable and higher concentrations, sodium deoxycholate had no fungicidal effect on its own, nor did it potentiate the activity of amphotericin B. Dodecylglycerol did not interact synergistically with the water-soluble antifungal agent fluconazole. The lipid-soluble hydrophobic properties of amphotericin B appear to be important for this synergistic effect, in that alkyl glycerol ethers could promote synergism with amphotericin B by potentially increasing the interaction between membrane-bound ergosterol and amphotericin B.
烷基甘油醚外消旋-1-O-十二烷基甘油抑制了念珠菌属和隐球菌属这两个酵母属成员的生长,并且与两性霉素B具有强烈的协同作用。在其最低抑菌浓度(MIC)的一半时,十二烷基甘油可将两性霉素B的MIC降低多达80倍。十二烷基甘油与两性霉素B之间的这种高度协同作用在多种酵母菌种中得到了证实,包括白色念珠菌、热带念珠菌、近平滑念珠菌、新生隐球菌、浅白隐球菌和罗伦隐球菌。所有的部分抑菌浓度(针对所有菌株和菌种)经计算均小于1,且大多数小于0.6,再次证明了强烈的协同作用。还发现其他烷基链长度在8至18个碳原子之间的烷基甘油醚与两性霉素B对新生隐球菌和白色念珠菌具有协同作用。电子显微镜实验表明,在十二烷基甘油存在下生长的新生隐球菌具有严重异常、变形的荚膜。尽管十二烷基甘油的作用机制尚不清楚,但它并非仅仅起到去污剂的作用。天然去污剂脱氧胆酸钠不能替代十二烷基甘油。在相当及更高浓度下,脱氧胆酸钠自身没有杀菌作用,也不能增强两性霉素B的活性。十二烷基甘油与水溶性抗真菌剂氟康唑没有协同相互作用。两性霉素B的脂溶性疏水特性对于这种协同作用似乎很重要,因为烷基甘油醚可能通过潜在地增加膜结合麦角甾醇与两性霉素B之间的相互作用来促进与两性霉素B的协同作用。