Gold Nanoparticles Supported on Ceria Nanoparticles Modulate Leukocyte–Endothelium Cell Interactions and Inflammation in Type 2 Diabetes

• Published in: Antioxidants 2022-11, Vol.11 (11), p.2297
• Main Authors: Díaz-Pozo, Pedro, Canet, Francisco, Grirrane, Abdessamad, Lopez-Domenech, Sandra, Herance, José Raul, Apostolova, Nadezda, Luna-Marco, Clara, Rovira-Llopis, Susana, Marti, Miguel, Morillas, Carlos, Rocha, Milagros, Garcia, Hermenegildo, Victor, Victor M.
• Format: Article
• Language: English
• Subjects: Antioxidants; Apoptosis; Arteriosclerosis; atherosclerosis; Body mass index; Carbohydrate metabolism; Cardiovascular diseases; Cell interactions; Cell proliferation; Cholesterol; Diabetes; Diabetes mellitus (non-insulin dependent); Diabetic neuropathy; Endothelium; Enzymes; Glucose; Gold; gold-ceria nanoparticle; Homeostasis; Hospitals; Hyperglycemia; Inflammation; Insulin resistance; Leukocyte rolling; Lipid metabolism; Nanoparticles; NF-κB protein; Oxidative stress; Physiological aspects; ROS; Toxicity; Type 2 diabetes
• ISSN: 2076-3921; 2076-3921
• DOI: 10.3390/antiox11112297

Gold-ceria nanoparticles (Au/CeO2) are known to have antioxidant properties. However, whether these nanoparticles can provide benefits in type 2 diabetes mellitus (T2D) remains unknown. This work aimed to study the effects of Au/CeO2 nanoparticles at different rates of gold purity (10, 4.4, 1.79 and 0.82) on leukocyte–endothelium interactions and inflammation in T2D patients. Anthropometric and metabolic parameters, leukocyte–endothelium interactions, ROS production and NF-κB expression were assessed in 57 T2D patients and 51 healthy subjects. T2D patients displayed higher Body Mass Index (BMI) and characteristic alterations in carbohydrate and lipid metabolism. ROS production was increased in leukocytes of T2D patients and decreased by Au/CeO2 at 0.82% gold. Interestingly, Au/CeO2 0.82% modulated leukocyte–endothelium interactions (the first step in the atherosclerotic process) by increasing leukocyte rolling velocity and decreasing rolling flux and adhesion in T2D. A static adhesion assay also revealed diminished leukocyte–endothelium interactions by Au/CeO2 0.82% treatment. NF-κB (p65) levels increased in T2D patients and were reduced by Au/CeO2 treatment. Cell proliferation, viability, and apoptosis assays demonstrated no toxicity produced by Au/CeO2 nanoparticles. These results demonstrate that Au/CeO2 nanoparticles at 0.82% exert antioxidant and anti-inflammatory actions in the leukocyte–endothelium interaction of T2D patients, suggesting a protective role against the appearance of atherosclerosis and cardiovascular diseases when this condition exists.