Botros Sanaa, Mahmoud Madiha, Hammam Olfat, Salah Faten, Zidek Zdenek, Masek Karel
Department of Pharmacology, Theodor Bilharz Research Institute, Warrak El-Hadar, Imbaba, Giza, Egypt.
APMIS. 2006 Jul-Aug;114(7-8):480-91. doi: 10.1111/j.1600-0463.2006.apm_380.x.
This work investigated the possible use of AdDP as adjuvant therapy to praziquantel (PZQ) in mice infected with PZQ-insusceptible Schistosoma mansoni isolate in a trial to increase the susceptibility of this isolate to the drug. Two batches of C57 BL/6 mice were infected with PZQ-susceptible and -insusceptible S. mansoni isolates, and each batch was divided into five groups. Seven weeks postinfection, the experimental group received AdDP (5 mg/kg) in addition to PZQ in reduced dose (3x100 mg/kg). Three of the remaining four groups were treated controls; they received AdDP, PZQ in reduced dose and in full dose (2x500 mg/kg), and the fourth group was infected untreated. In mice infected with PZQ-susceptible or -insusceptible S. mansoni isolate, praziquantel alone, and in addition to AdDP, reduced worm and egg loads and increased percentage dead eggs. Also, they improved the histopathological changes (reduction in granuloma diameter, percentage fibrotic area with increased percentage degenerated eggs). Inducible nitric oxide synthase (iNOS), nitric oxide (NO) in culture of peritoneal macrophages, and number of CD68-positive cells were decreased with improved alanine amino transaminase. In mice receiving combined therapy AdDP+PZQ, the antischistosomal efficacy and the reductions in the inflammatory granulomatous reactions, NO in cultured peritoneal macrophages, percentage fibrotic areas recorded, were comparable to that in mice receiving full dose of PZQ, with significantly higher reduction in CD68 cells denoting enhanced antischistosomal efficacy and healing of the inflammatory reactions in the liver.
本研究探讨了在感染对吡喹酮(PZQ)不敏感的曼氏血吸虫分离株的小鼠中,将AdDP用作PZQ辅助治疗的可能性,以提高该分离株对药物的敏感性。将两批C57 BL/6小鼠分别感染对PZQ敏感和不敏感的曼氏血吸虫分离株,每批再分为五组。感染7周后,实验组除接受降低剂量(3×100 mg/kg)的PZQ外,还接受AdDP(5 mg/kg)。其余四组中的三组为治疗对照组,分别接受AdDP、降低剂量和全剂量(2×500 mg/kg)的PZQ,第四组为未治疗的感染组。在感染对PZQ敏感或不敏感的曼氏血吸虫分离株的小鼠中,单独使用PZQ以及联合AdDP均可减少虫体和虫卵数量,并增加死卵百分比。此外,它们还改善了组织病理学变化(肉芽肿直径减小、纤维化面积百分比降低,同时退化虫卵百分比增加)。诱导型一氧化氮合酶(iNOS)、腹膜巨噬细胞培养物中的一氧化氮(NO)以及CD68阳性细胞数量减少,同时丙氨酸氨基转移酶水平改善。在接受AdDP+PZQ联合治疗的小鼠中,抗血吸虫疗效以及炎症性肉芽肿反应、培养的腹膜巨噬细胞中的NO、记录的纤维化面积百分比的降低情况,与接受全剂量PZQ的小鼠相当,CD68细胞减少更为显著,表明抗血吸虫疗效增强以及肝脏炎症反应得到改善。