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Hydroxytyrosol Decreases LPS- and α-Synuclein-Induced Microglial Activation In Vitro
Neuroinflammation is a common feature shared by neurodegenerative disorders, such as Parkinson’s disease (PD), and seems to play a key role in their development and progression. Microglia cells, the principal orchestrators of neuroinflammation, can be polarized in different phenotypes, which means t...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7022576/ https://www.ncbi.nlm.nih.gov/pubmed/31906130 http://dx.doi.org/10.3390/antiox9010036 |
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author | Gallardo-Fernández, Marta Hornedo-Ortega, Ruth Alonso-Bellido, Isabel M. Rodríguez-Gómez, José A. Troncoso, Ana M. García-Parrilla, M. Carmen Venero, José L. Espinosa-Oliva, Ana M. de Pablos, Rocío M. |
author_facet | Gallardo-Fernández, Marta Hornedo-Ortega, Ruth Alonso-Bellido, Isabel M. Rodríguez-Gómez, José A. Troncoso, Ana M. García-Parrilla, M. Carmen Venero, José L. Espinosa-Oliva, Ana M. de Pablos, Rocío M. |
author_sort | Gallardo-Fernández, Marta |
collection | PubMed |
description | Neuroinflammation is a common feature shared by neurodegenerative disorders, such as Parkinson’s disease (PD), and seems to play a key role in their development and progression. Microglia cells, the principal orchestrators of neuroinflammation, can be polarized in different phenotypes, which means they are able to have anti-inflammatory, pro-inflammatory, or neurodegenerative effects. Increasing evidence supports that the traditional Mediterranean dietary pattern is related to the reduction of cognitive decline in neurodegenerative diseases. A considerable intake of plant foods, fish, and extra virgin olive oil (EVOO), as well as a moderate consumption of red wine, all characteristic of the Mediterranean diet (MD), are behind these effects. These foods are especially rich in polyphenols, being the most relevant in the MD hydroxytyrosol (HT) and their derivatives present in EVOO, which have demonstrated a wide array of biological activities. Here, we demonstrate that HT is able to reduce the inflammation induced by two different stimuli: lipopolysaccharide and α-synuclein. We also study the possible molecular mechanisms involved in the anti-inflammatory effect of HT, including the study of nuclear factor kappa B (NF-κB), mitogen-activated protein kinases (MAPKs), nicotinamide adenine dinucleotide phosphate (NADPH) oxidase, and inflammasome. Our data support the use of HT to prevent the inflammation associated with PD and shed light into the relationship between MD and this neurological disorder. |
format | Online Article Text |
id | pubmed-7022576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70225762020-03-09 Hydroxytyrosol Decreases LPS- and α-Synuclein-Induced Microglial Activation In Vitro Gallardo-Fernández, Marta Hornedo-Ortega, Ruth Alonso-Bellido, Isabel M. Rodríguez-Gómez, José A. Troncoso, Ana M. García-Parrilla, M. Carmen Venero, José L. Espinosa-Oliva, Ana M. de Pablos, Rocío M. Antioxidants (Basel) Article Neuroinflammation is a common feature shared by neurodegenerative disorders, such as Parkinson’s disease (PD), and seems to play a key role in their development and progression. Microglia cells, the principal orchestrators of neuroinflammation, can be polarized in different phenotypes, which means they are able to have anti-inflammatory, pro-inflammatory, or neurodegenerative effects. Increasing evidence supports that the traditional Mediterranean dietary pattern is related to the reduction of cognitive decline in neurodegenerative diseases. A considerable intake of plant foods, fish, and extra virgin olive oil (EVOO), as well as a moderate consumption of red wine, all characteristic of the Mediterranean diet (MD), are behind these effects. These foods are especially rich in polyphenols, being the most relevant in the MD hydroxytyrosol (HT) and their derivatives present in EVOO, which have demonstrated a wide array of biological activities. Here, we demonstrate that HT is able to reduce the inflammation induced by two different stimuli: lipopolysaccharide and α-synuclein. We also study the possible molecular mechanisms involved in the anti-inflammatory effect of HT, including the study of nuclear factor kappa B (NF-κB), mitogen-activated protein kinases (MAPKs), nicotinamide adenine dinucleotide phosphate (NADPH) oxidase, and inflammasome. Our data support the use of HT to prevent the inflammation associated with PD and shed light into the relationship between MD and this neurological disorder. MDPI 2019-12-31 /pmc/articles/PMC7022576/ /pubmed/31906130 http://dx.doi.org/10.3390/antiox9010036 Text en © 2019 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 Gallardo-Fernández, Marta Hornedo-Ortega, Ruth Alonso-Bellido, Isabel M. Rodríguez-Gómez, José A. Troncoso, Ana M. García-Parrilla, M. Carmen Venero, José L. Espinosa-Oliva, Ana M. de Pablos, Rocío M. Hydroxytyrosol Decreases LPS- and α-Synuclein-Induced Microglial Activation In Vitro |
title | Hydroxytyrosol Decreases LPS- and α-Synuclein-Induced Microglial Activation In Vitro |
title_full | Hydroxytyrosol Decreases LPS- and α-Synuclein-Induced Microglial Activation In Vitro |
title_fullStr | Hydroxytyrosol Decreases LPS- and α-Synuclein-Induced Microglial Activation In Vitro |
title_full_unstemmed | Hydroxytyrosol Decreases LPS- and α-Synuclein-Induced Microglial Activation In Vitro |
title_short | Hydroxytyrosol Decreases LPS- and α-Synuclein-Induced Microglial Activation In Vitro |
title_sort | hydroxytyrosol decreases lps- and α-synuclein-induced microglial activation in vitro |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7022576/ https://www.ncbi.nlm.nih.gov/pubmed/31906130 http://dx.doi.org/10.3390/antiox9010036 |
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