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A Bioactive Olive Pomace Extract Prevents the Death of Murine Cortical Neurons Triggered by NMDAR Over-Activation

We have recently demonstrated that bioactive molecules, extracted by high pressure and temperature from olive pomace, counteract calcium-induced cell damage to different cell lines. Here, our aim was to study the effect of the same extract on murine cortical neurons, since the preservation of the in...

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Autores principales: Franchi, Alice, Pedrazzi, Marco, Casazza, Alessandro Alberto, Millo, Enrico, Damonte, Gianluca, Salis, Annalisa, Liessi, Nara, Onofri, Franco, Marte, Antonella, Casagrande, Silvia, De Tullio, Roberta, Perego, Patrizia, Averna, Monica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7839963/
https://www.ncbi.nlm.nih.gov/pubmed/32987671
http://dx.doi.org/10.3390/molecules25194385
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author Franchi, Alice
Pedrazzi, Marco
Casazza, Alessandro Alberto
Millo, Enrico
Damonte, Gianluca
Salis, Annalisa
Liessi, Nara
Onofri, Franco
Marte, Antonella
Casagrande, Silvia
De Tullio, Roberta
Perego, Patrizia
Averna, Monica
author_facet Franchi, Alice
Pedrazzi, Marco
Casazza, Alessandro Alberto
Millo, Enrico
Damonte, Gianluca
Salis, Annalisa
Liessi, Nara
Onofri, Franco
Marte, Antonella
Casagrande, Silvia
De Tullio, Roberta
Perego, Patrizia
Averna, Monica
author_sort Franchi, Alice
collection PubMed
description We have recently demonstrated that bioactive molecules, extracted by high pressure and temperature from olive pomace, counteract calcium-induced cell damage to different cell lines. Here, our aim was to study the effect of the same extract on murine cortical neurons, since the preservation of the intracellular Ca(2+)-homeostasis is essential for neuronal function and survival. Accordingly, we treated neurons with different stimuli in order to evoke cytotoxic glutamatergic activation. In these conditions, the high-pressure and temperature extract from olive pomace (HPTOPE) only abolished the effects of N-methyl-d-aspartate (NMDA). Particularly, we observed that HPTOPE was able to promote the neuron rescue from NMDA-induced cell death. Moreover, we demonstrated that HPTOPE is endowed with the ability to maintain the intracellular Ca(2+)-homeostasis following NMDA receptor overactivation, protecting neurons from Ca(2+)-induced adverse effects, including aberrant calpain proteolytic activity. Moreover, we highlight the importance of the extraction conditions used that, without producing toxic molecules, allow us to obtain protecting molecules belonging to proanthocyanidin derivatives like procyanidin B2. In conclusion, we can hypothesize that HPTOPE, due to its functional and nontoxic properties on neuronal primary culture, can be utilized for future therapeutic interventions for neurodegeneration.
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spelling pubmed-78399632021-01-28 A Bioactive Olive Pomace Extract Prevents the Death of Murine Cortical Neurons Triggered by NMDAR Over-Activation Franchi, Alice Pedrazzi, Marco Casazza, Alessandro Alberto Millo, Enrico Damonte, Gianluca Salis, Annalisa Liessi, Nara Onofri, Franco Marte, Antonella Casagrande, Silvia De Tullio, Roberta Perego, Patrizia Averna, Monica Molecules Article We have recently demonstrated that bioactive molecules, extracted by high pressure and temperature from olive pomace, counteract calcium-induced cell damage to different cell lines. Here, our aim was to study the effect of the same extract on murine cortical neurons, since the preservation of the intracellular Ca(2+)-homeostasis is essential for neuronal function and survival. Accordingly, we treated neurons with different stimuli in order to evoke cytotoxic glutamatergic activation. In these conditions, the high-pressure and temperature extract from olive pomace (HPTOPE) only abolished the effects of N-methyl-d-aspartate (NMDA). Particularly, we observed that HPTOPE was able to promote the neuron rescue from NMDA-induced cell death. Moreover, we demonstrated that HPTOPE is endowed with the ability to maintain the intracellular Ca(2+)-homeostasis following NMDA receptor overactivation, protecting neurons from Ca(2+)-induced adverse effects, including aberrant calpain proteolytic activity. Moreover, we highlight the importance of the extraction conditions used that, without producing toxic molecules, allow us to obtain protecting molecules belonging to proanthocyanidin derivatives like procyanidin B2. In conclusion, we can hypothesize that HPTOPE, due to its functional and nontoxic properties on neuronal primary culture, can be utilized for future therapeutic interventions for neurodegeneration. MDPI 2020-09-24 /pmc/articles/PMC7839963/ /pubmed/32987671 http://dx.doi.org/10.3390/molecules25194385 Text en © 2020 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
Franchi, Alice
Pedrazzi, Marco
Casazza, Alessandro Alberto
Millo, Enrico
Damonte, Gianluca
Salis, Annalisa
Liessi, Nara
Onofri, Franco
Marte, Antonella
Casagrande, Silvia
De Tullio, Roberta
Perego, Patrizia
Averna, Monica
A Bioactive Olive Pomace Extract Prevents the Death of Murine Cortical Neurons Triggered by NMDAR Over-Activation
title A Bioactive Olive Pomace Extract Prevents the Death of Murine Cortical Neurons Triggered by NMDAR Over-Activation
title_full A Bioactive Olive Pomace Extract Prevents the Death of Murine Cortical Neurons Triggered by NMDAR Over-Activation
title_fullStr A Bioactive Olive Pomace Extract Prevents the Death of Murine Cortical Neurons Triggered by NMDAR Over-Activation
title_full_unstemmed A Bioactive Olive Pomace Extract Prevents the Death of Murine Cortical Neurons Triggered by NMDAR Over-Activation
title_short A Bioactive Olive Pomace Extract Prevents the Death of Murine Cortical Neurons Triggered by NMDAR Over-Activation
title_sort bioactive olive pomace extract prevents the death of murine cortical neurons triggered by nmdar over-activation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7839963/
https://www.ncbi.nlm.nih.gov/pubmed/32987671
http://dx.doi.org/10.3390/molecules25194385
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