Nitroderivatives of olive oil phenols protect HepG2 cells against oxidative stress

A series of nitroderivatives has been synthetized from natural and synthetic olive oil phenols to increase the assortment of compounds with a putative effect against Parkinson disease. Before considering the potential therapeutical and nutraceutical applications of the new compounds it was critical to assess any cytotoxic effects in the liver. The precursor compounds of the nitroderivatives have shown oxidative stress protective effects, therefore we also assessed if the new compounds counteracted oxidative stress. The antioxidant activity of nitrohydroxytyrosol (NO-HTy), nitrohydroxytyrosyl-acetate (NO-HTy-A) and ethyl-nitrohydroxytyrosyl-ether (NO-HTy-E) at 5-20μM for 20. h, as well as the protective effects of the nitroderivatives after 20. h against oxidative stress induced by tert-butylhydroperoxide (t-BOOH), were assessed in HepG2 cells. Direct treatment with the three nitroderivatives decreased ROS generation compared to the control and NO-HTy at 20μM also increased glutathione peroxidase (GPx) activity (p<0.001). Pretreatment with the three nitroderivatives at 5-20μM counteracted t-BOOH cell damage by decreasing ROS generation (p < 0.001) and malondialdehyde (MDA) levels (p<0.001), increasing reduced glutathione (p<0.001) and disminishing GPx (p<0.05) activity. NO-HTy, NO-HTy-A and NO-HTy-E decreased glutathione reductase activity (p<0.05). Conclusion: the nitroderivatives do not present cytotoxic effects in the liver and in addition may protect against the oxidative stress involved in degenerative diseases. © 2012 Elsevier Ltd.

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Main Authors: Sarriá, Beatriz, Mateos, Raquel, Gallardo, Elena, Ramos, Sonia, Martín, M. Ángeles, Bravo, Laura, Goya, Luis
Other Authors: Junta de Andalucía
Format: artículo biblioteca
Language:English
Published: Elsevier 2012
Online Access:http://hdl.handle.net/10261/63052
http://dx.doi.org/10.13039/501100004837
http://dx.doi.org/10.13039/501100011011
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spelling dig-ictan-es-10261-630522022-01-26T09:09:54Z Nitroderivatives of olive oil phenols protect HepG2 cells against oxidative stress Sarriá, Beatriz Mateos, Raquel Gallardo, Elena Ramos, Sonia Martín, M. Ángeles Bravo, Laura Goya, Luis Junta de Andalucía Ministerio de Ciencia e Innovación (España) A series of nitroderivatives has been synthetized from natural and synthetic olive oil phenols to increase the assortment of compounds with a putative effect against Parkinson disease. Before considering the potential therapeutical and nutraceutical applications of the new compounds it was critical to assess any cytotoxic effects in the liver. The precursor compounds of the nitroderivatives have shown oxidative stress protective effects, therefore we also assessed if the new compounds counteracted oxidative stress. The antioxidant activity of nitrohydroxytyrosol (NO-HTy), nitrohydroxytyrosyl-acetate (NO-HTy-A) and ethyl-nitrohydroxytyrosyl-ether (NO-HTy-E) at 5-20μM for 20. h, as well as the protective effects of the nitroderivatives after 20. h against oxidative stress induced by tert-butylhydroperoxide (t-BOOH), were assessed in HepG2 cells. Direct treatment with the three nitroderivatives decreased ROS generation compared to the control and NO-HTy at 20μM also increased glutathione peroxidase (GPx) activity (p<0.001). Pretreatment with the three nitroderivatives at 5-20μM counteracted t-BOOH cell damage by decreasing ROS generation (p < 0.001) and malondialdehyde (MDA) levels (p<0.001), increasing reduced glutathione (p<0.001) and disminishing GPx (p<0.05) activity. NO-HTy, NO-HTy-A and NO-HTy-E decreased glutathione reductase activity (p<0.05). Conclusion: the nitroderivatives do