4.7 Article

Comparison of Selenium Nanoparticles and Sodium Selenite on the Alleviation of Early Atherosclerosis by Inhibiting Endothelial Dysfunction and Inflammation in Apolipoprotein E-Deficient Mice

Journal

Publisher

MDPI
DOI: 10.3390/ijms222111612

Keywords

sodium selenite; selenium nanoparticles; atherosclerosis; inflammation; endothelial dysfunction

Funding

  1. National Natural Science Foundation of China [21771068]
  2. Shenzhen Fundamental Research Program [JCYJ20200109105836705]

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This study demonstrated that chitosan-stabilized selenium nanoparticles (CS-SeNPs) and Na2SeO3 have significant anti-atherosclerotic activity in a high-fat-diet-fed mouse model of atherosclerosis. They were found to alleviate vascular endothelial dysfunction and inflammation, leading to reduced atherosclerotic lesions in mouse aortae. Importantly, CS-SeNPs showed potential for atherosclerosis prevention with lower toxicity compared to Na2SeO3. These findings suggest that selenium supplementation may be a promising therapeutic strategy for atherosclerosis.
Atherosclerosis and related cardiovascular diseases represent the greatest threats to human health, worldwide. Previous animal studies showed that selenium nanoparticles (SeNPs) and Na2SeO3 might have anti-atherosclerotic activity, but the underlying mechanisms are poorly elucidated. This study compared the anti-atherosclerotic activity of SeNPs stabilized with chitosan (CS-SeNPs) and Na2SeO3 and the related mechanism in a high-fat-diet-fed apolipoprotein E-deficient mouse model of atherosclerosis. The results showed that oral administration of both CS-SeNPs and Na2SeO3 (40 mu g Se/kg/day) for 10 weeks significantly reduced atherosclerotic lesions in mouse aortae. Mechanistically, CS-SeNPs and Na2SeO3 not only alleviated vascular endothelial dysfunction, as evidenced by the increase of serum nitric oxide level and the decrease of aortic adhesion molecule expression, but also vascular inflammation, as evidenced by the decrease of macrophage recruitment as well as the expression of proinflammatory molecules. Importantly, these results were replicated within in-vivo experiments on the cultured human endothelial cell line EA.hy926. Overall, CS-SeNPs had a comparable effect with Na2SeO3 but might have more potential in atherosclerosis prevention due to its lower toxicity. Together, these results provide more insights into the mechanisms of selenium against atherosclerosis and further highlight the potential of selenium supplementation as a therapeutic strategy for atherosclerosis.

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