CEQUINOR   05415
CENTRO DE QUIMICA INORGANICA "DR. PEDRO J. AYMONINO"
Unidad Ejecutora - UE
artículos
Título:
Interactions of rutin with the oxidovanadium (IV) cation. Anticancer improvement effects of glycosylated flavonoids
Autor/es:
QUISPE, PATRICIA; REY, MARILIN; WILLIAMS, PATRICIA A. M.; NASO, LUCIANA G.; RIZZI, ALBERTO C.; GOITIA, HELEN; MARTÍNEZ, VALERIA R.; FERRER, EVELINA G.
Revista:
NEW JOURNAL OF CHEMISTRY
Editorial:
ROYAL SOC CHEMISTRY
Referencias:
Lugar: CAMBRIDGE; Año: 2019 p. 17636 - 17646
ISSN:
1144-0546
Resumen:
This work reports the biological evaluation of the new complex Na2[VO(rut)(OH)2]5H2O (rut = rutin, aglycosylated flavonoid). The complex was different in its coordination mode (catechol-like) from thosepreviously reported, [VO(rutin)(H2O)2]2(SO4)4H2O and [VO(rut)2]4H2O (acetylacetonate-like coordination).Due to the coordination mode, the complex only improved the antioxidant activity of the ligand againstsuperoxide and hydroxyl radicals. The results show that while both 100 mM rutin and V(IV)O did not exhibitcytotoxic activity on A549 cells, the complex selectively improved the anticancer effect (IC50 = 95 mM),cellular reactive oxygen species (ROS) generation and depletion of the non-enzymatic antioxidantglutathione (GSH), producing oxidized glutathione (GSSG), and it did not affect the viability of the normalembryonic lung cell line (MRC-5) (up to 100 mM). All these data, and given the reversion of the cell killingeffect of the complex upon treatment with the antioxidant agent N-acetyl-L-cysteine (NAC), suggested anoxidative stress mechanism. Rutin and VOrut can spontaneously bind bovine serum albumin (BSA) and theycan be stored and transported by the protein.