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维生素A、C和E对雄性Wistar大鼠中氧化锌纳米颗粒(ZnO NPs)诱导的肝脏氧化应激的保护作用。

The protective effects of vitamins A, C, and E on zinc oxide nanoparticles (ZnO NPs)-induced liver oxidative stress in male Wistar rats.

作者信息

Bayat Mojtaba, Daei Sajedeh, Ziamajidi Nasrin, Abbasalipourkabir Roghayeh, Nourian Alireza

机构信息

Department of Clinical Biochemistry, School of Medicine, Hamadan University of Medical Sciences, Hamedan, Iran.

Molecular Medicine Research Center, Hamadan University of Medical Science, Hamedan, Iran.

出版信息

Drug Chem Toxicol. 2023 Mar;46(2):209-218. doi: 10.1080/01480545.2021.2016809. Epub 2021 Dec 16.

Abstract

The ever-increasing use of zinc oxide nanoparticles (ZnO NPs) in industrial and consumer products leads to concerns about their safety. Liver is one of the most important target organs of nanoparticles after entering the body. As such, the aim of this study was to evaluate the protective effects of vitamins (Vit) A, C, and E on ZnO NPs-induced liver oxidative stress. For this task, 54 male Wistar rats were randomly divided into nine groups of six: control 1 (water), control 2 (olive oil), Vit A (1000 IU/kg), Vit C (200 mg/kg), Vit E (100 IU/kg), ZnO (200 mg/kg), ZnO + VitA, ZnO + VitC, and ZnO + VitE. The animals received ZnO for 2 weeks while treatment with Vit started one week before the ZnO administration. In order to specify oxidative stress status, total antioxidant capacity (TAC), total oxidative status and malondialdehyde were determined by colorimetric assay. In addition, the activity and gene expression of antioxidant enzymes including superoxide dismutase (SOD), glutathione peroxidase (GPx), and catalase (CAT) were evaluated by colorimetric assay kit and qRT-PCR, respectively. Moreover, histological analysis was conducted to estimate the extent of liver damage. Our results indicate that the oxidative parameters are increased while the content of TAC, antioxidant enzymes activity, and gene expression of SOD, GPX, and CAT show a significant reduction in the liver of ZnO-treated rats compared to the control (< 0.05). In contrast, the administration of Vit could significantly modulate the aforementioned changes. Overall, Vit A, E, and C can mitigate oxidative stress caused by ZnO NPs.

摘要

氧化锌纳米颗粒(ZnO NPs)在工业和消费品中的使用日益增加,这引发了人们对其安全性的担忧。肝脏是纳米颗粒进入人体后最重要的靶器官之一。因此,本研究的目的是评估维生素(Vit)A、C和E对ZnO NPs诱导的肝脏氧化应激的保护作用。为此,将54只雄性Wistar大鼠随机分为9组,每组6只:对照组1(水)、对照组2(橄榄油)、Vit A(1000 IU/kg)、Vit C(200 mg/kg)、Vit E(100 IU/kg)、ZnO(200 mg/kg)、ZnO + VitA、ZnO + VitC和ZnO + VitE。动物接受ZnO处理2周,而Vit治疗在ZnO给药前1周开始。为了确定氧化应激状态,通过比色法测定总抗氧化能力(TAC)、总氧化状态和丙二醛。此外,分别通过比色法试剂盒和qRT-PCR评估抗氧化酶超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GPx)和过氧化氢酶(CAT)的活性和基因表达。此外,进行组织学分析以评估肝脏损伤程度。我们的结果表明,与对照组相比,ZnO处理的大鼠肝脏中氧化参数增加,而TAC含量、抗氧化酶活性以及SOD、GPX和CAT的基因表达显著降低(<0.05)。相反,Vit的给药可以显著调节上述变化。总体而言,Vit A、E和C可以减轻ZnO NPs引起的氧化应激。

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