Zoology Department, Faculty of Science, Menufiya University, Egypt.
Molecular Biology Department, Genetic Engineering and Biotechnology Institute, Sadat City University, Egypt.
Exp Parasitol. 2014 Oct;145:7-13. doi: 10.1016/j.exppara.2014.06.016. Epub 2014 Jul 10.
This study aims to evaluate the immunomodulatory effects of a natural product, blue green algae (BGA) (100 mg/kg BW), alone or combined with praziquantel PZQ (250 mg/kg BW) on granulomatous inflammation, liver histopathology, some biochemical and immunological parameters in mice infected with Schistosoma mansoni. Results showed that the diameter and number of egg granuloma were significantly reduced after treatment of S. mansoni-infected mice with BGA, PZQ and their combination. The histopathological alterations observed in the liver of S. mansoni-infected mice were remarkably inhibited after BGA treatments. BGA decreased the activities of aspartate aminotransferase (AST), alanine aminotransferase (ALT) and alkaline phosphatase (ALP) as well as the level of total protein (TP) while the level of albumin was increased. Treatment of infected mice with BGA, PZQ as well as their combination led to significant elevation in the activities of hepatic antioxidant enzymes glutathione peroxidase (GPX) and glutathione-S-transferase (GST) as compared with control group. Combination of BGA and PZQ resulted in significant reduction in the level of intercellular adhesion molecules-1 (ICAM-1), vascular adhesion molecules-1 (VCAM-1) and tumor necrosis factor-alpha (TNF-α) when compared to those of the S. mansoni-infected group. Overall, BGA significantly inhibited the liver damage accompanied with schistosomiasis, exhibited a potent antioxidant and immunoprotective activities. This study suggests that BGA can be considered as promising for development a complementary and/or alternative medicine against schistosomiasis.
本研究旨在评估一种天然产物——蓝绿藻(BGA)(100mg/kgBW)单独或与吡喹酮(PZQ)(250mg/kgBW)联合对曼氏血吸虫感染小鼠的肉芽肿炎症、肝组织病理学、一些生化和免疫参数的免疫调节作用。结果表明,BGA、PZQ 及其联合治疗曼氏血吸虫感染小鼠后,卵肉芽肿的直径和数量显著减少。BGA 处理可显著抑制曼氏血吸虫感染小鼠肝脏的组织病理学改变。BGA 降低了天冬氨酸氨基转移酶(AST)、丙氨酸氨基转移酶(ALT)和碱性磷酸酶(ALP)的活性以及总蛋白(TP)水平,同时白蛋白水平升高。与对照组相比,BGA、PZQ 以及它们的联合治疗使感染小鼠的肝抗氧化酶谷胱甘肽过氧化物酶(GPX)和谷胱甘肽-S-转移酶(GST)的活性显著升高。与曼氏血吸虫感染组相比,BGA 和 PZQ 的联合治疗使细胞间黏附分子-1(ICAM-1)、血管细胞黏附分子-1(VCAM-1)和肿瘤坏死因子-α(TNF-α)的水平显著降低。总之,BGA 显著抑制了伴有血吸虫病的肝损伤,表现出强大的抗氧化和免疫保护活性。本研究表明,BGA 可被认为是一种有前途的抗血吸虫病的补充和/或替代药物。