• 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

纳米结构二氧化硅经口给予大鼠的毒性评价:对免疫系统功能的影响。

Toxicity Evaluation of Nanostructured Silica Orally Administered to Rats: Influence on Immune System Function.

作者信息

Gmoshinski Ivan V, Shipelin Vladimir A, Shumakova Antonina A, Trushina Eleonora N, Mustafina Oksana K, Safenkova Irina V, Khotimchenko Sergey A, Nikityuk Dmitry B, Tutelyan Viktor A

机构信息

Federal Research Centre of Nutrition and Biotechnology, Moscow 109240, Russia.

Plekhanov Russian University of Economics, Moscow 115093, Russia.

出版信息

Nanomaterials (Basel). 2020 Oct 26;10(11):2126. doi: 10.3390/nano10112126.

DOI:10.3390/nano10112126
PMID:33114664
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7693904/
Abstract

The experimental data on the oral toxicity of nanostructured amorphous silica (SiO), widely used in food supplements, pharmaceuticals, and cosmetics, in terms of its in vivo effect on the immune system, are contradictory. Therefore, this study aimed to assess the rat's immune function after SiO oral administration. In the first experiment, SiO was daily orally administered to Wistar rats for 92 days in doses of 0.1, 1.0, 10, and 100 mg/kg of body weight (bw). In the second 28-day experiment, SiO in a dose of 100 mg/kg bw was daily orally administered to rats parenterally immunized with the food allergen ovalbumin (OVA) for the reproduction of systemic anaphylaxis reaction. Together with integral indices, we assessed intestinal permeability to protein macromolecules; hematology; CD45RA+, CD3+, CD4+, CD8+, and CD161a+ cells; cytokines TNF-α, IL-6, and IL-10; and IgG to OVA. The results obtained showed that SiO has no effect on the severity of the anaphylactic reaction, but is capable inducing a toxic effect on the T-cell immune systems of rats. Estimated no observed adverse effect level NOAEL for SiO ranges up to 100 mg/kg bw in terms of its daily consumption for 1-3 months. Using SiO as a food additive should be the subject of regulation.

摘要

广泛应用于食品补充剂、药品和化妆品中的纳米结构无定形二氧化硅(SiO),就其对免疫系统的体内影响而言,关于其口服毒性的实验数据相互矛盾。因此,本研究旨在评估口服SiO后大鼠的免疫功能。在第一个实验中,以0.1、1.0、10和100mg/kg体重(bw)的剂量,每天给Wistar大鼠口服SiO,持续92天。在第二个为期28天的实验中,以100mg/kg bw的剂量,每天给经食物过敏原卵清蛋白(OVA)进行肠外免疫的大鼠口服SiO,以重现全身过敏反应。除了整体指标外,我们还评估了肠道对蛋白质大分子的通透性、血液学、CD45RA +、CD3 +、CD4 +、CD8 +和CD161a +细胞、细胞因子TNF-α、IL-6和IL-10以及针对OVA的IgG。所得结果表明,SiO对过敏反应的严重程度没有影响,但能够对大鼠的T细胞免疫系统产生毒性作用。就SiO连续1至3个月的每日摄入量而言,估计其未观察到有害作用水平(NOAEL)高达100mg/kg bw。将SiO用作食品添加剂应受到监管。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acd2/7693904/316ef1ebabac/nanomaterials-10-02126-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acd2/7693904/1f03b217ecf4/nanomaterials-10-02126-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acd2/7693904/408d7c676db7/nanomaterials-10-02126-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acd2/7693904/9ff87ef42fdf/nanomaterials-10-02126-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acd2/7693904/e204e357b80a/nanomaterials-10-02126-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acd2/7693904/6e0a416c4a16/nanomaterials-10-02126-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acd2/7693904/d0e5faa6b8a5/nanomaterials-10-02126-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acd2/7693904/316ef1ebabac/nanomaterials-10-02126-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acd2/7693904/1f03b217ecf4/nanomaterials-10-02126-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acd2/7693904/408d7c676db7/nanomaterials-10-02126-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acd2/7693904/9ff87ef42fdf/nanomaterials-10-02126-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acd2/7693904/e204e357b80a/nanomaterials-10-02126-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acd2/7693904/6e0a416c4a16/nanomaterials-10-02126-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acd2/7693904/d0e5faa6b8a5/nanomaterials-10-02126-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acd2/7693904/316ef1ebabac/nanomaterials-10-02126-g007.jpg

