• 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

[二氧化钛纳米颗粒对幼年和成年大鼠肝脏及肾脏组织抗氧化功能和元素含量的影响]

[Effects of TiO₂ nanoparticles on antioxidant function and element content of liver and kidney tissues in young and adult rats].

作者信息

Wang Yun, Chen Zhang-jian, Ba Te, Pu Ji, Cui Xiao-xing, Jia Guang

机构信息

Department of Occupational and Environmental Health Sciences, Peking University School of Public Health, Beijing 100191, China.

出版信息

Beijing Da Xue Xue Bao Yi Xue Ban. 2014 Jun 18;46(3):395-9.

PMID:24943017
Abstract

OBJECTIVE

To compare the effect of TiO₂ nanoparticles on antioxidant function and element content of liver and kidney tissues in young and adult rats.

METHODS

Forty-eight SD male rats, half in 4-week (youth) old and half in 9-week (adult) old rats, were randomly divided into 8 groups, which were exposed to TiO₂ nanoparticles [(75 ± 15) nm, anatase] through intragastric administration at 0, 10, 50 and 200 mg/kg body weight every day for 30 days. The liver and kidney tissues were collected for antioxidant function and element content analysis.

RESULTS

200 mg/kg TiO₂ nanoparticles exposure significantly increased the liver total superoxide dismutase (T-SOD) activity and the kidney reduced glutathione (GSH)/oxidized glutathione (GSSG) ratios in young rats, and significantly decreased the liver Mo, Co, Mn and P contents and the kidney Rb and Na contents in young rats. 200 mg/kg TiO₂ nanoparticles exposure significantly increased GSH/GSSG ratios and Rb contents and decreased Na contents in the liver of adult rats. No significantly difference was found in antioxidant indexes and elements content in the kidney of adult rats between three experimental groups and control group.

CONCLUSION

TiO₂ nanoparticles can enhance the antioxidant capacity and decrease the elements content in rat liver and kidney tissues. The liver is the more sensitive target organ and the young animals are more susceptible to TiO₂ nanoparticles toxicity by the oral routes.

摘要

目的

比较二氧化钛纳米颗粒对幼年和成年大鼠肝脏及肾脏组织抗氧化功能和元素含量的影响。

方法

48只雄性SD大鼠,一半为4周龄(幼年),一半为9周龄(成年),随机分为8组,每天经口给予二氧化钛纳米颗粒[(75±15)nm,锐钛矿型],剂量分别为0、10、50和200mg/kg体重,持续30天。收集肝脏和肾脏组织进行抗氧化功能和元素含量分析。

结果

200mg/kg二氧化钛纳米颗粒暴露显著提高了幼年大鼠肝脏总超氧化物歧化酶(T-SOD)活性和肾脏还原型谷胱甘肽(GSH)/氧化型谷胱甘肽(GSSG)比值,并显著降低了幼年大鼠肝脏中钼、钴、锰和磷的含量以及肾脏中铷和钠的含量。200mg/kg二氧化钛纳米颗粒暴露显著提高了成年大鼠肝脏中GSH/GSSG比值和铷含量,并降低了钠含量。成年大鼠肾脏中抗氧化指标和元素含量在三个实验组与对照组之间未发现显著差异。

