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首页> 外文期刊>International journal of toxicology >Comparative Assessment on Mechanism Underlying Renal Toxicity of Commercial Formulation of Roundup Herbicide and Glyphosate Alone in Male Albino Rat
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Comparative Assessment on Mechanism Underlying Renal Toxicity of Commercial Formulation of Roundup Herbicide and Glyphosate Alone in Male Albino Rat

机译:对循环除草剂和草甘膦商业制剂肾毒性肾毒性的机制的比较评估

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摘要

There have been major concerns that the nephrotoxicity of commercial formulations of Roundup herbicide is due to the active ingredient glyphosate. We therefore investigated and compared the mechanisms underlining the nephrotoxicity of Roundup herbicide and glyphosate alone in rat. Fifty-six adult male rats randomized into 7 groups of 8 rats per group were exposed to Roundup formulation and glyphosate alone daily by gavage at 3.6, 50.4, and 248.4 mg/kg body weight (bw) of glyphosate concentrations for 12 weeks with distilled water administered to the control group. Kidney biomarker (serum urea and creatinine, plasma cystatin-C, and neutrophil gelatinase-associated lipocalin), oxidative stress indices in the kidney tissue, activities of kidney membrane-bound enzymes (Mg-adenosine triphosphatase [ATPase], Ca-ATPase, Na/K-ATPase, and total ATPase), and histopathological changes in the kidney were monitored. Glyphosate concentration in the kidney was quantified by high-performance liquid chromatography with ultraviolet detection. Significant (P 0.05) alterations in the levels of the kidney biomarker, oxidative stress markers, and membrane-bound enzymes were observed in the rats exposed to Roundup compared to the rats exposed to glyphosate alone. Rats exposed to Roundup accumulated more glyphosate residue in their kidney tissue. Severe histopathological lesions were only seen in the kidneys of rats exposed to Roundup. The nephrotoxicity observed cannot be due to the active ingredient in the Roundup formulation, as glyphosate alone has virtually no effect on the renal function of the exposed animals. Therefore, the general claim attributing nephrotoxicity of a glyphosate-based herbicide to its active ingredient should be discouraged.
机译:主要担心圆形除草剂的商业配方的肾毒性是由于活性成分草甘膦。因此,我们研究并比较了在大鼠中单独循环除草剂和草甘膦的肾毒性下调的机制。将5六个成年雄性大鼠随机将每组8种大鼠每组暴露于每天在3.6,50.4和248.4mg / kg体重(BW)的蒸馏水中每天暴露于3.6,50.4和248.4mg / kg体重(BW),蒸馏水12周给予对照组。肾脏生物标志物(血清尿素和肌酐,血浆胱抑素-c,中性粒细胞明胶酶相关脂素),肾脏组织中的氧化应激指数,肾膜结合酶的活性(Mg-腺苷三磷酸酶[Atpase],Ca-Atpase,Na / K-ATP酶和总ATP酶),并监测肾脏的组织病理学变化。通过具有紫外检测的高效液相色谱法量化肾的草甘膦浓度。与单独暴露于草甘膦暴露于草甘膦的大鼠,在暴露于圆形的大鼠中观察到肾脏生物标志物,氧化应激标记物和膜结合酶水平的显着(P <0.05)的改变。暴露于圆形的大鼠在其肾组织中积累了更多的草甘膦残留物。仅在暴露于圆润的大鼠的肾脏中看到严重的组织病理病变。观察到的肾毒性不能是由于圆形制剂中的活性成分,因为单独的草甘膦几乎没有对暴露动物的肾功能影响。因此,应令人难发院将归因于草甘膦除草剂的肾毒性归因于其活性成分的一般索赔。

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