Mechanisms of titanium dioxide nanoparticle-induced oxidative stress and modulation of plasma glucose in mice.
Hailong HuXingpei FanYao YinQian GuoDaqian YangXiangjuan WeiBoya ZhangJing LiuQiong WuYuri OhKun ChenYujie FengLiping HouLi LiHailong HuPublished in: Environmental toxicology (2019)
Titanium dioxide nanoparticles (TiO2 NPs) are reported to increase plasma glucose levels in mice at specific doses. The production and accumulation of reactive oxygen species (ROS) is potentially the most important factor underlying the biological toxicity of TiO2 NPs but the underlying mechanisms are unclear at present. Data from genome-wide analyses showed that TiO2 NPs induce endoplasmic reticulum (ER) stress and ROS generation, leading to the inference that TiO2 NP-induced ER stress contributes to enhancement of ROS in mice. Resveratrol (Res) effectively relieved TiO2 NP-induced ER stress and ROS generation by ameliorating expression of a common set of activated genes for both processes, signifying that ER stress and ROS are closely related. TiO2 NP-induced ER stress occurred earlier than ROS generation. Upon treatment with 4-phenylbutyric acid to relieve ER stress, plasma glucose levels tended toward normal and TiO2 NP increased ROS production was inhibited. These results suggest that TiO2 NP-induced ER stress promotes the generation of ROS, in turn, triggering increased plasma glucose levels in mice. In addition, Res that displays the ability to reduce ER stress presents a dietary polyphenol antioxidant that can effectively prevent the toxicological effects of TiO2 NPs on plasma glucose metabolism.
Keyphrases
- reactive oxygen species
- cell death
- quantum dots
- dna damage
- visible light
- high glucose
- genome wide
- high fat diet induced
- drug induced
- blood glucose
- endoplasmic reticulum
- dna methylation
- endothelial cells
- gene expression
- machine learning
- skeletal muscle
- single cell
- insulin resistance
- hydrogen peroxide
- deep learning
- smoking cessation
- long non coding rna
- big data
- replacement therapy