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首页> 外文期刊>Advances in Toxicology >Indium Titanium Oxide Nanoparticles Induced Hepatic Damage: Hepatoprotective Role of Novel 2-Imino-4-methyl-1, 2-Dihydropyrimido [5, 4C] Quinoline-5(6H)-one
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Indium Titanium Oxide Nanoparticles Induced Hepatic Damage: Hepatoprotective Role of Novel 2-Imino-4-methyl-1, 2-Dihydropyrimido [5, 4C] Quinoline-5(6H)-one

机译:铟钛氧化物纳米颗粒引起的肝损伤:新型2-Imino-4-methyl-1,2-Dihydropyrimido [5,4C] Quinoline-5(6H)-one的保肝作用

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Protective role of 2-imino-4-methyl-1, 2-dihydropyrimido [5, 4C] quinoline-5(6H)-one (IMDHPQ) in indium titanium oxide nanoparticles (InTiO NPs) induced hepatotoxicity was analyzed. InTiO NPs were synthesized and given orally to albino rats to assess their hepatotoxicity. NPs mediated oxidative stress and liver tissue pathology were analyzed. Altered antioxidants (GSH, GPx, and catalase) and, biochemical (SGOT, SGPT, ALP, total protein, and total bilirubin) and histopathological changes were observed due to the oxidative stress caused by InTiO NPs. Varying effects of IMDHPQ on each parameter were observed in the present study. The altered parameters of InTiO NPs exposed rats might be due to the oxidative stress caused by NPs and hepatoprotective or ameliorative efficacy of quinoline compound IMDHPQ on signaling and molecular mechanism needs further study.
机译:分析了2-亚氨基-4-甲基-1,2-二氢嘧啶基[5,4C]喹啉-5(6H)-1(IMDHPQ)在铟钛氧化物纳米颗粒(InTiO NPs)诱导的肝毒性中的保护作用。合成了InTiO NP,并口服给白化病大鼠以评估其肝毒性。分析了NPs介导的氧化应激和肝组织病理学。由于InTiO NPs引起的氧化应激,观察到抗氧化剂(GSH,GPx和过氧化氢酶),生化物质(SGOT,SGPT,ALP,总蛋白和总胆红素)的改变和组织病理学变化。在本研究中观察到IMDHPQ对每个参数的变化影响。 InTiO NPs暴露大鼠参数的改变可能是由于NPs引起的氧化应激,喹啉化合物IMDHPQ对信号传导的肝保护或改善作用,分子机制尚待进一步研究。

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