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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
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.
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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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