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Modulatory Effect of Ginger Aqueous Extract on Imidacloprid Induced Hepatotoxicity in Rats

机译:生姜水提物对吡虫啉诱导的大鼠肝毒性的调节作用

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The current study was conducted for evaluation of the hepatotoxic effect of Imidacloprid (IMI) in rats and to assess the modulatory role of Zingiber officinale Roscoe, ginger aqueous extract (GAE), against such effect. Sixty mature male rats (Rattus norvegicus) were utilized and divided into six groups (10 each); group 1 was negative control received 0.1 ml of distilled water, group 2 was positive control which received 1ml of GAE, group 3 administered with 0.1 ml of IMI, group 4:administered 1ml of GAE for 2 weeks followed by administration of 0.1ml of IMI (served as protected group), group 5 administered with 0.1 ml of IMI then 1ml of GAE for 2 weeks (served as treated group) and the last group simultaneously administered with 0.1ml of IMI and 1ml of GAE (served as combination group). Oral dosing of IMI and GAE was triple weekly (day after day) and the experimental period was three months for all groups. IMI exposure caused significant increase in alanine aminotransferase (ALT), aspartate amino transferase (AST) levels, significant decrease in total proteins, albumin and globulins in serum, IMI upregulates interleukin 6 (IL6), tumor necrosis factor- α (TNF-α) and toll like receptor 2 (TLR2) genes in the liver of rats associated with intense immuno positive reactivity of TLR2 and TNF α in the liver of IMI-treated group. Histopathological examination revealed significant alterations in the liver tissue of IMI-treated group, such as disorganization of hepatic cords replaced by mononuclear cells which surrounded by lymphocytes and mild congestion of blood vessels was also seen. In conclusion, the IMI hepatotoxic effect could be modulated by the use of GAE.
机译:当前的研究是为了评估吡虫啉(IMI)对大鼠的肝毒性作用,并评估姜水提取物姜黄提取物(GAE)对这种作用的调节作用。 60只成年雄性大鼠(Rattus norvegicus)被使用并分成六组(每组十只)。第1组为阴性对照组,接受0.1 ml蒸馏水,第2组为阳性对照组,接受1ml GAE,第3组给予0.1 ml IMI,第4组:给予1ml GAE 2周,然后给予0.1ml IMI (作为保护组),第5组先施用0.1 ml IMI,然后再施用1ml GAE,持续2周(作为治疗组),最后一组同时施用0.1ml IMI和1ml GAE(作为联合组)。 IMI和GAE的口服剂量为每周三天(日复一日),所有组的实验期均为三个月。 IMI暴露导致丙氨酸氨基转移酶(ALT),天冬氨酸氨基转移酶(AST)水平显着增加,血清总蛋白,白蛋白和球蛋白显着降低,IMI上调白介素6(IL6),肿瘤坏死因子-α(TNF-α) IMI治疗组大鼠肝脏中的Toll样受体2(TLR2)基因与TLR2和TNFα的强烈免疫阳性反应有关。组织病理学检查显示,IMI治疗组的肝组织有明显改变,例如,被淋巴细胞包围的单核细胞取代了肝索,并出现了血管轻度充血。总之,可以通过使用GAE来调节IMI的肝毒性作用。

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