Antioxidant hepatic lipid metabolism can be promoted by orally administered inorganic nanoparticles.
Jie CaiJie PengJuan FengRuocheng LiPeng RenXinwei ZangZezong WuYi LuLin LuoZhenzhen HuJiaying WangXiaomeng DaiPeng ZhaoJuan WangMi YanJian-Xin LiuRenren DengDi-Ming WangPublished in: Nature communications (2023)
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.
Keyphrases
- high fat diet
- reactive oxygen species
- low dose
- oxidative stress
- adipose tissue
- healthcare
- public health
- type diabetes
- poor prognosis
- risk assessment
- mental health
- climate change
- high intensity
- gene expression
- long non coding rna
- genome wide
- binding protein
- skeletal muscle
- health information
- gram negative
- copy number
- human health