El-Sayed Nagwa Mostafa
Medical Parasitology Department, Research Institute of Ophthalmology, Ministry of Scientific Research and Technology, Giza, Egypt.
J Parasit Dis. 2017 Dec;41(4):1020-1027. doi: 10.1007/s12639-017-0928-0. Epub 2017 May 22.
This study evaluated the effect of e (e) ethanol extract on the viability, embryogenesis and infectivity () eggs. It was carried out both in vitro and in vivo. In the in vitro experiment, unembryonated eggs were incubated with 25, 50 and 100 mg/mL e extract at 25 °C for 6, 12, and 24 h to assess the effect of e on their viability and for two weeks to assess the effect of e on their embryogenesis. In vivo experiment was performed to assess the effect of e on infectivity of eggs. Treated embryonated eggs by extract at concentrations of 25, 50 and 100 mg/mL for 24 h were inoculated into mice and their livers were examined for the presence of larvae on the 7th day after infection and for histopathological evaluation at 14th day post-infection. e showed a significant ovicidal activity on eggs. The best effect was observed with 100 mg/mL concentration after 24 h with an efficacy of 98.2%. However, the treated eggs by 25, 50 mg/mL of extract after 24 h showed ovicidal activity by 59.22 and 82.5% respectively. Moreover, this extract effectively inhibited eggs embryogenesis by 99.64% and caused their degeneration at the concentration of 100 mg/mL after 2 weeks of treatment. However, the lower concentrations, 25 and 50 mg/mL inhibited embryogenesis by 51.19 and 78.57% respectively. The effect of e on the infectivity eggs was proven by the reduction of larvae recovery in the livers by 35.9, 62.8 and 89.5% in mice groups inoculated by treated eggs at concentrations of 25, 50 and 100 mg/mL respectively. Histopathologically, the liver tissues of mice infected with treated eggs at the concentration of 100 mg/mL appeared healthy with slight degenerative changes of hepatocytes, opposite to that recorded in the infected mice with treated eggs by the lower concentrations. In conclusion; extract possessed dose-dependent anti- activity on the viability, embryogenesis and infectivity of eggs.
本研究评估了[提取物名称]乙醇提取物对[寄生虫名称]虫卵活力、胚胎发育及感染性的影响。研究在体外和体内环境中均有开展。在体外实验中,未受精的[寄生虫名称]虫卵于25℃下分别与浓度为25、50和100mg/mL的[提取物名称]提取物孵育6、12和24小时,以评估该提取物对虫卵活力的影响;并孵育两周以评估其对虫卵胚胎发育的影响。体内实验旨在评估[提取物名称]对[寄生虫名称]虫卵感染性的影响。将经浓度为25、50和100mg/mL的[提取物名称]提取物处理24小时的受精虫卵接种到小鼠体内,并在感染后第7天检查小鼠肝脏中是否存在[寄生虫名称]幼虫,在感染后第14天进行组织病理学评估。[提取物名称]对[寄生虫名称]虫卵显示出显著的杀卵活性。24小时后,100mg/mL浓度组效果最佳,杀卵率达98.2%。然而,24小时后,25mg/mL和50mg/mL浓度的[提取物名称]提取物处理组的杀卵率分别为59.22%和82.5%。此外,该提取物在处理两周后,在100mg/mL浓度下可有效抑制[寄生虫名称]虫卵胚胎发育达99.64%,并导致虫卵退化。不过,25mg/mL和50mg/mL的较低浓度分别抑制胚胎发育51.19%和78.57%。通过分别接种经25、50和100mg/mL浓度的[提取物名称]提取物处理的虫卵的小鼠组肝脏中幼虫回收率降低35.9%、62.8%和89.5%,证明了[提取物名称]对[寄生虫名称]虫卵感染性的影响。组织病理学上,感染经100mg/mL浓度的[提取物名称]提取物处理的虫卵的小鼠肝脏组织看起来健康,肝细胞仅有轻微退行性变化,这与感染经较低浓度提取物处理的虫卵的小鼠情况相反。总之,[提取物名称]提取物对[寄生虫名称]虫卵的活力、胚胎发育及感染性具有剂量依赖性的抗[寄生虫名称]活性。