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首页> 外文期刊>Dose-response >Quercetin and Idebenone Ameliorate Oxidative Stress, Inflammation, DNA damage, and Apoptosis Induced by Titanium Dioxide Nanoparticles in Rat Liver:
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Quercetin and Idebenone Ameliorate Oxidative Stress, Inflammation, DNA damage, and Apoptosis Induced by Titanium Dioxide Nanoparticles in Rat Liver:

机译:槲皮素和艾地苯醌改善了二氧化钛纳米颗粒在大鼠肝脏中引起的氧化应激,炎症,DNA损伤和细胞凋亡:

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Titanium dioxide nanoparticles (TiO2-NPs) are extensively used in a wide range of applications; however, many reports have investigated their nanotoxicological effect at the molecular level either in vitro or in vivo systems. The defensive roles of quercetin (Qur) or idebenone (Id) against the hepatotoxicity induced by TiO2-NPs were evaluated in the current study. The results showed that the coadministration of Qur or Id to rats intoxicated with TiO2-NPs markedly ameliorated the elevation in hepatic malondialdehyde (MDA), serum alanine amino-transferase (ALT), glucose, tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), immunoglobin G (IgG), and C-reactive protein (CRP) levels compared to their levels in TiO2-NPs-treated rats. The aforementioned antioxidants also effectively modulated the changes in the levels of serum vascular endothelial growth factor (VEGF), nitric oxide (NO), hepatic DNA breakage, caspase-3, and inhibition of drug metabolizing enzymes (cytochrome P450s; CYP4502E12E1) in rat livers induced by TiO2-NPs toxicity. The histopathological examination of the liver section showed that TiO2-NPs caused severe degeneration of most hepatocytes with an increase in collagen in the portal region, while treatment with the antioxidants in question improved liver architecture. These outcomes supported the use of Qur and Id as protective agents against the hepatotoxicity induced by TiO2-NPs and other hepatotoxic drugs.
机译:二氧化钛纳米颗粒(TiO2-NPs)广泛用于广泛的应用中。然而,许多报告已经在体外或体内系统的分子水平研究了其纳米毒理学作用。在当前的研究中评估了槲皮素(Qur)或艾地苯醌(Id)对TiO2-NP诱导的肝毒性的防御作用。结果表明,向TiO2-NPs中毒的大鼠联合施用Qur或Id可以明显改善肝丙二醛(MDA),血清丙氨酸氨基转移酶(ALT),葡萄糖,肿瘤坏死因子-α(TNF-α),与TiO2-NPs处理的大鼠中的白细胞介素6(IL-6),免疫球蛋白G(IgG)和C反应蛋白(CRP)的水平相比。上述抗氧化剂还可以有效调节大鼠肝脏中血清血管内皮生长因子(VEGF),一氧化氮(NO),肝DNA断裂,caspase-3和抑制药物代谢酶(细胞色素P450s; CYP4502E12E1)的水平TiO2-NPs诱导的毒性。肝脏切片的组织病理学检查显示,TiO2-NPs导致大多数肝细胞严重变性,并在门脉区域增加胶原蛋白,而使用抗氧化剂进行治疗可改善肝脏结构。这些结果支持使用Qur和Id作为针对TiO2-NPs和其他肝毒性药物引起的肝毒性的保护剂。

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