结论

二氧化钛纳米颗粒可增强大鼠肝脏和肾脏组织的抗氧化能力并降低元素含量。肝脏是更敏感的靶器官,幼年动物经口途径对二氧化钛纳米颗粒毒性更敏感。

相似文献

1
[Effects of TiO₂ nanoparticles on antioxidant function and element content of liver and kidney tissues in young and adult rats].[二氧化钛纳米颗粒对幼年和成年大鼠肝脏及肾脏组织抗氧化功能和元素含量的影响]
Beijing Da Xue Xue Bao Yi Xue Ban. 2014 Jun 18;46(3):395-9.
2
Influence of different sizes of titanium dioxide nanoparticles on hepatic and renal functions in rats with correlation to oxidative stress.不同尺寸二氧化钛纳米颗粒对大鼠肝肾功能的影响及其与氧化应激的相关性
J Toxicol Environ Health A. 2009;72(11-12):740-5. doi: 10.1080/15287390902841516.
3
[Effect of subacute combined oral exposure of titanium dioxide nanoparticles and glucose on blood glucose homeostasis in young SD rats].[二氧化钛纳米颗粒与葡萄糖亚急性联合经口暴露对幼年SD大鼠血糖稳态的影响]
Wei Sheng Yan Jiu. 2020 Jul;49(4):527-533. doi: 10.19813/j.cnki.weishengyanjiu.2020.04.001.
4
[Influence of oxidative/antioxidative biomarkers and inflammatory cytokines on rats after sub-acute orally administration of titanium dioxide nanoparticles].[亚急性经口给予二氧化钛纳米颗粒后氧化/抗氧化生物标志物及炎性细胞因子对大鼠的影响]
Beijing Da Xue Xue Bao Yi Xue Ban. 2020 Oct 18;52(5):821-827. doi: 10.19723/j.issn.1671-167X.2020.05.005.
5
Effects of exposure to BDE-99 on oxidative status of liver and kidney in adult rats.BDE-99 暴露对成年大鼠肝肾氧化状态的影响。
Toxicology. 2010 Apr 30;271(1-2):51-6. doi: 10.1016/j.tox.2010.03.006. Epub 2010 Mar 17.
6
Lipid peroxidation and antioxidant status in kidney and liver of rats treated with sulfasalazine.柳氮磺胺吡啶治疗大鼠的肾脏和肝脏中的脂质过氧化及抗氧化状态
Toxicology. 2009 Feb 27;256(3):152-6. doi: 10.1016/j.tox.2008.11.010. Epub 2008 Nov 21.
7
Effects of vanadium(V) and/or chromium(III) on L-ascorbic acid and glutathione as well as iron, zinc, and copper levels in rat liver and kidney.钒(V)和/或铬(III)对大鼠肝脏和肾脏中L-抗坏血酸、谷胱甘肽以及铁、锌和铜水平的影响。
J Toxicol Environ Health A. 2007 Apr 15;70(8):696-704. doi: 10.1080/15287390601187906.
8
[Effects of titanium dioxide nanoparticles and lipopolysaccharide on antioxidant function of liver tissues in mice].[二氧化钛纳米颗粒和脂多糖对小鼠肝脏组织抗氧化功能的影响]
Beijing Da Xue Xue Bao Yi Xue Ban. 2018 Jun 18;50(3):395-400.
9
Effects of piperine on antioxidant pathways in tissues from normal and streptozotocin-induced diabetic rats.胡椒碱对正常及链脲佐菌素诱导的糖尿病大鼠组织抗氧化途径的影响。
J Biochem Mol Toxicol. 2000;14(6):329-34. doi: 10.1002/1099-0461(2000)14:6<329::AID-JBT5>3.0.CO;2-G.
10
Determination of chemopreventive role of Foeniculum vulgare and Salvia officinalis infusion on trichloroacetic acid-induced increased serum marker enzymes lipid peroxidation and antioxidative defense systems in rats.小茴香和鼠尾草浸液对三氯乙酸诱导的大鼠血清标志物酶、脂质过氧化及抗氧化防御系统变化的化学预防作用测定
Nat Prod Res. 2008 Jan 10;22(1):66-75. doi: 10.1080/14786410701590426.

引用本文的文献

1
Oral intake of titanium dioxide nanoparticles affect the course and prognosis of ulcerative colitis in mice: involvement of the ROS-TXNIP-NLRP3 inflammasome pathway.口服二氧化钛纳米颗粒影响小鼠溃疡性结肠炎的病程和预后:涉及 ROS-TXNIP-NLRP3 炎性体途径。
Part Fibre Toxicol. 2023 Jun 22;20(1):24. doi: 10.1186/s12989-023-00535-9.
2
Protective Effect of GG on TiO Nanoparticles-Induced Oxidative Stress Damage in the Liver of Young Rats.GG对纳米二氧化钛诱导的幼鼠肝脏氧化应激损伤的保护作用
Nanomaterials (Basel). 2021 Mar 21;11(3):803. doi: 10.3390/nano11030803.
3
Tissue biodistribution of intravenously administrated titanium dioxide nanoparticles revealed blood-brain barrier clearance and brain inflammation in rat.
静脉注射二氧化钛纳米颗粒的组织生物分布揭示了大鼠血脑屏障清除和脑部炎症。
Part Fibre Toxicol. 2015 Sep 4;12:27. doi: 10.1186/s12989-015-0102-8.