Does Metformin Protect Diabetic Patients from Oxidative Stress and Leukocyte-Endothelium Interactions?

[EN]Since metformin can exert beneficial vascular effects, we aimed at studying its effect on reactive oxygen species (ROS) production, antioxidant enzyme expression, levels of adhesion molecules, and leukocyte-endothelium interactions in the leukocytes from type 2 diabetic (T2D) patients. The study...

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Detalhes bibliográficos
Autores: Díaz Morales, Noelia, Rovira-Llopis, Susana, Bañuls, Celia, Lopez-Domenech, Sandra, Escribano-Lopez, Irene, Veses, Silvia, Jover, Ana, Rocha, Milagros, Hernandez-Mijares, Antonio, Victor, Victor M.
Formato: artículo
Estado:Versión publicada
Fecha de publicación:2017
País:España
Recursos:Universidad de Salamanca (USAL)
Repositorio:GREDOS. Repositorio Institucional de la Universidad de Salamanca
OAI Identifier:oai:gredos.usal.es:10366/169696
Acesso em linha:http://hdl.handle.net/10366/169696
Access Level:acceso abierto
Palavra-chave:Metformina
Diabetes tipo 2
Estrés oxidativo
Disfunción mitocondrial
Leucocitos
Interacción leucocito-endotelio
Metformin
Type 2 diabetes
Oxidative stress
Mitochondrial dysfunction
Leukocytes
Leukocyte–endothelium interaction
Diabetes Mellitus, Type 2
Oxidative Stress
Mitochondria
Endothelium, Vascular
3209 Farmacología
2411 Fisiología Humana
2411.04 Fisiología Endocrina
2407 Biología Celular
diabetes mellitus tipo II
mitocondrias
estrés oxidativo
metformina
endotelio vascular
leucocitos
Descrição
Resumo:[EN]Since metformin can exert beneficial vascular effects, we aimed at studying its effect on reactive oxygen species (ROS) production, antioxidant enzyme expression, levels of adhesion molecules, and leukocyte-endothelium interactions in the leukocytes from type 2 diabetic (T2D) patients. The study was carried out in 72 T2D patients (41 of whom were treated with metformin for at least 12 months at a dose of 1700 mg per day), and in 40 sex- and age-matched control subjects. Leukocytes from T2D patients exhibited enhanced levels of mitochondrial ROS and decreased mRNA levels of glutathione peroxidase 1 (gpx1) and sirtuin 3 (sirt3) with respect to controls, whereas metformin was shown to revert these effects. No changes were observed on total ROS production and the expression levels of superoxide dismutase 1 and catalase. Furthermore, increases in leukocyte-endothelial interactions and intercellular adhesion molecule-1 and P-selectin levels were found in T2D and were also restored in metformin-treated patients. Our findings raise the question of whether metformin could modulate the appearance of atherosclerosis in T2D patients and reduce vascular events by decreasing leukocyte oxidative stress through an increase in gpx1 and sirt3 expression, and undermining adhesion molecule levels and leukocyte-endothelium interactions.