not present cytotoxic effects in the liver and in addition may protect against the oxidative stress involved in degenerative diseases. © 2012 Elsevier Ltd. This work was supported by the Grant AGR-5098 from the Junta de Andalucía and by Grants AGL2010-17579 and AGL2010-18269, and the CONSOLIDER INGENIO 2010 Programme; FUN-C-FOOD CSD2007-063 from the Spanish Ministry of Science and Innovation. Peer Reviewed 2012-12-17T12:11:37Z 2012-12-17T12:11:37Z 2012 2012-12-17T12:11:37Z artículo http://purl.org/coar/resource_type/c_6501 doi: 10.1016/j.fct.2012.07.030 issn: 0278-6915 Food and Chemical Toxicology 50(10): 3752-3758 (2012) http://hdl.handle.net/10261/63052 10.1016/j.fct.2012.07.030 http://dx.doi.org/10.13039/501100004837 http://dx.doi.org/10.13039/501100011011 22842124 en https://doi.org/10.1016/j.fct.2012.07.030 none Elsevier
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libraryname Biblioteca del ICTAN España
language English
description A series of nitroderivatives has been synthetized from natural and synthetic olive oil phenols to increase the assortment of compounds with a putative effect against Parkinson disease. Before considering the potential therapeutical and nutraceutical applications of the new compounds it was critical to assess any cytotoxic effects in the liver. The precursor compounds of the nitroderivatives have shown oxidative stress protective effects, therefore we also assessed if the new compounds counteracted oxidative stress. The antioxidant activity of nitrohydroxytyrosol (NO-HTy), nitrohydroxytyrosyl-acetate (NO-HTy-A) and ethyl-nitrohydroxytyrosyl-ether (NO-HTy-E) at 5-20μM for 20. h, as well as the protective effects of the nitroderivatives after 20. h against oxidative stress induced by tert-butylhydroperoxide (t-BOOH), were assessed in HepG2 cells. Direct treatment with the three nitroderivatives decreased ROS generation compared to the control and NO-HTy at 20μM also increased glutathione peroxidase (GPx) activity (p<0.001). Pretreatment with the three nitroderivatives at 5-20μM counteracted t-BOOH cell damage by decreasing ROS generation (p < 0.001) and malondialdehyde (MDA) levels (p<0.001), increasing reduced glutathione (p<0.001) and disminishing GPx (p<0.05) activity. NO-HTy, NO-HTy-A and NO-HTy-E decreased glutathione reductase activity (p<0.05). Conclusion: the nitroderivatives do not present cytotoxic effects in the liver and in addition may protect against the oxidative stress involved in degenerative diseases. © 2012 Elsevier Ltd.
author2 Junta de Andalucía
author_facet Junta de Andalucía
Sarriá, Beatriz
Mateos, Raquel
Gallardo, Elena
Ramos, Sonia
Martín, M. Ángeles
Bravo, Laura
Goya, Luis
format artículo
author Sarriá, Beatriz
Mateos, Raquel
Gallardo, Elena
Ramos, Sonia
Martín, M. Ángeles
Bravo, Laura
Goya, Luis
spellingShingle Sarriá, Beatriz
Mateos, Raquel
Gallardo, Elena
Ramos, Sonia
Martín, M. Ángeles
Bravo, Laura
Goya, Luis
Nitroderivatives of olive oil phenols protect HepG2 cells against oxidative stress
author_sort Sarriá, Beatriz
title Nitroderivatives of olive oil phenols protect HepG2 cells against oxidative stress
title_short Nitroderivatives of olive oil phenols protect HepG2 cells against oxidative stress
title_full Nitroderivatives of olive oil phenols protect HepG2 cells against oxidative stress
title_fullStr Nitroderivatives of olive oil phenols protect HepG2 cells against oxidative stress
title_full_unstemmed Nitroderivatives of olive oil phenols protect HepG2 cells against oxidative stress
title_sort nitroderivatives of olive oil phenols protect hepg2 cells against oxidative stress
publisher Elsevier
publishDate 2012
url http://hdl.handle.net/10261/63052
http://dx.doi.org/10.13039/501100004837
http://dx.doi.org/10.13039/501100011011
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