Cargando…
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...
Autores principales: | , , , , , , , , , |
---|---|
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 |
_version_ | 1783293404850946048 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5772392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT snowwandam chronicdietarycreatineenhanceshippocampaldependentspatialmemorybioenergeticsandlevelsofplasticityrelatedproteinsassociatedwithnfkb AT cadonicchris chronicdietarycreatineenhanceshippocampaldependentspatialmemorybioenergeticsandlevelsofplasticityrelatedproteinsassociatedwithnfkb AT cortesperezclaudia chronicdietarycreatineenhanceshippocampaldependentspatialmemorybioenergeticsandlevelsofplasticityrelatedproteinsassociatedwithnfkb AT roychowdhurysubirk chronicdietarycreatineenhanceshippocampaldependentspatialmemorybioenergeticsandlevelsofplasticityrelatedproteinsassociatedwithnfkb AT djordjevicjelena chronicdietarycreatineenhanceshippocampaldependentspatialmemorybioenergeticsandlevelsofplasticityrelatedproteinsassociatedwithnfkb AT thomsonella chronicdietarycreatineenhanceshippocampaldependentspatialmemorybioenergeticsandlevelsofplasticityrelatedproteinsassociatedwithnfkb AT bernsteinmichaelj chronicdietarycreatineenhanceshippocampaldependentspatialmemorybioenergeticsandlevelsofplasticityrelatedproteinsassociatedwithnfkb AT suhmiyoung chronicdietarycreatineenhanceshippocampaldependentspatialmemorybioenergeticsandlevelsofplasticityrelatedproteinsassociatedwithnfkb AT fernyhoughpaul chronicdietarycreatineenhanceshippocampaldependentspatialmemorybioenergeticsandlevelsofplasticityrelatedproteinsassociatedwithnfkb AT albensibenedictc chronicdietarycreatineenhanceshippocampaldependentspatialmemorybioenergeticsandlevelsofplasticityrelatedproteinsassociatedwithnfkb |