Author(s):
Paixão, Joana Isabel Félix ; Dinis, Teresa C. P. ; Almeida, Leonor
Date: 2012
Persistent ID: http://hdl.handle.net/10316/109913
Origin: Estudo Geral - Universidade de Coimbra
Subject(s): Animals; Anthocyanins; Aorta; Apoptosis; Caspase 3; Caspase 9; Cattle; Cell Survival; Cytoplasm; Cytoprotection; Endothelial Cells; Enzyme Activation; Free Radical Scavengers; Glucosides; Intracellular Space; Membrane Potential, Mitochondrial; Mitochondria; Oxidation-Reduction; Peroxynitrous Acid; Protective Agents; Reactive Oxygen Species; Rhodamines; Signal Transduction; bcl-2-Associated X Protein
Description
The health-promoted benefits of anthocyanins, including vascular protective effects and antiatherogenic properties, have now been recognized, but the involved molecular mechanisms have not been well elucidated. Following our previous work on cytoprotective mechanisms of some anthocyanins against apoptosis triggered by peroxynitrite in endothelial cells, here we investigated the protective role of malvidin-3-glucoside, a major dietary anthocyanin, on such deleterious process, by exploring the interference on cellular reactive species formation and on apoptotic mitochondrial pathway. Preincubation of cells with 25 μM malvidin-3-glucoside protected efficiently endothelial cells from peroxynitrite-promoted apoptotic death, an effect which may be partially mediated by its ability to decrease the formation of reactive species after cell aggression, as assessed by the dichlorodihydrofluorescein diacetate assay and by carbonyl groups formation. Moreover, malvidin-3-glucoside inhibited mitochondrial apoptotic signaling pathways induced by peroxynitrite, by counteracting mitochondrial membrane depolarization, the activation of caspase-3 and -9, and the increase in the expression of the proapoptotic Bax protein. Altogether, our data expands our knowledge about the molecular mechanisms underlying the vascular protection afforded by malvidin-3-glucoside, and anthocyanins in general, in the context of prevention of endothelial dysfunction and atherosclerosis.
