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Therapeutic effect of alpha lipoic acid combined with praziquantel on liver fibrosis induced by Schistosoma mansoni challenged mice

机译:α硫辛酸联合吡喹酮对曼氏血吸虫攻击小鼠肝纤维化的治疗作用

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Schistosomiasis is an endemic disease in 74 countries causing more than 250,000 deaths every year. Accordingly, the development of an effective drug for eradication of schistosomiasis is an open research field. The current chemotherapy for control is praziquantel (PZQ). However, PZQ does not improve liver fibrosis. Therefore, the aim of this study is to evaluate the combined effect of alpha lipoic acid (ALA) with PZQ on the liver fibrosis induced by Schistosoma mansoni challenged mice. Evaluation was based on the worm burden count, ova load, granuloma size, and histopathology of the liver. Reduced glutathione (GSH) was measured in the tissue as a biomarker for impaired antioxidant function. Malondialdehyde (MDA) was also measured in the tissue as a biomarker for oxidative stress. The serum level of matrix metalloproteinase 1 was measured as a biomarker for fibrotic status of the liver. Liver function enzymes such as ALT, AST, and GGT were also measured. Four groups of ten mice each were used in this study. The first group was infected with 50±10 S. mansoni cercariae. The second group was also infected and was treated with PZQ 9 weeks post-infection (PI). The third group was treated with PZQ and ALA 9 weeks PI. The fourth group was used a healthy control. The present study revealed remarkable improvement in all parameters measured (parasitological and biochemical) as well as significant improvement of hepatic pathology in the third group which was treated with PZQ and ALA. The treatment of mice with PZQ and ALA results in reduction in the worm burden, egg count, and granuloma size. Furthermore, this combined treatment increased the tissue level of the antioxidant (GSH) and decreased the tissue level of MDA in this group.
机译:血吸虫病是74个国家/地区的地方病,每年造成25万多人死亡。因此,开发消灭血吸虫病的有效药物是一个开放的研究领域。当前用于控制的化疗是吡喹酮(PZQ)。但是,PZQ不能改善肝纤维化。因此,本研究的目的是评估α硫辛酸(ALA)和PZQ对曼氏血吸虫感染小鼠肝纤维化的联合作用。评估基于蠕虫负荷计数,卵子负荷,肉芽肿大小和肝脏的组织病理学。在组织中测出还原型谷胱甘肽(GSH)作为抗氧化功能受损的生物标志物。丙二醛(MDA)在组织中也被测量为氧化应激的生物标记。测量基质金属蛋白酶1的血清水平作为肝脏纤维化状态的生物标志物。还测量了肝功能酶,例如ALT,AST和GGT。在该研究中使用四组,每组十只小鼠。第一组感染了50±10曼氏葡萄球菌。第二组也被感染,并在感染后(PI)9周接受PZQ治疗。第三组接受PZQ和ALA治疗PI 9周。第四组用作健康对照。本研究显示,第三组接受PZQ和ALA治疗的所有参数(寄生虫学和生化指标)均显着改善,肝病理学也显着改善。用PZQ和ALA治疗小鼠可减少蠕虫负担,卵数和肉芽肿大小。此外,在该组中,这种联合治疗增加了抗氧化剂(GSH)的组织水平,并降低了MDA的组织水平。

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