Kobayashi Motoo, Sato Ikuko, Abe Fumie, Nitta Kumiko, Hashimoto Michizane, Fujie Akihiko, Hino Motohiro, Hori Yasuhiro
Fermentation Research Laboratories, Fujisawa Pharmaceutical Co., Ltd., 5-2-3 Tokodai, Tsukuba, Ibaraki 300-2698, Japan.
J Antibiot (Tokyo). 2004 Dec;57(12):788-96. doi: 10.7164/antibiotics.57.788.
FR227244 is a novel triterpene glycoside that exhibits in vitro antifungal activity against filamentous fungi such as Aspergillus sp. and Trichophyton sp. and yeast such as Candida utilis and Candida parapsilosis but shows low activity against Candida albicans, Candida krusei and Candida tropicalis. Specifically, FR227244 exhibits in vitro and in vivo antifungal activity against Aspergillus fumigatus. The minimum effective concentration (MEC) of FR227244 against A. fumigatus FP1305 in a micro-broth dilution test was 0.031 microg/ml. FR227244 showed good efficacy by subcutaneous injection and oral administration against A. fumigatus in a murine systemic infection model, with ED(50)s of 1.9 and 18 mg/kg, respectively. FR227244 inhibited glucan synthesis in a 1,3-beta-glucan synthase assay weakly and in whole cells strongly, but did not effect other macromolecule synthesis, including protein, nucleic acids, mannan and chitin. These results and the effect on hyphal morphology of A. fumigatus suggested that FR227244 showed antifungal activity based on inhibition of glucan synthesis.
FR227244是一种新型三萜糖苷,对丝状真菌如曲霉属和毛癣菌属以及酵母如产朊假丝酵母和近平滑假丝酵母具有体外抗真菌活性,但对白色念珠菌、克柔念珠菌和热带念珠菌的活性较低。具体而言,FR227244对烟曲霉具有体外和体内抗真菌活性。在微量肉汤稀释试验中,FR227244对烟曲霉FP1305的最低有效浓度(MEC)为0.031微克/毫升。在小鼠全身感染模型中,通过皮下注射和口服给药,FR227244对烟曲霉显示出良好的疗效,其半数有效剂量(ED50)分别为1.9和18毫克/千克。在1,3-β-葡聚糖合酶试验中,FR227244对葡聚糖合成的抑制作用较弱,但在全细胞中作用较强,且对包括蛋白质、核酸、甘露聚糖和几丁质在内的其他大分子合成没有影响。这些结果以及对烟曲霉菌丝形态的影响表明,FR227244基于对葡聚糖合成的抑制而显示出抗真菌活性。