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Nat Commun ; 14(1): 3643, 2023 06 20.
Article in English | MEDLINE | ID: mdl-37339977

ABSTRACT

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 TiO2, Au, and NaYF4 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.


Subject(s)
Fatty Liver , Nanoparticles , Non-alcoholic Fatty Liver Disease , Male , Mice , Animals , Antioxidants/metabolism , Lipid Metabolism , Reactive Oxygen Species/metabolism , Liver/metabolism , Fatty Liver/metabolism , Hepatocytes/metabolism , Diet, High-Fat/adverse effects , Non-alcoholic Fatty Liver Disease/metabolism , Mice, Inbred C57BL
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