Protective effect of quercetin and thymoquinone against genotoxicity and oxidative stress induced by ZnO nanoparticles in the Wistar rat model

IF 2.3 4区 医学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Mutation research. Genetic toxicology and environmental mutagenesis Pub Date : 2023-08-01 DOI:10.1016/j.mrgentox.2023.503661
Nuzhat Parveen , Mohammad Abdulkader Akbarsha , A.B. Latif Wani , Mohd Owais Ansari , Md Fahim Ahmad , G.G.H.A. Shadab
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Abstract

Zinc oxide nanoparticles (ZnO-NPs) are increasingly used in a variety of consumer and other commercial products. Hence, man faces the risk of exposure to ZnO-NPs and the consequent adverse health effects. Mitigation/prevention of such effects using natural products has drawn the attention of scientists. Therefore, the aim of the present study has been to find the toxic effects associated with exposure to ZnO-NPs, and the protective role of the phytochemicals thymoquinone (TQ) and quercetin (QCT) in the rat model. ZnO-NPs were administered to male Wistar rats through oral route; TQ / QCT was concurrently administered through intra-peritoneal route. The response in the animal was analyzed adopting chromosomal aberration test, micronucleus test, and comet assay of bone marrow cells to assess the genotoxicity, and biochemical assays of superoxide dismutase (SOD), catalase (CAT), lipid peroxidation (LPO), total extractable protein of liver, and reduced glutathione (GSH) of liver homogenate to monitor the changes in the antioxidant defense mechanism in response to the oxidative stress. Treatment of 300 mg/kg body weight (bw) of ZnO-NPs produced adverse effects on all aspects analyzed viz., structural chromosomal aberrations, micronuclei formation, DNA damage, SOD, catalase, lipid peroxidation, GSH, and extractable total protein of liver. Co-treatment of TQ / QCT offered protection against the toxicity induced by ZnO-NPs. The most optimum doses of TQ and QCT that offered the best protection were 18 mg/kg bw and 500 mg/kg bw, respectively. The study reveals that TQ / QCT supplementation is beneficial in the context of toxic effects of ZnO-NPs.

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槲皮素和胸腺醌对ZnO纳米颗粒诱导的Wistar大鼠遗传毒性和氧化应激的保护作用
氧化锌纳米颗粒(ZnO NP)越来越多地用于各种消费品和其他商业产品。因此,人类面临暴露于氧化锌纳米颗粒的风险以及随之而来的不良健康影响。使用天然产品减轻/预防这种影响引起了科学家的注意。因此,本研究的目的是寻找与暴露于ZnO NPs相关的毒性作用,以及植物化学物质胸腺醌(TQ)和槲皮素(QCT)在大鼠模型中的保护作用。通过口服途径给雄性Wistar大鼠施用ZnO NP;TQ/QCT通过腹膜内途径同时给药。通过染色体畸变试验、微核试验和骨髓细胞彗星试验来评估遗传毒性,并通过超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、脂质过氧化(LPO)、肝脏总可提取蛋白、,和肝匀浆的还原型谷胱甘肽(GSH),以监测抗氧化防御机制对氧化应激的反应变化。处理300mg/kg体重(bw)的ZnO NP对所分析的所有方面都产生了不良影响,即染色体结构畸变、微核形成、DNA损伤、SOD、过氧化氢酶、脂质过氧化、GSH和肝脏可提取总蛋白。TQ/QCT的联合处理提供了对ZnO NPs诱导的毒性的保护。提供最佳保护的TQ和QCT的最佳剂量分别为18毫克/公斤体重和500毫克/公斤重量。研究表明,在ZnO NP的毒性作用的背景下,补充TQ/QCT是有益的。
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来源期刊
CiteScore
3.80
自引率
5.30%
发文量
84
审稿时长
105 days
期刊介绍: Mutation Research - Genetic Toxicology and Environmental Mutagenesis (MRGTEM) publishes papers advancing knowledge in the field of genetic toxicology. Papers are welcomed in the following areas: New developments in genotoxicity testing of chemical agents (e.g. improvements in methodology of assay systems and interpretation of results). Alternatives to and refinement of the use of animals in genotoxicity testing. Nano-genotoxicology, the study of genotoxicity hazards and risks related to novel man-made nanomaterials. Studies of epigenetic changes in relation to genotoxic effects. The use of structure-activity relationships in predicting genotoxic effects. The isolation and chemical characterization of novel environmental mutagens. The measurement of genotoxic effects in human populations, when accompanied by quantitative measurements of environmental or occupational exposures. The application of novel technologies for assessing the hazard and risks associated with genotoxic substances (e.g. OMICS or other high-throughput approaches to genotoxicity testing). MRGTEM is now accepting submissions for a new section of the journal: Current Topics in Genotoxicity Testing, that will be dedicated to the discussion of current issues relating to design, interpretation and strategic use of genotoxicity tests. This section is envisaged to include discussions relating to the development of new international testing guidelines, but also to wider topics in the field. The evaluation of contrasting or opposing viewpoints is welcomed as long as the presentation is in accordance with the journal''s aims, scope, and policies.
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