Abstract

The polyphenol quercetin is associated with numerous beneficial health effects in various pathologies such as oxidative stress, neurodegenerative disorders, inflammation, neoplastic processes, age-related diseases, and so on. However, the molecular mechanisms underlying the effects of quercetin and its implication in the pharmaceutical practice require additional clarification. In this study we analyzed the biochemical mechanisms of quercetin effect on membrane lipids of fibroblasts cultured as three-dimensional (3D) cultures, which resemble living tissues more adequately compared to cellular monolayers. Quercetin treatment of 3D fibroblasts induced alterations of the plasma membrane phospholipid and fatty acid composition as well as in the phospholipid metabolizing enzymes sphingomyelinase and phospholipase A2. The level of sphingomyelin (SM), which acts as endogenous membrane antioxidant, was elevated due to quercetin action. Incubation of 3D fibroblasts with quercetin induced augmentation in the saturated fatty acids and reduction of all polyunsaturated fatty acids in the membrane phospholipid molecules of the plasma membranes, indicating an additional increase of the resistance to oxidative damage. Quercetin treatment reduced cholesterol susceptibility to oxidation, a phenomenon which is probably related to the observed increase in the level of SM. In addition, Western blot analysis showed augmented phosphorylation of Akt and expression of Bcl-2 in quercetin-treated cell, indicating that apoptosis was suppressed by quercetin. In conclusion, the reported results contribute to a better understanding of the beneficial effects of quercetin on the structure and functions of plasma membranes of 3D cell cultures, which are a more adequate model of living tissues.

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