相似文献

1
Toxicity Evaluation of Nanostructured Silica Orally Administered to Rats: Influence on Immune System Function.纳米结构二氧化硅经口给予大鼠的毒性评价:对免疫系统功能的影响。
Nanomaterials (Basel). 2020 Oct 26;10(11):2126. doi: 10.3390/nano10112126.
2
[Toxicological assessment of nanostructured silica. IV. Immunological and allergological indices in animals sensitized with food allergen and final discussioin].[纳米结构二氧化硅的毒理学评估。IV。用食物过敏原致敏的动物的免疫学和变应性指标及最终讨论]
Vopr Pitan. 2015;84(5):102-11.
3
[Toxicological assessment of nanostructured silica. I. Integral indices, adducts of DNA, tissue thiols and apoptosis in liver].[纳米结构二氧化硅的毒理学评估。I. 整体指标、DNA加合物、组织硫醇与肝脏中的细胞凋亡]
Vopr Pitan. 2014;83(3):52-62.
4
[Toxicological assessment of nanostructured silica. III. Microecological, hematological indices, state of cellular immunity].纳米结构二氧化硅的毒理学评估。III. 微生态、血液学指标及细胞免疫状态
Vopr Pitan. 2015;84(4):55-65.
5
[Peroral toxicological assessment of bentonite nanoclay used in the food industry].[食品工业中使用的膨润土纳米粘土的经口毒理学评估]
Vopr Pitan. 2020;89(3):71-85. doi: 10.24411/0042-8833-2020-10031. Epub 2020 May 18.
6
[Lead toxicity at its joint administration with nanostructured silica].[铅与纳米结构二氧化硅联合给药时的毒性]
Vopr Pitan. 2015;84(2):10-8.
7
Toxicity of colloidal silica nanoparticles administered orally for 90 days in rats.大鼠口服胶体二氧化硅纳米颗粒90天的毒性研究
Int J Nanomedicine. 2014 Dec 15;9 Suppl 2(Suppl 2):67-78. doi: 10.2147/IJN.S57925. eCollection 2014.
8
[Influence of dioxide titanium nanoparticles on immune system indicators in rats].[二氧化钛纳米颗粒对大鼠免疫系统指标的影响]
Vopr Pitan. 2012;81(6):47-53.
9
[Influence of nanosized amorphous silica on assimilation of vitamins B1, B2 and B6 in rats].[纳米无定形二氧化硅对大鼠维生素B1、B2和B6同化作用的影响]
Vopr Pitan. 2016;85(6):72-9.
10
Suppression of serum IgE response and systemic anaphylaxis in a food allergy model by orally administered high-dose TGF-beta.口服高剂量转化生长因子-β对食物过敏模型中血清IgE反应和全身性过敏反应的抑制作用
Int Immunol. 2005 Jun;17(6):705-12. doi: 10.1093/intimm/dxh250. Epub 2005 Apr 18.

引用本文的文献

1
Re-evaluation of silicon dioxide (E 551) as a food additive in foods for infants below 16 weeks of age and follow-up of its re-evaluation as a food additive for uses in foods for all population groups.重新评估二氧化硅(E 551)作为16周龄以下婴儿食品中的食品添加剂,并对其作为所有人群食品添加剂的重新评估进行跟踪。
EFSA J. 2024 Oct 17;22(10):e8880. doi: 10.2903/j.efsa.2024.8880. eCollection 2024 Oct.
2
Amorphous silica nanoparticles and the human gut microbiota: a relationship with multiple implications.无定形二氧化硅纳米颗粒与人类肠道微生物群:一种具有多种影响的关系。
J Nanobiotechnology. 2024 Jan 30;22(1):45. doi: 10.1186/s12951-024-02305-x.
3

