El-Sayad Mona, Abu Helw Sahar, El-Taweel Hend, Aziz Mohammad
Dept. of Parasitology, Medical Research Institute, Alexandria University, Alexandria, Egypt.
Iran J Parasitol. 2017 Jul-Sep;12(3):446-452.
The development of new antischistosomal drug remains a pressing need and a vital challenge in front of many researchers through screening the natural or chemical substances for their potential activity as antischistosomal agents.
Five groups of -infected mice (n=10) were enrolled in this study, the G1 was infected non-treated control group. G2 was infected treated with praziquantel 500 mg/kg for 2 consecutive days. G3 was given mirazid 500 mg/kg for 5 days. G4 was given Myrrh total oil 18 mg/kg for 3 days and G5 given nitazoxanide 100 mg/kg for 7 days. Mice perfusion was performed for worm ultrastructural morphology by scanning electron microscopy at 2 WPT.
Praziquantel was superior to any other tested substances as it caused extensive tegumental damages in male worms in the form of rupture of the tubercles and loss of spines followed by mirazid that resulted only in superficial tegumental damage with shrinkage of the outer surface of male tubercles with marked loss of spines. Nitazoxanide resulted in minor tegumental alterations of male worms while Myrrh total oil caused negligible effects on the teguments of perfused worms.
PZQ showed more superior antiparasitic effects than all tested substances on worms. Mirazid was more effective than myrrh total oil and nitazoxanide.
通过筛选天然或化学物质作为抗血吸虫药物的潜在活性,开发新型抗血吸虫药物仍然是许多研究人员面临的迫切需求和重大挑战。
本研究纳入五组感染小鼠(n = 10),G1组为感染未治疗对照组。G2组感染后连续2天用吡喹酮500mg/kg治疗。G3组给予米拉齐德500mg/kg,持续5天。G4组给予没药总油18mg/kg,持续3天,G5组给予硝唑尼特100mg/kg,持续7天。在感染后2周通过扫描电子显微镜对小鼠进行灌注以观察虫体超微结构形态。
吡喹酮优于任何其他受试物质,因为它导致雄虫体表广泛损伤,表现为结节破裂和棘突丧失,其次是米拉齐德,其仅导致体表轻微损伤,雄虫结节外表面收缩,棘突明显丧失。硝唑尼特导致雄虫体表轻微改变,而没药总油对灌注虫体的体表影响可忽略不计。
吡喹酮对虫体的抗寄生虫作用比所有受试物质更优越。米拉齐德比没药总油和硝唑尼特更有效。