Graphene oxide nanosheets induced genotoxicity and pulmonary injury in mice

Nabil A. El-Yamany , Faten F. Mohamed , Taher A. Salaheldin , Amany A. Tohamy , Walaa N. Abd El-Mohsen , Adel S. Amin
{"title":"Graphene oxide nanosheets induced genotoxicity and pulmonary injury in mice","authors":"Nabil A. El-Yamany ,&nbsp;Faten F. Mohamed ,&nbsp;Taher A. Salaheldin ,&nbsp;Amany A. Tohamy ,&nbsp;Walaa N. Abd El-Mohsen ,&nbsp;Adel S. Amin","doi":"10.1016/j.etp.2017.03.002","DOIUrl":null,"url":null,"abstract":"<div><p><span>Graphene and graphene-related materials have broadly applied in biomedical purposes due to their unique properties, thus safety evaluation of them is crucial. This study was performed to explore the genotoxic and pulmonary toxic potential of different doses of graphene oxide nanosheets’ (GOs) in mice.A total of 90 male mature mice were randomly divided into six groups of fifteen mice per each, five groups were intraperitoneally injected by GO at doses of 10, 50, 100, 250 and 500</span> <!-->μg/kg b.w once weekly in addition to the control group that was injected intraperitoneally with 0.2<!--> <!-->ml saline solution. Five animals from each group were euthanized after 7, 28 and 56<!--> <span><span><span>days post treatment. Evaluation of </span>genotoxicity<span> was performed through detection of chromosomal aberrations in bone marrow while assessment of lung injury was made by determination of </span></span>DNA fragmentation<span> in lung specimens using the alkali Comet assay, pulmonary oxidative markers estimation and finally histopathological investigations. Results revealed that GOs induced variable structural chromosomal aberrations (SCA) in bone marrow and DNA damage of lung cells that were time and dose dependent and represented by increase in%DNA in comet tail, tail moment and tail length and decrease in% head DNA in nuclei of lung of GOs-treated mice </span></span><em>versus</em><span> control groups in addition, GOs induced various changes in pulmonary oxidative stress parameters that were affected by dose and duration of treatment compared with the control as well as various pulmonary histopathological alterations were detected indicating lung injury. Conclusion: GO potentiate the induction of genotoxicity and pulmonary injury in mice in time and dose dependent manner.</span></p></div>","PeriodicalId":50465,"journal":{"name":"Experimental and Toxicologic Pathology","volume":"69 6","pages":"Pages 383-392"},"PeriodicalIF":0.0000,"publicationDate":"2017-07-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.etp.2017.03.002","citationCount":"36","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Experimental and Toxicologic Pathology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0940299317301057","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 36

Abstract

Graphene and graphene-related materials have broadly applied in biomedical purposes due to their unique properties, thus safety evaluation of them is crucial. This study was performed to explore the genotoxic and pulmonary toxic potential of different doses of graphene oxide nanosheets’ (GOs) in mice.A total of 90 male mature mice were randomly divided into six groups of fifteen mice per each, five groups were intraperitoneally injected by GO at doses of 10, 50, 100, 250 and 500 μg/kg b.w once weekly in addition to the control group that was injected intraperitoneally with 0.2 ml saline solution. Five animals from each group were euthanized after 7, 28 and 56 days post treatment. Evaluation of genotoxicity was performed through detection of chromosomal aberrations in bone marrow while assessment of lung injury was made by determination of DNA fragmentation in lung specimens using the alkali Comet assay, pulmonary oxidative markers estimation and finally histopathological investigations. Results revealed that GOs induced variable structural chromosomal aberrations (SCA) in bone marrow and DNA damage of lung cells that were time and dose dependent and represented by increase in%DNA in comet tail, tail moment and tail length and decrease in% head DNA in nuclei of lung of GOs-treated mice versus control groups in addition, GOs induced various changes in pulmonary oxidative stress parameters that were affected by dose and duration of treatment compared with the control as well as various pulmonary histopathological alterations were detected indicating lung injury. Conclusion: GO potentiate the induction of genotoxicity and pulmonary injury in mice in time and dose dependent manner.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
氧化石墨烯纳米片诱导小鼠遗传毒性和肺损伤
石墨烯及其相关材料因其独特的性能在生物医学领域有着广泛的应用,因此其安全性评价至关重要。本研究旨在探讨不同剂量氧化石墨烯纳米片(GOs)对小鼠的遗传毒性和肺毒性。将90只雄性成年小鼠随机分为6组,每组15只,在对照组腹腔注射生理盐水0.2 ml的基础上,5组分别按10、50、100、250、500 μg/kg b.w的剂量注射氧化石墨烯,每周1次。各组分别于治疗后7、28、56 d处死5只。通过检测骨髓染色体畸变来评估遗传毒性,通过碱彗星法测定肺标本的DNA片段,评估肺氧化标志物,最后进行组织病理学检查来评估肺损伤。结果表明,与对照组相比,氧化石墨烯诱导小鼠骨髓可变结构染色体畸变(SCA)和肺细胞DNA损伤具有时间和剂量依赖性,表现为彗尾、尾矩和尾长%DNA增加,肺细胞核%头部DNA减少;与对照组相比,GOs诱导受剂量和持续时间影响的肺氧化应激参数发生了各种变化,并检测到肺部各种组织病理学改变,表明肺损伤。结论:氧化石墨烯对小鼠的遗传毒性和肺损伤具有时间和剂量依赖性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
2.08
自引率
0.00%
发文量
0
审稿时长
5.3 weeks
期刊介绍: Cessation. The international multidisciplinary journal is devoted to the publication of studies covering the whole range of experimental research on disease processes and toxicology including cell biological investigations. Its aim is to support progress in the interdisciplinary cooperation of researchers working in pathobiology, toxicology, and cell biology independent of the methods applied. During the past decades increasing attention has been paid to the importance of toxic influence in the pathogenesis of human and animal diseases. This is why Experimental and Toxicologic Pathology meets the urgent need for an interdisciplinary journal felt by a wide variety of experts in medicine and biology, including pathologists, toxicologists, biologists, physicians, veterinary surgeons, pharmacists, and pharmacologists working in academic, industrial or clinical institutions.
期刊最新文献
Suppression of epithelial restitution using an inhibitor against Rho-associated coiled-coil containing protein kinase aggravates colitis through reduced epithelial expression of A-kinase anchor protein 13 Protective effect of Hesperidin and Tiger nut against Acrylamide toxicity in female rats Clinical and pathological analysis of 19 cases of medullary thyroid carcinoma without an increase in calcitonin Protective effects of melatonin on long-term administration of fluoxetine in rats Argininic acid alters markers of cellular oxidative damage in vitro: Protective role of antioxidants
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1