摘要
目的 为抗真菌药物作用机理的研究提供有力的工具。方法 白念珠菌经药物作用后提取未皂化脂 (NSLs) ,其中的甾醇组分经衍生化后GC MS分析 ,测定各组分的结构和含量。结果 经氟康唑作用的真菌 ,CYP5 1酶受抑制 ,使细胞膜内羊毛甾醇和2 4 (2 8) 亚甲基 2 4 ,2 5 二氢羊毛甾醇累积 ,后者更为明显 ,而麦角甾醇合成受阻。结论GC MS分析获满意的效果 ,可对抗真菌药物阻断真菌麦角甾醇合成通路所引起各甾醇组分的含量变化进行研究。
AIM To provide an effective method for studying the mechanism of pharmacological effects of antifungal agents. METHODS From Candida albicans treated with fluconazole(inhibitor of ergosterol biosynthesis), the nonsaponifiable lipids (NSLs) were extracted and the sterol components of NSLs were separated and analyzed as their N trimethylsilylimidazole derivatives by gas chromatography mass spectrometry(GC MS). RESULTS Ergosterol was the predominant component of NSLs in control cells but showed a progressive decline during treatment with fluconazole. CYP51 was inhibited, while the lanosterol and trimethyl(24 methylenelanost 8 en 3 ol) were accumulated to high levels, the later was seen more significantly. CONCLUSION The satisfactory results are obtained by GC MS analysis and it can be used to study the inhibition of antifungal agents on sterol biosynthesis with the shift in sterol composition.
出处
《中国药理学与毒理学杂志》
CAS
CSCD
北大核心
2002年第5期368-371,共4页
Chinese Journal of Pharmacology and Toxicology
基金
国家自然科学基金资助项目 (39770 876 )
上海市科技发展基金资助项目 (98QB14 0 0 9)
