• 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

恢复暴露于银纳米颗粒引起的肺部炎症和肺部功能变化的 Sprague Dawley 大鼠。

Recovery from silver-nanoparticle-exposure-induced lung inflammation and lung function changes in Sprague Dawley rats.

机构信息

Korea Conformity Laboratory, Incheon, Korea.

出版信息

Nanotoxicology. 2013 Mar;7(2):169-80. doi: 10.3109/17435390.2011.648223. Epub 2012 Jan 20.

DOI:10.3109/17435390.2011.648223
PMID:22264098
Abstract

In a previous study, the lung function, as indicated by the tidal volume, minute volume, and peak inspiration flow, decreased during 90 days of exposure to silver nanoparticles and was accompanied by inflammatory lesions in the lung morphology. Therefore, this study investigated the recovery from such lung function changes in rats following the cessation of 12 weeks of nanoparticle exposure. Male and female rats were exposed to silver nanoparticles (14-15 nm diameter) at concentrations of 0.66 × 10(6) particles/cm(3) (49 μg/m(3), low dose), 1.41 × 10(6) particles/cm(3) (117 μg/m(3), middle dose), and 3.24 × 10(6) particles/cm(3) (381 μg/m(3), high dose) for 6 h/day in an inhalation chamber for 12 weeks. The rats were then allowed to recover. The lung function was measured every week during the exposure period and after the cessation of exposure, plus animals were sacrificed after the 12-week exposure period, and 4 weeks and 12 weeks after the exposure cessation. An exposure-related lung function decrease was measured in the male rats after the 12-week exposure period and 12 weeks after the exposure cessation. In contrast, the female rats did not show a consistent lung function decrease either during the exposure period or following the exposure cessation. The histopathology showed a gradual recovery from the lung inflammation in the female rats, whereas the male rats in the high-dose group exhibited persistent inflammation throughout the 12-week recovery period. Therefore, the present results suggest a potential persistence of lung function changes and inflammation induced by silver nanoparticle exposure above the no observed adverse effect level.

摘要

在之前的研究中,潮气量、分钟通气量和吸气峰流速等肺功能在暴露于银纳米粒子 90 天后下降,并伴有肺形态学的炎症损伤。因此,本研究调查了大鼠在停止暴露 12 周纳米颗粒后,从这种肺功能变化中恢复的情况。雄性和雌性大鼠在吸入室中每天暴露于银纳米粒子(直径 14-15nm)浓度为 0.66×10(6)个/立方厘米(49μg/m(3),低剂量)、1.41×10(6)个/立方厘米(117μg/m(3),中剂量)和 3.24×10(6)个/立方厘米(381μg/m(3),高剂量),每天 6 小时,共 12 周。然后允许大鼠恢复。在暴露期间和暴露停止后每周测量肺功能,以及在 12 周暴露期结束后、暴露停止后 4 周和 12 周后处死动物。在 12 周暴露期和暴露停止后 12 周,雄性大鼠的肺功能与暴露有关,出现下降。相比之下,雌性大鼠在暴露期间或暴露停止后均未出现一致的肺功能下降。组织病理学显示,雌性大鼠的肺部炎症逐渐恢复,而高剂量组的雄性大鼠在整个 12 周恢复期间持续存在炎症。因此,本研究结果表明,银纳米颗粒暴露在无观察到不良效应水平以上,可能会持续引起肺功能变化和炎症。

相似文献

1
Recovery from silver-nanoparticle-exposure-induced lung inflammation and lung function changes in Sprague Dawley rats.恢复暴露于银纳米颗粒引起的肺部炎症和肺部功能变化的 Sprague Dawley 大鼠。
Nanotoxicology. 2013 Mar;7(2):169-80. doi: 10.3109/17435390.2011.648223. Epub 2012 Jan 20.
2
Subchronic inhalation toxicity of silver nanoparticles.银纳米颗粒的亚慢性吸入毒性
Toxicol Sci. 2009 Apr;108(2):452-61. doi: 10.1093/toxsci/kfn246. Epub 2008 Nov 25.
3
Lung function changes in Sprague-Dawley rats after prolonged inhalation exposure to silver nanoparticles.长期吸入银纳米颗粒后Sprague-Dawley大鼠的肺功能变化
Inhal Toxicol. 2008 Apr;20(6):567-74. doi: 10.1080/08958370701874671.
4
Pulmonary effects of inhalation of spark-generated silver nanoparticles in Brown-Norway and Sprague-Dawley rats.吸入火花产生的银纳米颗粒对棕色挪威大鼠和斯普拉格-道利大鼠的肺部影响。
Respir Res. 2016 Jul 19;17(1):85. doi: 10.1186/s12931-016-0407-7.
5
Recovery from welding-fume-exposure-induced lung fibrosis and pulmonary function changes in sprague dawley rats.斯普拉格-道利大鼠焊接烟尘暴露所致肺纤维化及肺功能变化的恢复情况
Toxicol Sci. 2004 Dec;82(2):608-13. doi: 10.1093/toxsci/kfh289. Epub 2004 Sep 29.
6
Gene expression profiling of kidneys from Sprague-Dawley rats following 12-week inhalation exposure to silver nanoparticles.银纳米粒子吸入染毒 12 周后 Sprague-Dawley 大鼠肾脏基因表达谱分析。
Toxicol Mech Methods. 2013 Jul;23(6):437-48. doi: 10.3109/15376516.2013.780196. Epub 2013 Mar 22.
7
Acute inhalation toxicity of silver nanoparticles.银纳米颗粒的急性吸入毒性
Toxicol Ind Health. 2011 Mar;27(2):149-54. doi: 10.1177/0748233710382540. Epub 2010 Sep 24.
8
Toxicology and carcinogenesis studies of indium phosphide (CAS No. 22398-90-7) in F344/N rats and B6C3F1 mice (inhalation studies).磷化铟(CAS编号:22398-90-7)对F344/N大鼠和B6C3F1小鼠的毒理学和致癌性研究(吸入研究)
Natl Toxicol Program Tech Rep Ser. 2001 Jul(499):7-340.
9
NTP Toxicology and Carcinogenesis Studies of Talc (CAS No. 14807-96-6)(Non-Asbestiform) in F344/N Rats and B6C3F1 Mice (Inhalation Studies).滑石(CAS编号:14807-96-6)(非石棉状)在F344/N大鼠和B6C3F1小鼠中的NTP毒理学和致癌性研究(吸入研究)
Natl Toxicol Program Tech Rep Ser. 1993 Sep;421:1-287.
10
Effect of short-term stainless steel welding fume inhalation exposure on lung inflammation, injury, and defense responses in rats.短期吸入不锈钢焊接烟尘对大鼠肺部炎症、损伤及防御反应的影响。
Toxicol Appl Pharmacol. 2007 Sep 15;223(3):234-45. doi: 10.1016/j.taap.2007.06.020. Epub 2007 Jul 6.

