de Oliveira Claudineide Nascimento Fernandes, Frezza Tarsila Ferraz, Garcia Vera Lúcia, Figueira Glyn Mara, Mendes Tiago Manuel Fernandes, Allegretti Silmara Marques
Biology Institute, Animal Biology Department, Campinas State University (UNICAMP), SP, Brazil.
Multidisciplinary Center of Chemical Biological and Agricultural Research (CPQBA), Campinas State University (UNICAMP), Paulínia, SP, Brazil.
Exp Parasitol. 2017 Dec;183:56-63. doi: 10.1016/j.exppara.2017.10.008. Epub 2017 Oct 23.
Human schistosomiasis is an important neglected tropical disease caused by blood flukes of the genus Schistosoma and is responsible for more than 280,000 deaths annually. Treatment for this disease relies currently on a single drug, praziquantel (PZQ). Concerns regarding PZQ resistance and insensitivity of juvenile schistosomes have increased the interest in resorting to medicinal plants for alternative drug therapies. This study aimed to perform an in vivo schistosomicidal activity evaluation of crude hexanic (HE) and ethanolic (EE) extracts obtained from Phyllanthus amarus in mice infected with Schistosoma mansoni (BH strain). Mice were treated orally with a single dose of 100 or 250 mg/kg, on two different infection periods, 30 and 45 days post-infection (dpi). Parameters such as worm recovery, faecal egg count, intestinal tissue egg count and liver histopathology were evaluated. Treatment against young adult (30 dpi) and adult (45 dpi) worms were more effective compared to the control group treated with PZQ. At a concentration of 250 mg/kg (30 dpi) EE showed a 54.4% female reduction and a 61.2% total worm reduction whilst at a concentration of 100 mg/kg (45 dpi) HE showed a 40.6% female worm reduction and a 45.3% total worm reduction. Histopathological examination showed a granuloma decrease in both number and size for groups treated with 250 mg/kg of HE (45 dpi) or EE (30 or 45 dpi). From these results, it can be concluded that both hexanic and ethanolic extracts have antischistosomal activities, however, act differently according to the parasites age. The schistosomicidal activity results in groups treated 30 days post infection is extremely important since praziquantel does not show activity against the juvenile forms of Schistosoma.
人类血吸虫病是一种由血吸虫属的血吸虫引起的重要的被忽视的热带病,每年导致超过28万人死亡。目前,这种疾病的治疗依赖于单一药物吡喹酮(PZQ)。对吡喹酮耐药性以及幼年血吸虫不敏感性的担忧,增加了人们对采用药用植物进行替代药物治疗的兴趣。本研究旨在对从苦味叶下珠中获得的正己烷提取物(HE)和乙醇提取物(EE)在感染曼氏血吸虫(BH株)的小鼠体内进行杀血吸虫活性评估。在感染后的两个不同时期,即感染后30天和45天,给小鼠口服单剂量100或250mg/kg的提取物。评估了诸如虫体回收率、粪便虫卵计数、肠组织虫卵计数和肝脏组织病理学等参数。与用吡喹酮治疗的对照组相比,针对年轻成虫(感染后30天)和成虫(感染后45天)的治疗更有效。在250mg/kg(感染后30天)的浓度下,EE显示雌虫减少54.4%,总虫体减少61.2%,而在100mg/kg(感染后45天)的浓度下,HE显示雌虫减少40.6%,总虫体减少45.3%。组织病理学检查显示,用250mg/kg的HE(感染后45天)或EE(感染后30天或45天)治疗的组中肉芽肿的数量和大小均减少。从这些结果可以得出结论,正己烷提取物和乙醇提取物都具有抗血吸虫活性,然而,根据寄生虫的年龄作用方式不同。感染后30天治疗组的杀血吸虫活性结果极其重要,因为吡喹酮对血吸虫的幼年形式没有活性。