首页> 外文期刊>Indian Journal of Animal Research >Evaluation of acute toxicity and effects of sub-acute concentrations of copper oxide nanoparticles (CuO-NPs) on hematology, selected enzymes and histopathology of liver and kidney in Mus musculus
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Evaluation of acute toxicity and effects of sub-acute concentrations of copper oxide nanoparticles (CuO-NPs) on hematology, selected enzymes and histopathology of liver and kidney in Mus musculus

机译:评价氧化铜纳米粒子(CUO-NPS)对血液学,肝肾血液学,选定酶及肝肾组织病理学的急性毒性及影响

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Industrial use of nanoparticles and their accumulation during the recent decade have created an urgent need to assess their environmental implications. The current study deals with the evaluation of acute toxicity of copper oxide nanoparticles (CuO-NPs) in the albino mice (Mus musculus). Lethal dose of these nanoparticles in albino mice injected via intravenous route were found to be 550 mg/kg body weight (BW). Exposure of the albino mice to sub-lethal concentrations of these nanoparticles resulted in altered hematological parameters such as a significant increase in white blood cells (WBCs), a significant decrease in red blood cells (RBCs), hemoglobin (Hb) and platelets count. NPs significantly elevated the levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), urea and creatinine. Histopathological examination of liver and kidney showed that sub-lethal doses of CuO-NPs, in liver, led to rupture of hepatocytes, dilation of sinusoid space, hemorrhaging in hepatic tissues, and congestion of the central vein with red blood cells leading towards ultimate rupture. On the other hand, the kidney showed ruptured renal capsule, loss of urinary space, swelling in glomerulus, degeneration in podocysts, and cytoplasmic vacuolization.
机译:纳米粒子的工业用途及其积累始终创造了迫切需要评估其环境影响。目前的研究涉及评估白化小鼠(Mus Musculus)中氧化铜氧化物纳米颗粒(CuO-NPS)的急性毒性。通过静脉内途径注射的白化小鼠中这些纳米颗粒的致死剂量为550mg / kg体重(BW)。将白化小鼠暴露于这些纳米颗粒的亚致死浓度导致改变的血液学参数,例如白细胞(WBC)的显着增加,红细胞(RBC),血红蛋白(HB)和血小板计数显着降低。 NPS显着升高了丙氨酸氨基转移酶(ALT),天冬氨酸氨基转移酶(AST),尿素和肌酐水平。肝肾组织病理学检查表明,肝脏患者的CuO-NPS,肝脏,导致肝细胞破裂,正弦空间扩张,肝脏组织中的出血,以及中央静脉的充血,红细胞导致最终破裂。另一方面,肾脏显示出肾囊破裂,尿空间丧失,肾小球肿胀,诱导肾细胞变性,细胞质真空。

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