• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

DNA single-strand breakage in rat lung, liver and kidney after single and combined treatments of nickel and cadmium.

作者信息

Saplakoğlu U, Işcan M, Işcan M

机构信息

Middle East Technical University, Department of Biology, Ankara, Turkey.

出版信息

Mutat Res. 1997 Nov 27;394(1-3):133-40.

PMID:9434852
Abstract

Single-strand breaks were observed in rat lung and kidney after acute treatment of animals with CdCl2 (4 mg/kg body weight) injected intraperitoneally and NiCl2, (44.4 mg/kg body weight) injected subcutaneously. In the rat liver, no single-strand breakage was evident with those doses in single and combined metal treatments. The most susceptible tissue in rats to cadmium or nickel chloride treatment was the lung tissue. The single-strand breaks were higher in cadmium treatment than in nickel treatment in the rat lung. Also the response to cadmium treatment was obtained earlier than nickel. Rat kidney was also responsive to cadmium treatment. However, the response, although statistically significant, was much lower than the one obtained in rat lung. The combined treatment, which was done by administrating cadmium prior to nickel administration, reduced the number of single-strand breaks significantly and reversed them to control values in rat lung and kidney. This study confirms that cadmium and nickel create single-strand breaks when administered alone in the rat lung. This effect, which was seen in the single metal treatments, was reduced in the combined treatments.

摘要

相似文献

1
DNA single-strand breakage in rat lung, liver and kidney after single and combined treatments of nickel and cadmium.
Mutat Res. 1997 Nov 27;394(1-3):133-40.
2
Comparative studies of in vivo genotoxic effects of cadmium chloride in rat brain, kidney and liver cells.氯化镉对大鼠脑、肾和肝细胞的体内遗传毒性作用的比较研究。
Cell Mol Biol (Noisy-le-grand). 1997 Mar;43(2):203-10.
3
[DNA damage in human peripheral blood lymphocyte caused by nickel and cadmium].
Zhonghua Yu Fang Yi Xue Za Zhi. 1999 Mar;33(2):75-7.
4
The relationship between nickel chloride-induced peroxidation and DNA strand breakage in rat liver.氯化镍诱导的大鼠肝脏过氧化反应与DNA链断裂之间的关系。
Toxicol Appl Pharmacol. 1992 Nov;117(1):98-103. doi: 10.1016/0041-008x(92)90222-e.
5
The effects of cadmium on the hepatic and renal levels of reduced glutathione, the activity of glutathione S-transferase and gamma glutamyl transpeptidase.镉对肝脏和肾脏中还原型谷胱甘肽水平、谷胱甘肽S-转移酶及γ-谷氨酰转肽酶活性的影响。
J Environ Pathol Toxicol Oncol. 1999;18(1):29-35.
6
Immunotoxicity of soluble and insoluble salts of cadmium instilled intratracheally.气管内注入镉的可溶盐和不溶盐的免疫毒性。
Indian J Exp Biol. 2002 Mar;40(3):262-7.
7
Distribution of nickel, zinc, and copper in rat organs after oral administration of nickel(II) chloride.口服氯化镍(II)后大鼠器官中镍、锌和铜的分布
Biol Trace Elem Res. 2002 Winter;90(1-3):215-26. doi: 10.1385/BTER:90:1-3:215.
8
Effects of combined treatment of rats with cadmium and ionizing radiation on nucleic acids in the kidneys, liver and haemopoietic organs.镉与电离辐射联合处理大鼠对肾脏、肝脏和造血器官中核酸的影响。
Folia Biol (Praha). 2001;47(3):92-100.
9
Effects of chelating agents on tissue distribution and excretion of nickel in mice.螯合剂对小鼠体内镍的组织分布和排泄的影响。
Res Commun Mol Pathol Pharmacol. 1994 Nov;86(2):245-55.
10
Nickel distribution and DNA lesions induced in rat tissues by the carcinogen nickel carbonate.致癌物碳酸镍在大鼠组织中诱导的镍分布及DNA损伤。
Cancer Res. 1982 Sep;42(9):3544-9.

引用本文的文献

1
Construction of Mode of Action for Cadmium-Induced Renal Tubular Dysfunction Based on a Toxicity Pathway-Oriented Approach.基于毒性途径导向方法构建镉诱导肾小管功能障碍的作用模式
Front Genet. 2021 Jul 23;12:696892. doi: 10.3389/fgene.2021.696892. eCollection 2021.
2
Looking for the LOAEL or NOAEL Concentration of Nickel-Oxide Nanoparticles in a Long-Term Inhalation Exposure of Rats.寻找镍氧化物纳米颗粒在大鼠长期吸入暴露中的 LOAEL 或 NOAEL 浓度。
Int J Mol Sci. 2021 Jan 3;22(1):416. doi: 10.3390/ijms22010416.
3
Update of the risk assessment of nickel in food and drinking water.
食品和饮用水中镍的风险评估更新
EFSA J. 2020 Nov 5;18(11):e06268. doi: 10.2903/j.efsa.2020.6268. eCollection 2020 Nov.
4
Nickel Carcinogenesis Mechanism: DNA Damage.镍致癌机制:DNA 损伤。
Int J Mol Sci. 2019 Sep 21;20(19):4690. doi: 10.3390/ijms20194690.
5
Modulation of the PI3K/Akt Pathway and Bcl-2 Family Proteins Involved in Chicken's Tubular Apoptosis Induced by Nickel Chloride (NiCl₂).氯化镍(NiCl₂)诱导鸡肾小管细胞凋亡过程中PI3K/Akt信号通路及Bcl-2家族蛋白的调控作用
Int J Mol Sci. 2015 Sep 23;16(9):22989-3011. doi: 10.3390/ijms160922989.
6
Temporal changes in rat liver gene expression after acute cadmium and chromium exposure.急性镉和铬暴露后大鼠肝脏基因表达的时间变化。
PLoS One. 2015 May 19;10(5):e0127327. doi: 10.1371/journal.pone.0127327. eCollection 2015.