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Antioxidative and vasodilatory effects of phenolic acids in wine
Authors:Ivana Mudnic  Darko Modun  Vesna Rastija  Jonatan Vukovic  Ivica Brizic  Visnja Katalinic  Bernard Kozina  Marica Medic-Saric  Mladen Boban
Affiliation:1. Department of Pharmacology, University of Split School of Medicine, Soltanska 2, 21000 Split, Croatia;2. Department of Chemistry and Biochemistry, Faculty of Agriculture, Josip Juraj Strossmayer University of Osijek, Trg Sv. Trojstva 3, 31000 Osijek, Croatia;3. Faculty of Chemistry and Technology, University of Split, Teslina 10, 21 00 Split, Croatia;4. Department of Viticulture and Enology, Faculty of Agriculture, University of Zagreb, Svetosimunska 25, 10 000 Zagreb, Croatia;5. Department of Medicinal Chemistry, Faculty of Pharmacy and Biochemistry, University of Zagreb, A. Kovacica 1, 10 000 Zagreb, Croatia
Abstract:Phenolic acids represent important fraction of wine phenolics, but their biological effects have been scarcely investigated. We examined the interrelationship between antioxidative capacity and vasodilatory activity, two potentially beneficial biological effects, of nine phenolic acids from wine. The observed antioxidative and vasodilatory effects of the tested phenolic acids were further evaluated through quantitative structure–activity relationship (QSAR) analysis, by using molecular properties, “two-dimensional” (2D) and “three-dimensional” (3D) molecular descriptors. The antioxidative capacity of phenolic acids was measured by ferric reducing antioxidant power (FRAP) and Trolox equivalent antioxidant capacity (TEAC) methods, whereas their vasodilatory activity was determined in the precontracted rat aortic rings.FRAP and TEAC values for antioxidative capacity positively correlated, but antioxidative capacity and maximal vasodilatory effect of the acids showed a negative correlation. This was best illustrated by poor vasodilatory activity of gallic acid, which is the strongest antioxidant among the tested phenolic acids. QSAR study described how antioxidative and vasodilatory effects of phenolic acids relate to the number of hydroxyl groups in the phenyl ring, degree of compactness and branching of molecules, and three-dimensional distributions of atomic polarisability of the tested molecules.
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