Organelle-level toxicity of nanometals relevant to titanium implants. Original research and comprehensive literature overview

IF 2.7 4区 生物学 Q1 ANATOMY & MORPHOLOGY Tissue & cell Pub Date : 2024-11-10 DOI:10.1016/j.tice.2024.102612
Murat Zaimoglu , Kutsal Devrim Secinti , Meric A. Altinoz , Melih Bozkurt , Umit Eroglu , Omer Ozpiskin , Orkhan Mammadkhanli , Eyup Bayatli , Yusuf Sukru Caglar , Ayhan Attar
{"title":"Organelle-level toxicity of nanometals relevant to titanium implants. Original research and comprehensive literature overview","authors":"Murat Zaimoglu ,&nbsp;Kutsal Devrim Secinti ,&nbsp;Meric A. Altinoz ,&nbsp;Melih Bozkurt ,&nbsp;Umit Eroglu ,&nbsp;Omer Ozpiskin ,&nbsp;Orkhan Mammadkhanli ,&nbsp;Eyup Bayatli ,&nbsp;Yusuf Sukru Caglar ,&nbsp;Ayhan Attar","doi":"10.1016/j.tice.2024.102612","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><div>This study analyzed organelle toxicities of nanometals applied as free formulations or titanium rod-coating materials in rats.</div></div><div><h3>Methods</h3><div>All materials were injected intraperitoneally, including the physiological saline applied to the control group. The first experimental group was implanted with nanosilver-coated titanium rods, and the second, third, and fourth groups received free nanosilver at rising levels. The fifth group was implanted with nanosilver, nanocopper, and nanozinc-coated titanium rods, and the sixth group received the same nanometals as free formulations. Light and electron microscopy and ICP-Mass Spectrometry were utilized to determine the neural, hepatic, and renal toxicities and tissue metal levels.</div></div><div><h3>Results</h3><div>In brains, neuropil, myelin, and cellular damages occurred, especially in groups receiving high-dose nanosilver or nanometal combinations. Histiocyte accumulation and dark mitochondria within hepatocytes were discernible in the liver. Kidneys were the organs that were most severely affected by nanometal toxicity. The nephrotoxicity was apparent with the perturbations of the membrane infoldings and mitochondrial damage in the proximal and distal convoluted epithelia. Large angular peroxisomes developed inside the mesangial cells, and Golgi bodies increased in epithelial cells. Systemic metal levels increased on the thirtieth and prominently dropped on the sixtieth day.</div></div><div><h3>Conclusion</h3><div>These results provide insights into the extent of injury and organelle targets of nanometals and will guide optimizing the nanomaterials and implants used in the surgical practice.</div></div>","PeriodicalId":23201,"journal":{"name":"Tissue & cell","volume":"91 ","pages":"Article 102612"},"PeriodicalIF":2.7000,"publicationDate":"2024-11-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tissue & cell","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0040816624003136","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ANATOMY & MORPHOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Objective

This study analyzed organelle toxicities of nanometals applied as free formulations or titanium rod-coating materials in rats.

Methods

All materials were injected intraperitoneally, including the physiological saline applied to the control group. The first experimental group was implanted with nanosilver-coated titanium rods, and the second, third, and fourth groups received free nanosilver at rising levels. The fifth group was implanted with nanosilver, nanocopper, and nanozinc-coated titanium rods, and the sixth group received the same nanometals as free formulations. Light and electron microscopy and ICP-Mass Spectrometry were utilized to determine the neural, hepatic, and renal toxicities and tissue metal levels.

Results

In brains, neuropil, myelin, and cellular damages occurred, especially in groups receiving high-dose nanosilver or nanometal combinations. Histiocyte accumulation and dark mitochondria within hepatocytes were discernible in the liver. Kidneys were the organs that were most severely affected by nanometal toxicity. The nephrotoxicity was apparent with the perturbations of the membrane infoldings and mitochondrial damage in the proximal and distal convoluted epithelia. Large angular peroxisomes developed inside the mesangial cells, and Golgi bodies increased in epithelial cells. Systemic metal levels increased on the thirtieth and prominently dropped on the sixtieth day.

Conclusion

These results provide insights into the extent of injury and organelle targets of nanometals and will guide optimizing the nanomaterials and implants used in the surgical practice.
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
与钛植入物相关的纳米金属的细胞器级毒性。原创性研究和全面的文献综述。
目的本研究分析了纳米金属作为游离制剂或钛棒涂层材料在大鼠体内的细胞毒性:方法:所有材料均经腹腔注射,包括对照组使用的生理盐水。第一实验组植入纳米银涂层钛棒,第二、第三和第四组接受水平不断上升的游离纳米银。第五组植入纳米银、纳米铜和纳米锌涂层的钛棒,第六组接受相同的纳米金属作为游离制剂。利用光学和电子显微镜以及 ICP 质谱仪测定了神经、肝脏和肾脏的毒性以及组织中的金属含量:结果:在大脑中,神经膜、髓鞘和细胞都受到了损伤,尤其是在接受高剂量纳米银或纳米金属组合的组别中。在肝脏中可以看到组织细胞堆积和肝细胞内线粒体变黑。肾脏是受纳米金属毒性影响最严重的器官。肾脏的近端和远端髓质上皮的膜折叠和线粒体损伤使肾毒性显而易见。肾间质细胞内出现大的角状过氧化物酶体,上皮细胞内的高尔基体增多。全身金属含量在第 30 天增加,在第 60 天显著下降:这些结果有助于深入了解纳米金属的损伤程度和细胞器靶标,并将指导优化外科手术中使用的纳米材料和植入物。
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
Tissue & cell
Tissue & cell 医学-解剖学与形态学
CiteScore
3.90
自引率
0.00%
发文量
234
期刊介绍: Tissue and Cell is devoted to original research on the organization of cells, subcellular and extracellular components at all levels, including the grouping and interrelations of cells in tissues and organs. The journal encourages submission of ultrastructural studies that provide novel insights into structure, function and physiology of cells and tissues, in health and disease. Bioengineering and stem cells studies focused on the description of morphological and/or histological data are also welcomed. Studies investigating the effect of compounds and/or substances on structure of cells and tissues are generally outside the scope of this journal. For consideration, studies should contain a clear rationale on the use of (a) given substance(s), have a compelling morphological and structural focus and present novel incremental findings from previous literature.
期刊最新文献
Mandibular bone defect healing using polylactic acid-nano-hydroxyapatite-gelatin scaffold loaded with hesperidin and dental pulp stem cells in rat. Inhibition of proliferation, migration and invasion of RM-1 cells by roemerine: Insights from in vitro and in vivo studies. METTL3/IGF2BP1 promotes the development of triple-negative breast cancer by mediating m6A methylation modification of PRMT7. Decellularization of human iliac artery: A vascular scaffold for peripheral repairs with human mesenchymal cells. Therapeutic potential of adult stem cells-derived mitochondria transfer combined with curcumin administration into ARPE-19 cells in age-related macular degeneration model.
×
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