Low Phytanic Acid-Concentrated DHA Prevents Cognitive Deficit and Regulates Alzheimer Disease Mediators in an ApoE−/− Mice Experimental Model

[EN] Alzheimer’s disease (AD) is the main cause of dementia and cognitive impairment. It has been associated with a significant diminution of omega-3 polyunsaturated fatty acid docosahexaenoic acid (DHA) levels in the brain. Clinical trials with DHA as a treatment in neurological diseases have shown...

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Autores: Ruiz-Roso Guerra, María Belén, Echeverry Alzate, Víctor, Ruiz-Roso Calvo de Mora, Baltasar, Quintela Fernández, José Carlos, Ballesteros Rodrigálvarez, Sandra María, Lahera Juliá, Vicente, Heras Jiménez, Natalia de las, López Moreno, José Antonio, Martín Fernández, Beatriz
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2019
País:España
Institución:Universidad de León
Repositorio:BULERIA. Repositorio Institucional de la Universidad de León
OAI Identifier:oai:buleria.unileon.es:10612/24381
Acceso en línea:https://www.mdpi.com/2072-6643/11/1/11
https://hdl.handle.net/10612/24381
Access Level:acceso abierto
Palabra clave:Bioquímica
Medicina. Salud
Alzheimer’s
DHA
ApoE -/-
Phytanic acid
Inflammation
Neuroprotection
Oxidation
3207.11 Neuropatología
2302.11 Acidos Grasos
2403 Bioquímica
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spelling Low Phytanic Acid-Concentrated DHA Prevents Cognitive Deficit and Regulates Alzheimer Disease Mediators in an ApoE−/− Mice Experimental ModelRuiz-Roso Guerra, María BelénEcheverry Alzate, VíctorRuiz-Roso Calvo de Mora, BaltasarQuintela Fernández, José CarlosBallesteros Rodrigálvarez, Sandra MaríaLahera Juliá, VicenteHeras Jiménez, Natalia de lasLópez Moreno, José AntonioMartín Fernández, BeatrizBioquímicaMedicina. SaludAlzheimer’sDHAApoE -/-Phytanic acidInflammationNeuroprotectionOxidation3207.11 Neuropatología2302.11 Acidos Grasos2403 Bioquímica[EN] Alzheimer’s disease (AD) is the main cause of dementia and cognitive impairment. It has been associated with a significant diminution of omega-3 polyunsaturated fatty acid docosahexaenoic acid (DHA) levels in the brain. Clinical trials with DHA as a treatment in neurological diseases have shown inconsistent results. Previously, we reported that the presence of phytanic acid (PhA) in standard DHA compositions could be blunting DHA’s beneficial effects. Therefore, we aimed to analyze the effects of a low PhA-concentrated DHA and a standard PhA-concentrated DHA in Apolipoprotein E knockout (ApoE−/−) mice. Behavioral tests and protein expression of pro-inflammatory, pro-oxidant, antioxidant factors, and AD-related mediators were evaluated. Low PhA-concentrated DHA decreased Aβ, ß-amyloid precursor protein (APP), p-tau, Ca2+/calmodulin-dependent protein kinase II (CAMKII), caspase 3, and catalase, and increased brain derived neurotrophic factor (BDNF) when compared to standard PhA-concentrated DHA. Low PhA-concentrated DHA decreased interleukin (IL)-6 and tumor necrosis factor alpha (TNF-α) protein expression in ApoE−/− mice when compared to standard PhA-concentrated DHA. No significant differences were found in p22phox, inducible nitric oxide synthase (iNOS), glutathione peroxidase (GPx), superoxide dismutase 1 (SOD-1), and tau protein expression. The positive actions of a low PhA-concentrated DHA were functionally reflected by improving the cognitive deficit in the AD experimental model. Therefore, reduction of PhA content in DHA compositions could highlight a novel pathway for the neurodegeneration processes related to ADSIThis work was supported by grants from “Programa Estatal de Investigación, Desarrollo e Innovación Orientada a los Retos de la Sociedad, Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016” (RTC-2014-1689-1) and the Fondo de Investigación Sanitaria (Red de Trastornos Adictivos, FEDER, RD16/0017/0008 to J.A.L.M.)MDPIBiologia CelularFacultad de Ciencias Biológicas y Ambientales2019info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttps://www.mdpi.com/2072-6643/11/1/11https://hdl.handle.net/10612/24381reponame:BULERIA. Repositorio Institucional de la Universidad de Leóninstname:Universidad de LeónInglésinfo:eu-repo/grantAgreement/MINECO/Programa Estatal de I+D+I Orientada a los Retos de la Sociedad/RTC-2014-1689-1Q2818014IMADRIDinfo:eu-repo/grantAgreement/MINECO/Programa Estatal de I+D+I Orientada a los Retos de la Sociedad/RD16http://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccessoai:buleria.unileon.es:10612/243812026-06-24T12:43:27Z
dc.title.none.fl_str_mv Low Phytanic Acid-Concentrated DHA Prevents Cognitive Deficit and Regulates Alzheimer Disease Mediators in an ApoE−/− Mice Experimental Model
title Low Phytanic Acid-Concentrated DHA Prevents Cognitive Deficit and Regulates Alzheimer Disease Mediators in an ApoE−/− Mice Experimental Model
spellingShingle Low Phytanic Acid-Concentrated DHA Prevents Cognitive Deficit and Regulates Alzheimer Disease Mediators in an ApoE−/− Mice Experimental Model
Ruiz-Roso Guerra, María Belén
Bioquímica
Medicina. Salud
