Attallah A M, Wahba M A, Elsheikha H M, Abbas A T, Abdel Aziz M M, El-Hemaly M A
Research and Development Department, Biotechnology Research Center, New Damietta City, Egypt.
Parasitol Res. 2008 Aug;103(3):567-76. doi: 10.1007/s00436-008-1011-7. Epub 2008 May 31.
The present study tested the hypothesis that mice exposed to Schistosoma mansoni and treated with the insecticide Larvin have an increased risk of accelerated liver damage. To investigate this hypothesis, adverse effects resulting from treatment with Larvin were compared between S. mansoni-exposed and nonexposed outbred albino mice. The effects of concurrent treatment with Larvin on the progress and outcomes of S. mansoni infection were assessed via macroscopic and microscopic examination of liver and spleen, evaluation of several hematological, biochemical and hepatic enzymes parameters, and effect on worm burden. Oral administration of 1/5 and 1/10 LD(50) of Larvin to S. mansoni-exposed mice induced (1) hepatomegaly and splenomegaly; (2) prominent lymphocytic aggregation in liver replacing large areas of bridging necrosis; (3) increased serum level of bilirubin and alanine aminotransferase-aspartate aminotransferase enzymes; (4) decreased serum level of albumin and total proteins; and (5) decreased RBC, hemoglobin content, leukocyte, and lymphocyte counts. No significant effect on worm burden or oviposition was noted as a result of Larvin treatment compared to controls. All doses used in mice either for infection with S. mansoni cercariae or treatment with Larvin resulted in dose dependent alterations in hepatic functions of the tested mice. These alterations were most profound in mice exposed to S. mansoni and receiving Larvin treatment. The present findings support our hypothesis and show that concurrent S. mansoni infection with exposure to Larvin adversely affect liver functions and seriously alter hematological, biochemical, and hepatic enzymes parameters in outbred albino mice. These findings warrant further investigation and reinforce the need to minimize exposure to insecticide in both natural field settings and the broader environment.
暴露于曼氏血吸虫并接受杀虫剂Larvin治疗的小鼠,加速肝损伤的风险增加。为了探究这一假设,比较了暴露于曼氏血吸虫和未暴露于该虫的远交白化小鼠接受Larvin治疗后的不良反应。通过对肝脏和脾脏进行宏观和微观检查、评估多项血液学、生化和肝酶参数以及对虫负荷的影响,来评估Larvin联合治疗对曼氏血吸虫感染进程和结果的影响。对暴露于曼氏血吸虫的小鼠口服1/5和1/10 LD(50)的Larvin,会导致:(1) 肝肿大和脾肿大;(2) 肝脏中明显的淋巴细胞聚集,取代大片桥接坏死区域;(3) 血清胆红素水平以及丙氨酸转氨酶-天冬氨酸转氨酶水平升高;(4) 血清白蛋白和总蛋白水平降低;(5) 红细胞、血红蛋白含量、白细胞和淋巴细胞计数减少。与对照组相比,Larvin治疗对虫负荷或产卵未产生显著影响。用于感染曼氏血吸虫尾蚴或治疗的Larvin的所有剂量,均导致受试小鼠肝功能出现剂量依赖性改变。这些改变在暴露于曼氏血吸虫并接受Larvin治疗的小鼠中最为显著。本研究结果支持了我们的假设,并表明曼氏血吸虫感染与暴露于Larvin同时发生,会对远交白化小鼠的肝功能产生不利影响,并严重改变血液学、生化和肝酶参数。这些发现值得进一步研究,并强化了在自然野外环境和更广泛环境中尽量减少杀虫剂暴露的必要性。