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Chronic dietary creatine enhances hippocampal-dependent spatial memory, bioenergetics, and levels of plasticity-related proteins associated with NF-κB

The brain has a high demand for energy, of which creatine (Cr) is an important regulator. Studies document neurocognitive benefits of oral Cr in mammals, yet little is known regarding their physiological basis. This study investigated the effects of Cr supplementation (3%, w/w) on hippocampal functi...

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Autores principales: Snow, Wanda M., Cadonic, Chris, Cortes-Perez, Claudia, Roy Chowdhury, Subir K., Djordjevic, Jelena, Thomson, Ella, Bernstein, Michael J., Suh, Miyoung, Fernyhough, Paul, Albensi, Benedict C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5772392/
https://www.ncbi.nlm.nih.gov/pubmed/29339557
http://dx.doi.org/10.1101/lm.046284.117
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author Snow, Wanda M.
Cadonic, Chris
Cortes-Perez, Claudia
Roy Chowdhury, Subir K.
Djordjevic, Jelena
Thomson, Ella
Bernstein, Michael J.
Suh, Miyoung
Fernyhough, Paul
Albensi, Benedict C.
author_facet Snow, Wanda M.
Cadonic, Chris
Cortes-Perez, Claudia
Roy Chowdhury, Subir K.
Djordjevic, Jelena
Thomson, Ella
Bernstein, Michael J.
Suh, Miyoung
Fernyhough, Paul
Albensi, Benedict C.
author_sort Snow, Wanda M.
collection PubMed
description The brain has a high demand for energy, of which creatine (Cr) is an important regulator. Studies document neurocognitive benefits of oral Cr in mammals, yet little is known regarding their physiological basis. This study investigated the effects of Cr supplementation (3%, w/w) on hippocampal function in male C57BL/6 mice, including spatial learning and memory in the Morris water maze and oxygen consumption rates from isolated mitochondria in real time. Levels of transcription factors and related proteins (CREB, Egr1, and IκB to indicate NF-κB activity), proteins implicated in cognition (CaMKII, PSD-95, and Egr2), and mitochondrial proteins (electron transport chain Complex I, mitochondrial fission protein Drp1) were probed with Western blotting. Dietary Cr decreased escape latency/time to locate the platform (P < 0.05) and increased the time spent in the target quadrant (P < 0.01) in the Morris water maze. This was accompanied by increased coupled respiration (P < 0.05) in isolated hippocampal mitochondria. Protein levels of CaMKII, PSD-95, and Complex 1 were increased in Cr-fed mice, whereas IκB was decreased. These data demonstrate that dietary supplementation with Cr can improve learning, memory, and mitochondrial function and have important implications for the treatment of diseases affecting memory and energy homeostasis.
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spelling pubmed-57723922019-02-01 Chronic dietary creatine enhances hippocampal-dependent spatial memory, bioenergetics, and levels of plasticity-related proteins associated with NF-κB Snow, Wanda M. Cadonic, Chris Cortes-Perez, Claudia Roy Chowdhury, Subir K. Djordjevic, Jelena Thomson, Ella Bernstein, Michael J. Suh, Miyoung Fernyhough, Paul Albensi, Benedict C. Learn Mem Research The brain has a high demand for energy, of which creatine (Cr) is an important regulator. Studies document neurocognitive benefits of oral Cr in mammals, yet little is known regarding their physiological basis. This study investigated the effects of Cr supplementation (3%, w/w) on hippocampal function in male C57BL/6 mice, including spatial learning and memory in the Morris water maze and oxygen consumption rates from isolated mitochondria in real time. Levels of transcription factors and related proteins (CREB, Egr1, and IκB to indicate NF-κB activity), proteins implicated in cognition (CaMKII, PSD-95, and Egr2), and mitochondrial proteins (electron transport chain Complex I, mitochondrial fission protein Drp1) were probed with Western blotting. Dietary Cr decreased escape latency/time to locate the platform (P < 0.05) and increased the time spent in the target quadrant (P < 0.01) in the Morris water maze. This was accompanied by increased coupled respiration (P < 0.05) in isolated hippocampal mitochondria. Protein levels of CaMKII, PSD-95, and Complex 1 were increased in Cr-fed mice, whereas IκB was decreased. These data demonstrate that dietary supplementation with Cr can improve learning, memory, and mitochondrial function and have important implications for the treatment of diseases affecting memory and energy homeostasis. Cold Spring Harbor Laboratory Press 2018-02 /pmc/articles/PMC5772392/ /pubmed/29339557 http://dx.doi.org/10.1101/lm.046284.117 Text en © 2018 Snow et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first 12 months after the full-issue publication date (see http://learnmem.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Research
Snow, Wanda M.
Cadonic, Chris
Cortes-Perez, Claudia
Roy Chowdhury, Subir K.
Djordjevic, Jelena
Thomson, Ella
Bernstein, Michael J.
Suh, Miyoung
Fernyhough, Paul
Albensi, Benedict C.
Chronic dietary creatine enhances hippocampal-dependent spatial memory, bioenergetics, and levels of plasticity-related proteins associated with NF-κB
title Chronic dietary creatine enhances hippocampal-dependent spatial memory, bioenergetics, and levels of plasticity-related proteins associated with NF-κB
title_full Chronic dietary creatine enhances hippocampal-dependent spatial memory, bioenergetics, and levels of plasticity-related proteins associated with NF-κB
title_fullStr Chronic dietary creatine enhances hippocampal-dependent spatial memory, bioenergetics, and levels of plasticity-related proteins associated with NF-κB
title_full_unstemmed Chronic dietary creatine enhances hippocampal-dependent spatial memory, bioenergetics, and levels of plasticity-related proteins associated with NF-κB
title_short Chronic dietary creatine enhances hippocampal-dependent spatial memory, bioenergetics, and levels of plasticity-related proteins associated with NF-κB
title_sort chronic dietary creatine enhances hippocampal-dependent spatial memory, bioenergetics, and levels of plasticity-related proteins associated with nf-κb
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5772392/
https://www.ncbi.nlm.nih.gov/pubmed/29339557
http://dx.doi.org/10.1101/lm.046284.117
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