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首页> 外文期刊>Toxicology Reports >Nano ubiquinone: Promising candidate for treatment of renal toxicity induced by over dose of paracetamol
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Nano ubiquinone: Promising candidate for treatment of renal toxicity induced by over dose of paracetamol

机译:纳米泛醌:用于治疗对乙酰氨基酚过量引起的肾脏毒性的有希望的候选药物

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Over doses of Paracetamol (panadol; acetaminophen) can cause life-threatening renal damage. This study compared the impact of nano-ubiquinone (Nubiq) with native ubiquinone (ubiq) reducing damage induced by Paracetamol-toxicity in rats. Paracetamol treatment produced an elevation in serum urea, uric acid, creatinine, C-reactive protein, renal nitric oxide, and lipid peroxide levels, and reductions in interleukin-10, superoxide dismutase, and glutathione levels. Meanwhile, c-Jun N-terminal kinases, vascular cell adhesion protein-1, cyclooxygenase-2 protein, and kidney injury molecule-1 were highly expressed, and NFE2-related factor 2 gene expression was down-regulated. Destruction of the epithelium, necrosis, and inflammatory cell infiltration could be observed in the renal tissue. Treatment with both ubiq an nubiq significantly ameliorated all of these signs. These findings suggest that Nubiq achieved the most significant amelioration in oxidative stress and inflammatory biomarkers in paracetamol -induced nephrotoxicity.
机译:过量的扑热息痛(泛醇;对乙酰氨基酚)会导致威胁生命的肾脏损害。这项研究比较了纳米泛醌(Nubiq)与天然泛醌(ubiq)减少对乙酰氨基酚毒性所致大鼠损伤的影响。扑热息痛的治疗使血清尿素,尿酸,肌酐,C反应蛋白,肾一氧化氮和脂质过氧化物水平升高,并降低了白介素10,超氧化物歧化酶和谷胱甘肽水平。同时,c-Jun N末端激酶,血管细胞粘附蛋白1,环氧合酶2蛋白和肾损伤分子1高表达,并且NFE2相关因子2基因表达下调。在肾组织中可以观察到上皮的破坏,坏死和炎性细胞浸润。两种ubiq和nubiq的治疗均可明显改善所有这些症状。这些发现表明,Nubiq在扑热息痛引起的肾毒性中氧化应激和炎症生物标志物的改善最明显。

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