Biol Trace Elem Res. 2026 Jun 27. doi: 10.1007/s12011-026-05201-7. Online ahead of print.
ABSTRACT
Endothelial dysfunction is one of the important pathological bases of atherosclerosis, and cardiovascular diseases caused by atherosclerosis are the first major cause of human death. Our previous studies indicated that selenium nanoparticles (SeNPs) could prevent experimental atherosclerosis in animals, while their association with endothelial dysfunction remain unclear. Meanwhile, the size and surface properties of nanomaterials have a great influence on their biological functions. In this study, we prepared SeNPs with different sizes and surface charges to study their effects on H2O2-induced endothelial dysfunction in endothelial cells and the possible mechanisms. The results showed that SeNPs pretreatment significantly reduced the endothelial cell injury and dysfunction caused by H2O2. SeNPs pretreatment also significantly inhibited H2O2-induced oxidative stress, probably by enhancing cellular Se content and antioxidant selenoprotein expression in endothelial cells. Additionally, SeNPs pretreatment reversed H2O2-induced changes of Nrf2/Keap1 pathway. Moreover, SeNPs with middle size (around 40 nm) exhibited advantage in increasing cellular Se uptake and expression of antioxidant selenoproteins compared with smaller size (around 20 nm) or larger size (around 80 nm). Overall, SeNPs protect endothelial cells from H2O2-induced endothelial dysfunction by alleviating oxidative stress, and this activity may be dependent on their particle size. These results provided a deeper understanding of the anti-endothelial dysfunction activity of SeNPs and contribute to the potential use of SeNPs as a therapeutic agent against atherosclerosis in the future.
PMID:42364050 | DOI:10.1007/s12011-026-05201-7