Cargando…

Evaluation of the Antioxidant Activity of the Marine Pyrroloiminoquinone Makaluvamines

Makaluvamines are pyrroloiminoquinones isolated from Zyzzya sponges. Until now, they have been described as topoisomerase II inhibitors with cytotoxic effects in diverse tumor cell lines. In the present work, seven makaluvamines were tested in several antioxidant assays in primary cortical neurons a...

Descripción completa

Detalles Bibliográficos
Autores principales: Alonso, Eva, Alvariño, Rebeca, Leirós, Marta, Tabudravu, Jioji N., Feussner, Klaus, Dam, Miriam A., Rateb, Mostafa E., Jaspars, Marcel, Botana, Luis M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5128740/
https://www.ncbi.nlm.nih.gov/pubmed/27801775
http://dx.doi.org/10.3390/md14110197
_version_ 1782470462771560448
author Alonso, Eva
Alvariño, Rebeca
Leirós, Marta
Tabudravu, Jioji N.
Feussner, Klaus
Dam, Miriam A.
Rateb, Mostafa E.
Jaspars, Marcel
Botana, Luis M.
author_facet Alonso, Eva
Alvariño, Rebeca
Leirós, Marta
Tabudravu, Jioji N.
Feussner, Klaus
Dam, Miriam A.
Rateb, Mostafa E.
Jaspars, Marcel
Botana, Luis M.
author_sort Alonso, Eva
collection PubMed
description Makaluvamines are pyrroloiminoquinones isolated from Zyzzya sponges. Until now, they have been described as topoisomerase II inhibitors with cytotoxic effects in diverse tumor cell lines. In the present work, seven makaluvamines were tested in several antioxidant assays in primary cortical neurons and neuroblastoma cells. Among the alkaloids studied, makaluvamine J was the most active in all the assays. This compound was able to reduce the mitochondrial damage elicited by the well-known stressor H(2)O(2). The antioxidant properties of makaluvamine J are related to an improvement of the endogenous antioxidant defenses of glutathione and catalase. SHSY5Y assays proved that this compound acts as a Nrf2 activator leading to an improvement of antioxidant defenses. A low concentration of 10 nM is able to reduce the reactive oxygen species release and maintain a correct mitochondrial function. Based on these results, non-substituted nitrogen in the pyrrole plus the presence of a p-hydroxystyryl without a double bond seems to be the most active structure with a complete antioxidant effect in neuronal cells.
format Online
Article
Text
id pubmed-5128740
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-51287402016-12-06 Evaluation of the Antioxidant Activity of the Marine Pyrroloiminoquinone Makaluvamines Alonso, Eva Alvariño, Rebeca Leirós, Marta Tabudravu, Jioji N. Feussner, Klaus Dam, Miriam A. Rateb, Mostafa E. Jaspars, Marcel Botana, Luis M. Mar Drugs Article Makaluvamines are pyrroloiminoquinones isolated from Zyzzya sponges. Until now, they have been described as topoisomerase II inhibitors with cytotoxic effects in diverse tumor cell lines. In the present work, seven makaluvamines were tested in several antioxidant assays in primary cortical neurons and neuroblastoma cells. Among the alkaloids studied, makaluvamine J was the most active in all the assays. This compound was able to reduce the mitochondrial damage elicited by the well-known stressor H(2)O(2). The antioxidant properties of makaluvamine J are related to an improvement of the endogenous antioxidant defenses of glutathione and catalase. SHSY5Y assays proved that this compound acts as a Nrf2 activator leading to an improvement of antioxidant defenses. A low concentration of 10 nM is able to reduce the reactive oxygen species release and maintain a correct mitochondrial function. Based on these results, non-substituted nitrogen in the pyrrole plus the presence of a p-hydroxystyryl without a double bond seems to be the most active structure with a complete antioxidant effect in neuronal cells. MDPI 2016-10-27 /pmc/articles/PMC5128740/ /pubmed/27801775 http://dx.doi.org/10.3390/md14110197 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Alonso, Eva
Alvariño, Rebeca
Leirós, Marta
Tabudravu, Jioji N.
Feussner, Klaus
Dam, Miriam A.
Rateb, Mostafa E.
Jaspars, Marcel
Botana, Luis M.
Evaluation of the Antioxidant Activity of the Marine Pyrroloiminoquinone Makaluvamines
title Evaluation of the Antioxidant Activity of the Marine Pyrroloiminoquinone Makaluvamines
title_full Evaluation of the Antioxidant Activity of the Marine Pyrroloiminoquinone Makaluvamines
title_fullStr Evaluation of the Antioxidant Activity of the Marine Pyrroloiminoquinone Makaluvamines
title_full_unstemmed Evaluation of the Antioxidant Activity of the Marine Pyrroloiminoquinone Makaluvamines
title_short Evaluation of the Antioxidant Activity of the Marine Pyrroloiminoquinone Makaluvamines
title_sort evaluation of the antioxidant activity of the marine pyrroloiminoquinone makaluvamines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5128740/
https://www.ncbi.nlm.nih.gov/pubmed/27801775
http://dx.doi.org/10.3390/md14110197
work_keys_str_mv AT alonsoeva evaluationoftheantioxidantactivityofthemarinepyrroloiminoquinonemakaluvamines
AT alvarinorebeca evaluationoftheantioxidantactivityofthemarinepyrroloiminoquinonemakaluvamines
AT leirosmarta evaluationoftheantioxidantactivityofthemarinepyrroloiminoquinonemakaluvamines
AT tabudravujiojin evaluationoftheantioxidantactivityofthemarinepyrroloiminoquinonemakaluvamines
AT feussnerklaus evaluationoftheantioxidantactivityofthemarinepyrroloiminoquinonemakaluvamines
AT dammiriama evaluationoftheantioxidantactivityofthemarinepyrroloiminoquinonemakaluvamines
AT ratebmostafae evaluationoftheantioxidantactivityofthemarinepyrroloiminoquinonemakaluvamines
AT jasparsmarcel evaluationoftheantioxidantactivityofthemarinepyrroloiminoquinonemakaluvamines
AT botanaluism evaluationoftheantioxidantactivityofthemarinepyrroloiminoquinonemakaluvamines