Comparative studies on lipid peroxidation and DNA-single strand breaks induced by lindane, DDT, chlordane and endrin in rats

E. Hassoun, M. Bagchi, D. Bagchi, S.J. Stohs
{"title":"Comparative studies on lipid peroxidation and DNA-single strand breaks induced by lindane, DDT, chlordane and endrin in rats","authors":"E. Hassoun,&nbsp;M. Bagchi,&nbsp;D. Bagchi,&nbsp;S.J. Stohs","doi":"10.1016/0742-8413(93)90013-B","DOIUrl":null,"url":null,"abstract":"<div><p>1. A variety of structurally dissimilar polyhalogenated cyclic hydrocarbons produce similar toxic effects. The molecular mechanisms involved in the production of these toxic manifestations is not known.</p><p>2. We have proposed that reactive oxygen species may be involved, and have therefore examined the time-dependent effects of lindane (30<span><math><mtext>mg</mtext><mtext>kg</mtext></math></span>), DDT (40 <span><math><mtext>mg</mtext><mtext>kg</mtext></math></span>), chlordane (l 20 <span><math><mtext>mg</mtext><mtext>kg</mtext></math></span>), and endrin (4.5 <span><math><mtext>mg</mtext><mtext>kg</mtext></math></span>) on the production of hepatic mitochondrial and microsomal lipid peroxidation and DNA single strand breaks, two indices of oxidative stress.</p><p>3. All four xenobiotics resulted in significant increases in hepatic lipid peroxidation and DNA damage. Earliest (6 hr) increases in both lipid peroxidation and DNA damage were observed following lindane adminstration. Time-dependent increases in both parameters were observed following endrin administration.</p><p>4. Maximum increases in DNA single strand breaks of 2.8- and 2.5-fold were observed 12 hr after DDT and chlordane administration, respectively, while a 4.4-fold increase was observed 24 hr after endrin adminstration.</p><p>5. The results demonstrate that the four structurally dissimilar polyhalogenated hydrocarbons produce oxidative tissue damage which may contribute to the toxic manifestations of these xenobiotics, and exhibit different toxicokinetic properties.</p></div>","PeriodicalId":72650,"journal":{"name":"Comparative biochemistry and physiology. C: Comparative pharmacology","volume":"104 3","pages":"Pages 427-431"},"PeriodicalIF":0.0000,"publicationDate":"1993-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0742-8413(93)90013-B","citationCount":"53","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Comparative biochemistry and physiology. C: Comparative pharmacology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/074284139390013B","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 53

Abstract

1. A variety of structurally dissimilar polyhalogenated cyclic hydrocarbons produce similar toxic effects. The molecular mechanisms involved in the production of these toxic manifestations is not known.

2. We have proposed that reactive oxygen species may be involved, and have therefore examined the time-dependent effects of lindane (30mgkg), DDT (40 mgkg), chlordane (l 20 mgkg), and endrin (4.5 mgkg) on the production of hepatic mitochondrial and microsomal lipid peroxidation and DNA single strand breaks, two indices of oxidative stress.

3. All four xenobiotics resulted in significant increases in hepatic lipid peroxidation and DNA damage. Earliest (6 hr) increases in both lipid peroxidation and DNA damage were observed following lindane adminstration. Time-dependent increases in both parameters were observed following endrin administration.

4. Maximum increases in DNA single strand breaks of 2.8- and 2.5-fold were observed 12 hr after DDT and chlordane administration, respectively, while a 4.4-fold increase was observed 24 hr after endrin adminstration.

5. The results demonstrate that the four structurally dissimilar polyhalogenated hydrocarbons produce oxidative tissue damage which may contribute to the toxic manifestations of these xenobiotics, and exhibit different toxicokinetic properties.

林丹、滴滴涕、氯丹和内啡肽诱导大鼠脂质过氧化和dna单链断裂的比较研究
1. 多种结构不同的多卤环烃产生相似的毒性作用。产生这些毒性表现的分子机制尚不清楚。我们提出活性氧可能参与其中,因此研究了林丹(30mgkg)、滴滴涕(40mgkg)、氯丹(120mgkg)和内啡肽(4.5 mgkg)对肝脏线粒体和微粒体脂质过氧化和DNA单链断裂(氧化应激的两个指标)产生的时间依赖性影响。所有四种外源药物均导致肝脂质过氧化和DNA损伤显著增加。林丹给药后,脂质过氧化和DNA损伤最早(6小时)增加。注射endrin后,这两个参数随时间的增加而增加。DDT和氯丹给药后12小时DNA单链断裂的最大增幅分别为2.8倍和2.5倍,endrin给药后24小时DNA单链断裂的最大增幅为4.4倍。结果表明,四种结构不同的多卤代烃会产生氧化性组织损伤,这可能是导致这些外源生物毒性表现的原因之一,并表现出不同的毒性动力学特性。
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 求助全文
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信