引用本文的文献

1
Morphometric analysis and immunobiological investigation of on the infected lung with .关于感染了……的肺部的形态计量学分析和免疫生物学研究。 你提供的原文似乎不完整,“with.”后面缺少具体内容。
Open Life Sci. 2025 Aug 20;20(1):20251110. doi: 10.1515/biol-2025-1110. eCollection 2025.
2
Tailoring innovative silver nanoparticles for modern medicine: The importance of size and shape control and functional modifications.为现代医学量身定制创新型银纳米颗粒:尺寸和形状控制以及功能修饰的重要性。
Mater Today Bio. 2025 Jul 9;33:102071. doi: 10.1016/j.mtbio.2025.102071. eCollection 2025 Aug.
3
Synthesis, Cytotoxic and Genotoxic Evaluation of Drug-Loaded Silver Nanoparticles with Mebeverine and Its Analog.
载有美贝维林及其类似物的银纳米颗粒的合成、细胞毒性和遗传毒性评估
Pharmaceuticals (Basel). 2025 Mar 12;18(3):397. doi: 10.3390/ph18030397.
4
Modular air-liquid interface aerosol exposure system (MALIES) to study toxicity of nanoparticle aerosols in 3D-cultured A549 cells in vitro.用于研究纳米颗粒气溶胶在体外 3D 培养的 A549 细胞中毒性的模块化气-液界面气溶胶暴露系统(MALIES)。
Arch Toxicol. 2024 Apr;98(4):1061-1080. doi: 10.1007/s00204-023-03673-3. Epub 2024 Feb 10.
5
Aerosol Inhalation Delivery of Ag Nanoparticles in Mice: Pharmacokinetics and Antibacterial Action.小鼠中银纳米颗粒的气溶胶吸入给药:药代动力学与抗菌作用
Antibiotics (Basel). 2023 Oct 12;12(10):1534. doi: 10.3390/antibiotics12101534.
6
Comparative in vivo toxicokinetics of silver powder, nanosilver and soluble silver compounds after oral administration to rats.口服给予大鼠后银粉、纳米银和可溶性银化合物的体内毒代动力学比较。
Arch Toxicol. 2023 Jul;97(7):1859-1872. doi: 10.1007/s00204-023-03511-6. Epub 2023 May 17.
7
Biokinetics of subacutely co-inhaled same size gold and silver nanoparticles.亚急性同吸入相同大小的金和银纳米颗粒的生物动力学。
Part Fibre Toxicol. 2023 Mar 31;20(1):9. doi: 10.1186/s12989-023-00515-z.
8
Lung Models to Evaluate Silver Nanoparticles' Toxicity and Their Impact on Human Health.用于评估银纳米颗粒毒性及其对人类健康影响的肺部模型
Nanomaterials (Basel). 2022 Jul 5;12(13):2316. doi: 10.3390/nano12132316.
9
Nanomedicine formulations for respiratory infections by inhalation delivery: Covid-19 and beyond.吸入给药治疗呼吸感染的纳米医学制剂:新冠疫情及其他
Med Hypotheses. 2022 Feb;159:110753. doi: 10.1016/j.mehy.2021.110753. Epub 2022 Jan 3.
10
Silver Nanoparticles as Potential Antiviral Agents.银纳米颗粒作为潜在的抗病毒剂。
Pharmaceutics. 2021 Nov 29;13(12):2034. doi: 10.3390/pharmaceutics13122034.