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Antioxidant Activity of Ruthenium Cyclopentadienyl Complexes Bearing Succinimidato and Phthalimidato Ligands

In these studies, we investigated the antioxidant activity of three ruthenium cyclopentadienyl complexes bearing different imidato ligands: (η(5)-cyclopentadienyl)Ru(CO)(2)-N-methoxysuccinimidato (1), (η(5)-cyclopentadienyl)Ru(CO)(2)-N-ethoxysuccinimidato (2), and (η(5)-cyclopentadienyl)Ru(CO)(2)-N-...

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Detalles Bibliográficos
Autores principales: Juszczak, Michał, Kluska, Magdalena, Kosińska, Aneta, Rudolf, Bogna, Woźniak, Katarzyna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9101797/
https://www.ncbi.nlm.nih.gov/pubmed/35566156
http://dx.doi.org/10.3390/molecules27092803
Descripción
Sumario:In these studies, we investigated the antioxidant activity of three ruthenium cyclopentadienyl complexes bearing different imidato ligands: (η(5)-cyclopentadienyl)Ru(CO)(2)-N-methoxysuccinimidato (1), (η(5)-cyclopentadienyl)Ru(CO)(2)-N-ethoxysuccinimidato (2), and (η(5)-cyclopentadienyl)Ru(CO)(2)-N-phthalimidato (3). We studied the effects of ruthenium complexes 1–3 at a low concentration of 50 µM on the viability and the cell cycle of peripheral blood mononuclear cells (PBMCs) and HL-60 leukemic cells exposed to oxidative stress induced by hydrogen peroxide (H(2)O(2)). Moreover, we examined the influence of these complexes on DNA oxidative damage, the level of reactive oxygen species (ROS), and superoxide dismutase (SOD) activity. We have observed that ruthenium complexes 1–3 increase the viability of both normal and cancer cells decreased by H(2)O(2) and also alter the HL-60 cell cycle arrested by H(2)O(2) in the sub-G1 phase. In addition, we have shown that ruthenium complexes reduce the levels of ROS and oxidative DNA damage in both cell types. They also restore SOD activity reduced by H(2)O(2). Our results indicate that ruthenium complexes 1–3 bearing succinimidato and phthalimidato ligands have antioxidant activity without cytotoxic effect at low concentrations. For this reason, the ruthenium complexes studied by us should be considered interesting molecules with clinical potential that require further detailed research.