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Antioxidant hepatic lipid metabolism can be promoted by orally administered inorganic nanoparticles
Accumulation of inorganic nanoparticles in living organisms can cause an increase in cellular reactive oxygen species (ROS) in a dose-dependent manner. Low doses of nanoparticles have shown possibilities to induce moderate ROS increases and lead to adaptive responses of biological systems, but benef...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10281969/ https://www.ncbi.nlm.nih.gov/pubmed/37339977 http://dx.doi.org/10.1038/s41467-023-39423-3 |
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author | Cai, Jie Peng, Jie Feng, Juan Li, Ruocheng Ren, Peng Zang, Xinwei Wu, Zezong Lu, Yi Luo, Lin Hu, Zhenzhen Wang, Jiaying Dai, Xiaomeng Zhao, Peng Wang, Juan Yan, Mi Liu, Jianxin Deng, Renren Wang, Diming |
author_facet | Cai, Jie Peng, Jie Feng, Juan Li, Ruocheng Ren, Peng Zang, Xinwei Wu, Zezong Lu, Yi Luo, Lin Hu, Zhenzhen Wang, Jiaying Dai, Xiaomeng Zhao, Peng Wang, Juan Yan, Mi Liu, Jianxin Deng, Renren Wang, Diming |
author_sort | Cai, Jie |
collection | PubMed |
description | Accumulation of inorganic nanoparticles in living organisms can cause an increase in cellular reactive oxygen species (ROS) in a dose-dependent manner. Low doses of nanoparticles have shown possibilities to induce moderate ROS increases and lead to adaptive responses of biological systems, but beneficial effects of such responses on metabolic health remain elusive. Here, we report that repeated oral administrations of various inorganic nanoparticles, including TiO(2), Au, and NaYF(4) nanoparticles at low doses, can promote lipid degradation and alleviate steatosis in the liver of male mice. We show that low-level uptake of nanoparticles evokes an unusual antioxidant response in hepatocytes by promoting Ces2h expression and consequently enhancing ester hydrolysis. This process can be implemented to treat specific hepatic metabolic disorders, such as fatty liver in both genetic and high-fat-diet obese mice without causing observed adverse effects. Our results demonstrate that low-dose nanoparticle administration may serve as a promising treatment for metabolic regulation. |
format | Online Article Text |
id | pubmed-10281969 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102819692023-06-22 Antioxidant hepatic lipid metabolism can be promoted by orally administered inorganic nanoparticles Cai, Jie Peng, Jie Feng, Juan Li, Ruocheng Ren, Peng Zang, Xinwei Wu, Zezong Lu, Yi Luo, Lin Hu, Zhenzhen Wang, Jiaying Dai, Xiaomeng Zhao, Peng Wang, Juan Yan, Mi Liu, Jianxin Deng, Renren Wang, Diming Nat Commun Article Accumulation of inorganic nanoparticles in living organisms can cause an increase in cellular reactive oxygen species (ROS) in a dose-dependent manner. Low doses of nanoparticles have shown possibilities to induce moderate ROS increases and lead to adaptive responses of biological systems, but beneficial effects of such responses on metabolic health remain elusive. Here, we report that repeated oral administrations of various inorganic nanoparticles, including TiO(2), Au, and NaYF(4) nanoparticles at low doses, can promote lipid degradation and alleviate steatosis in the liver of male mice. We show that low-level uptake of nanoparticles evokes an unusual antioxidant response in hepatocytes by promoting Ces2h expression and consequently enhancing ester hydrolysis. This process can be implemented to treat specific hepatic metabolic disorders, such as fatty liver in both genetic and high-fat-diet obese mice without causing observed adverse effects. Our results demonstrate that low-dose nanoparticle administration may serve as a promising treatment for metabolic regulation. Nature Publishing Group UK 2023-06-20 /pmc/articles/PMC10281969/ /pubmed/37339977 http://dx.doi.org/10.1038/s41467-023-39423-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Cai, Jie Peng, Jie Feng, Juan Li, Ruocheng Ren, Peng Zang, Xinwei Wu, Zezong Lu, Yi Luo, Lin Hu, Zhenzhen Wang, Jiaying Dai, Xiaomeng Zhao, Peng Wang, Juan Yan, Mi Liu, Jianxin Deng, Renren Wang, Diming Antioxidant hepatic lipid metabolism can be promoted by orally administered inorganic nanoparticles |
title | Antioxidant hepatic lipid metabolism can be promoted by orally administered inorganic nanoparticles |
title_full | Antioxidant hepatic lipid metabolism can be promoted by orally administered inorganic nanoparticles |
title_fullStr | Antioxidant hepatic lipid metabolism can be promoted by orally administered inorganic nanoparticles |
title_full_unstemmed | Antioxidant hepatic lipid metabolism can be promoted by orally administered inorganic nanoparticles |
title_short | Antioxidant hepatic lipid metabolism can be promoted by orally administered inorganic nanoparticles |
title_sort | antioxidant hepatic lipid metabolism can be promoted by orally administered inorganic nanoparticles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10281969/ https://www.ncbi.nlm.nih.gov/pubmed/37339977 http://dx.doi.org/10.1038/s41467-023-39423-3 |
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