Bioactive Natural Products Laboratory, Department of Biochemistry, Institute of Biological Sciences, Federal University of Juiz de Fora, 36036 900 Juiz de Fora, MG, Brazil.
Schistosomiasis Laboratory, René Rachou Research Center, FIOCRUZ, 30190 002 Belo Horizonte, MG, Brazil.
Biomed Res Int. 2014;2014:941318. doi: 10.1155/2014/941318. Epub 2014 May 8.
The aims of this work were to evaluate the in vitro and in vivo schistosomicidal properties of the methanolic extract of the aerial parts of Mitracarpus frigidus (MFM) and to determine its HPLC profile. For the in vitro experiment, four pairs of adult worms, obtained from infected mice, were exposed to different concentrations of MFM (100 to 400 μg/mL) for 24 and 48 h and analyzed under an inverted microscope. For the in vivo experiment, mice were inoculated with cercariae and, 20 days after infection, MFM (100 and 300 mg/kg) was administered orally for the following 25 days. Mice were euthanized after 60 days. MFM showed in vitro schistosomicidal activity, exhibiting the opening of the gynaecophoral canal of some male schistosomes, the presence of contorted muscles, vesicles, and the darkening of the paired worms skin. In vivo experiments showed that MFM treatments significantly reduced total worm count, as praziquantel, showing a decrease in liver and spleen weight. Also, a significant reduction in granuloma density was observed. MFM treatment did not cause alterations in the liver function of either infected or noninfected mice. The HPLC chromatogram profile showed the presence of kaempferol-O-rutinoside, rutin, kaempferol, psychorubrin, and ursolic acid.
本研究旨在评估 Mitracarpus frigidus(MFM)地上部分甲醇提取物的体内外杀血吸虫活性,并确定其 HPLC 图谱。在体外实验中,将从感染小鼠中获得的四对成虫在不同浓度的 MFM(100 至 400μg/mL)中暴露 24 和 48 小时,并在倒置显微镜下进行分析。在体内实验中,用尾蚴接种小鼠,感染后 20 天,用 MFM(100 和 300mg/kg)口服给药 25 天。感染 60 天后处死小鼠。MFM 表现出体外杀血吸虫活性,导致一些雄性血吸虫的生殖腔开口,肌肉扭曲,出现囊泡,以及配对蠕虫皮肤变黑。体内实验表明,MFM 治疗可显著降低总虫数,与吡喹酮相当,肝脾重量也有所减轻。此外,还观察到肉芽肿密度显著降低。MFM 治疗未引起感染或未感染小鼠肝功能改变。HPLC 色谱图显示存在山奈酚-O-芸香糖苷、芦丁、山奈酚、psychorubrin 和熊果酸。