Jarusiewicz Jamie A, Sherma Joseph, Fried Bernard
Department of Chemistry, Lafayette College, Easton, PA 18042, USA.
Comp Biochem Physiol B Biochem Mol Biol. 2006 Nov-Dec;145(3-4):346-9. doi: 10.1016/j.cbpb.2006.08.008. Epub 2006 Sep 3.
Thin layer chromatography was used to analyze the glucose and maltose concentrations of the digestive gland-gonad complex (DGG) of uninfected-estivated Biomphalaria glabrata snails and estivated B. glabrata patently infected with Schistosoma mansoni. All snails were estivated in a most chamber at a relative humidity of 98+/-1% and a temperature of 23+/-1 degrees C for 14 days. Carbohydrates were extracted from the DGG with 70% aqueous ethanol, and extracts were analyzed on silica gel preadsorbent plates using ethyl acetate-glacial acetic acid-methanol-water (60:15:15:10) mobile phase, alpha-naphthol-sulfuric acid detection reagent, and quantification by densitometry. The concentrations of glucose and maltose were significantly reduced in both uninfected-estivated snails and infected-estivated snails.
采用薄层色谱法分析未感染且处于夏眠状态的光滑双脐螺以及明显感染曼氏血吸虫且处于夏眠状态的光滑双脐螺消化腺-性腺复合体(DGG)中的葡萄糖和麦芽糖浓度。所有螺均在湿度为98±1%、温度为23±1摄氏度的最适环境中夏眠14天。用70%乙醇水溶液从DGG中提取碳水化合物,提取物在硅胶预吸附板上进行分析,使用乙酸乙酯-冰醋酸-甲醇-水(60:15:15:10)流动相、α-萘酚-硫酸检测试剂,并通过光密度法进行定量。未感染且处于夏眠状态的螺以及感染且处于夏眠状态的螺中葡萄糖和麦芽糖的浓度均显著降低。