El Shenawy Nahla S, Soliman Maha F M, Reyad Shimaa I
Zoology Department, Faculty of Science, Suez Canal University, Ismailia, Egypt.
Rev Inst Med Trop Sao Paulo. 2008 Jan-Feb;50(1):29-36. doi: 10.1590/s0036-46652008000100007.
The aim of this study was to assess the antioxidant and anti-schistosomal activities of the garlic extract (AGE) and Nigella sativa oil (NSO) on normal and Schistosoma mansoni-infected mice. AGE (125 mg kg-1, i.p.) and NSO (0.2 mg kg-1, i.p.) were administrated separately or in combination for successive 28 days, starting from the 1st day post infection (pi). All mice were sacrificed at weeks 7 pi. Hematological and biochemical parameters including liver and kidney functions were measured to assess the progress of anemia, and the possibility of the tissue damage. Serum total protein level, albumin, globulin and cholesterol were also determined. Malondialdehyde (MDA) and glutathione (GSH) levels were determined in the liver tissues as biomarkers for oxidative and reducing status, respectively. The possible effect of the treatment regimens on Schistosoma worms was evaluated by recording percentage of the recovered worms, tissue egg and oogram pattern. Result showed that, protection with AGE and NSO prevented most of the hematological and biochemical changes and markedly improved the antioxidant capacity of schistosomiasis mice compared to the infected-untreated ones. In addition, remarkable reduction in worms, tissue eggs and alteration in oogram pattern were recorded in all the treated groups. The antioxidant and antischistosomal action of AGE and NSO was greatly diverse according to treatment regimens. These data point to these compounds as promising agents to complement schistosomiasis specific treatment.
本研究旨在评估大蒜提取物(AGE)和黑种草籽油(NSO)对正常及感染曼氏血吸虫的小鼠的抗氧化和抗血吸虫活性。从感染后第1天起,连续28天分别或联合给予AGE(125 mg kg-1,腹腔注射)和NSO(0.2 mg kg-1,腹腔注射)。在感染后第7周处死所有小鼠。测量包括肝功能和肾功能在内的血液学和生化参数,以评估贫血进展及组织损伤的可能性。还测定了血清总蛋白水平、白蛋白、球蛋白和胆固醇。分别测定肝组织中丙二醛(MDA)和谷胱甘肽(GSH)水平,作为氧化和还原状态的生物标志物。通过记录回收蠕虫的百分比、组织虫卵和虫卵图谱模式,评估治疗方案对血吸虫的可能影响。结果表明,与未治疗的感染小鼠相比,AGE和NSO的保护作用预防了大多数血液学和生化变化,并显著提高了血吸虫病小鼠的抗氧化能力。此外,所有治疗组的蠕虫、组织虫卵数量均显著减少,虫卵图谱模式发生改变。AGE和NSO的抗氧化和抗血吸虫作用因治疗方案而异。这些数据表明这些化合物有望作为补充血吸虫病特异性治疗的药物。