Alzheimer’s
DHA
ApoE -/-
Phytanic acid
Inflammation
Neuroprotection
Oxidation
3207.11 Neuropatología
2302.11 Acidos Grasos
2403 Bioquímica
title_short Low Phytanic Acid-Concentrated DHA Prevents Cognitive Deficit and Regulates Alzheimer Disease Mediators in an ApoE−/− Mice Experimental Model
title_full Low Phytanic Acid-Concentrated DHA Prevents Cognitive Deficit and Regulates Alzheimer Disease Mediators in an ApoE−/− Mice Experimental Model
title_fullStr Low Phytanic Acid-Concentrated DHA Prevents Cognitive Deficit and Regulates Alzheimer Disease Mediators in an ApoE−/− Mice Experimental Model
title_full_unstemmed Low Phytanic Acid-Concentrated DHA Prevents Cognitive Deficit and Regulates Alzheimer Disease Mediators in an ApoE−/− Mice Experimental Model
title_sort Low Phytanic Acid-Concentrated DHA Prevents Cognitive Deficit and Regulates Alzheimer Disease Mediators in an ApoE−/− Mice Experimental Model
dc.creator.none.fl_str_mv Ruiz-Roso Guerra, María Belén
Echeverry Alzate, Víctor
Ruiz-Roso Calvo de Mora, Baltasar
Quintela Fernández, José Carlos
Ballesteros Rodrigálvarez, Sandra María
Lahera Juliá, Vicente
Heras Jiménez, Natalia de las
López Moreno, José Antonio
Martín Fernández, Beatriz
author Ruiz-Roso Guerra, María Belén
author_facet Ruiz-Roso Guerra, María Belén
Echeverry Alzate, Víctor
Ruiz-Roso Calvo de Mora, Baltasar
Quintela Fernández, José Carlos
Ballesteros Rodrigálvarez, Sandra María
Lahera Juliá, Vicente
Heras Jiménez, Natalia de las
López Moreno, José Antonio
Martín Fernández, Beatriz
author_role author
author2 Echeverry Alzate, Víctor
Ruiz-Roso Calvo de Mora, Baltasar
Quintela Fernández, José Carlos
Ballesteros Rodrigálvarez, Sandra María
Lahera Juliá, Vicente
Heras Jiménez, Natalia de las
López Moreno, José Antonio
Martín Fernández, Beatriz
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Biologia Celular
Facultad de Ciencias Biológicas y Ambientales
dc.subject.none.fl_str_mv Bioquímica
Medicina. Salud
Alzheimer’s
DHA
ApoE -/-
Phytanic acid
Inflammation
Neuroprotection
Oxidation
3207.11 Neuropatología
2302.11 Acidos Grasos
2403 Bioquímica
topic Bioquímica
Medicina. Salud
Alzheimer’s
DHA
ApoE -/-
Phytanic acid
Inflammation
Neuroprotection
Oxidation
3207.11 Neuropatología
2302.11 Acidos Grasos
2403 Bioquímica
description [EN] Alzheimer’s disease (AD) is the main cause of dementia and cognitive impairment. It has been associated with a significant diminution of omega-3 polyunsaturated fatty acid docosahexaenoic acid (DHA) levels in the brain. Clinical trials with DHA as a treatment in neurological diseases have shown inconsistent results. Previously, we reported that the presence of phytanic acid (PhA) in standard DHA compositions could be blunting DHA’s beneficial effects. Therefore, we aimed to analyze the effects of a low PhA-concentrated DHA and a standard PhA-concentrated DHA in Apolipoprotein E knockout (ApoE−/−) mice. Behavioral tests and protein expression of pro-inflammatory, pro-oxidant, antioxidant factors, and AD-related mediators were evaluated. Low PhA-concentrated DHA decreased Aβ, ß-amyloid precursor protein (APP), p-tau, Ca2+/calmodulin-dependent protein kinase II (CAMKII), caspase 3, and catalase, and increased brain derived neurotrophic factor (BDNF) when compared to standard PhA-concentrated DHA. Low PhA-concentrated DHA decreased interleukin (IL)-6 and tumor necrosis factor alpha (TNF-α) protein expression in ApoE−/− mice when compared to standard PhA-concentrated DHA. No significant differences were found in p22phox, inducible nitric oxide synthase (iNOS), glutathione peroxidase (GPx), superoxide dismutase 1 (SOD-1), and tau protein expression. The positive actions of a low PhA-concentrated DHA were functionally reflected by improving the cognitive deficit in the AD experimental model. Therefore, reduction of PhA content in DHA compositions could highlight a novel pathway for the neurodegeneration processes related to AD
publishDate 2019
dc.date.none.fl_str_mv 2019
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv https://www.mdpi.com/2072-6643/11/1/11
https://hdl.handle.net/10612/24381
url https://www.mdpi.com/2072-6643/11/1/11
https://hdl.handle.net/10612/24381
dc.language.none.fl_str_mv Inglés
language_invalid_str_mv Inglés
dc.relation.none.fl_str_mv info:eu-repo/grantAgreement/MINECO/Programa Estatal de I+D+I Orientada a los Retos de la Sociedad/RTC-2014-1689-1Q2818014IMADRID
info:eu-repo/grantAgreement/MINECO/Programa Estatal de I+D+I Orientada a los Retos de la Sociedad/RD16
dc.rights.none.fl_str_mv http://creativecommons.org/licenses/by/4.0/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/4.0/
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv MDPI
publisher.none.fl_str_mv MDPI
dc.source.none.fl_str_mv reponame:BULERIA. Repositorio Institucional de la Universidad de León
instname:Universidad de León
instname_str Universidad de León
reponame_str BULERIA. Repositorio Institucional de la Universidad de León
collection BULERIA. Repositorio Institucional de la Universidad de León
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