本文引用的文献

1
Targeting immune cell circuits and trafficking in inflammatory bowel disease.靶向免疫细胞回路与免疫细胞迁移在炎症性肠病中的作用
Nat Immunol. 2019 Aug;20(8):970-979. doi: 10.1038/s41590-019-0415-0. Epub 2019 Jun 24.
2
The toxicity of silica nanoparticles to the immune system.硅纳米颗粒对免疫系统的毒性。
Nanomedicine (Lond). 2018 Aug 1;13(15):1939-1962. doi: 10.2217/nnm-2018-0076. Epub 2018 Aug 28.
3
Genome-wide transcriptional analysis of silica nanoparticle-induced toxicity in zebrafish embryos.二氧化硅纳米颗粒对斑马鱼胚胎毒性的全基因组转录分析。
Enterosorbents in complex therapy of food allergies: a focus on digestive disorders and systemic toxicity in children.
在食物过敏的综合治疗中使用肠吸附剂:关注儿童的消化系统紊乱和全身毒性。
Front Immunol. 2023 Oct 13;14:1210481. doi: 10.3389/fimmu.2023.1210481. eCollection 2023.
4
Toxicity and Impact of Silica Nanoparticles on the Configuration of Gut Microbiota in Immunodeficient Mice.二氧化硅纳米颗粒对免疫缺陷小鼠肠道微生物群结构的毒性及影响
Microorganisms. 2023 Apr 30;11(5):1183. doi: 10.3390/microorganisms11051183.
5
Ameliorative Effects of some Natural Antioxidants against Blood and Cardiovascular Toxicity of Oral Subchronic Exposure to Silicon Dioxide, Aluminum Oxide, or Zinc Oxide Nanoparticles in Wistar Rats.某些天然抗氧化剂对Wistar大鼠经口亚慢性暴露于二氧化硅、氧化铝或氧化锌纳米颗粒所致血液和心血管毒性的改善作用
Int J Food Sci. 2023 Mar 11;2023:8373406. doi: 10.1155/2023/8373406. eCollection 2023.
6
Frontiers in Nanotoxicology.纳米毒理学前沿
Nanomaterials (Basel). 2022 Sep 16;12(18):3219. doi: 10.3390/nano12183219.
7
Oral Toxicokinetics, Tissue Distribution, and 28-Day Oral Toxicity of Two Differently Manufactured Food Additive Silicon Dioxides.两种不同生产工艺的食品添加剂二氧化硅的经口毒代动力学、组织分布及 28 天经口毒性
Int J Mol Sci. 2022 Apr 5;23(7):4023. doi: 10.3390/ijms23074023.
Toxicol Res (Camb). 2016 Jan 20;5(2):609-620. doi: 10.1039/c5tx00383k. eCollection 2016 Mar 1.
4
Subchronic Oral Toxicity of Silica Nanoparticles and Silica Microparticles in Rats.纳米二氧化硅和微米二氧化硅经口亚慢性毒性研究。
Biomed Environ Sci. 2018 Mar;31(3):197-207. doi: 10.3967/bes2018.025.
5
Inflammation-coagulation response and thrombotic effects induced by silica nanoparticles in zebrafish embryos.二氧化硅纳米颗粒在斑马鱼胚胎中引起的炎症-凝血反应和血栓形成效应。
Nanotoxicology. 2018 Jun;12(5):470-484. doi: 10.1080/17435390.2018.1461267. Epub 2018 Apr 14.
6
Exposure to Inorganic Nanoparticles: Routes of Entry, Immune Response, Biodistribution and In Vitro/In Vivo Toxicity Evaluation.无机纳米颗粒暴露:进入途径、免疫反应、生物分布及体外/体内毒性评估
Toxics. 2017 Oct 17;5(4):29. doi: 10.3390/toxics5040029.
7
Toxicology of silica nanoparticles: an update.硅纳米粒子的毒理学:最新进展。
Arch Toxicol. 2017 Sep;91(9):2967-3010. doi: 10.1007/s00204-017-1993-y. Epub 2017 Jun 1.
8
Use of Zebrafish Larvae as a Multi-Endpoint Platform to Characterize the Toxicity Profile of Silica Nanoparticles.利用斑马鱼幼鱼作为多终点平台来描述二氧化硅纳米颗粒的毒性特征。
Sci Rep. 2016 Nov 22;6:37145. doi: 10.1038/srep37145.
9
Low-dose exposure of silica nanoparticles induces cardiac dysfunction via neutrophil-mediated inflammation and cardiac contraction in zebrafish embryos.低剂量二氧化硅纳米颗粒暴露通过中性粒细胞介导的炎症和斑马鱼胚胎心脏收缩诱导心脏功能障碍。
Nanotoxicology. 2016;10(5):575-85. doi: 10.3109/17435390.2015.1102981. Epub 2015 Nov 9.
10
Biodistribution, excretion, and toxicity of mesoporous silica nanoparticles after oral administration depend on their shape.口服介孔硅纳米颗粒后的生物分布、排泄和毒性取决于其形状。
Nanomedicine. 2015 Nov;11(8):1915-24. doi: 10.1016/j.nano.2015.07.004. Epub 2015 Jul 31.