Cargando…
Inflammation-Mediated Memory Dysfunction and Effects of a Ketogenic Diet in a Murine Model of Multiple Sclerosis
A prominent clinical symptom in multiple sclerosis (MS), a progressive disorder of the central nervous system (CNS) due to heightened neuro-inflammation, is learning and memory dysfunction. Here, we investigated the effects of a ketogenic diet (KD) on memory impairment and CNS-inflammation in a muri...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342287/ https://www.ncbi.nlm.nih.gov/pubmed/22567104 http://dx.doi.org/10.1371/journal.pone.0035476 |
_version_ | 1782231673003311104 |
---|---|
author | Kim, Do Young Hao, Junwei Liu, Ruolan Turner, Gregory Shi, Fu-Dong Rho, Jong M. |
author_facet | Kim, Do Young Hao, Junwei Liu, Ruolan Turner, Gregory Shi, Fu-Dong Rho, Jong M. |
author_sort | Kim, Do Young |
collection | PubMed |
description | A prominent clinical symptom in multiple sclerosis (MS), a progressive disorder of the central nervous system (CNS) due to heightened neuro-inflammation, is learning and memory dysfunction. Here, we investigated the effects of a ketogenic diet (KD) on memory impairment and CNS-inflammation in a murine model of experimental autoimmune encephalomyelitis (EAE), using electrophysiological, behavioral, biochemical and in vivo imaging approaches. Behavioral spatial learning deficits were associated with motor disability in EAE mice, and were observed concurrently with brain inflammation. The KD improved motor disability in the EAE model, as well as CA1 hippocampal synaptic plasticity (long-term potentiation) and spatial learning and memory (assessed with the Morris Water Maze). Moreover, hippocampal atrophy and periventricular lesions in EAE mice were reversed in KD-treated EAE mice. Finally, we found that the increased expression of inflammatory cytokines and chemokines, as well as the production of reactive oxygen species (ROS), in our EAE model were both suppressed by the KD. Collectively, our findings indicate that brain inflammation in EAE mice is associated with impaired spatial learning and memory function, and that KD treatment can exert protective effects, likely via attenuation of the robust immune response and increased oxidative stress seen in these animals. |
format | Online Article Text |
id | pubmed-3342287 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33422872012-05-07 Inflammation-Mediated Memory Dysfunction and Effects of a Ketogenic Diet in a Murine Model of Multiple Sclerosis Kim, Do Young Hao, Junwei Liu, Ruolan Turner, Gregory Shi, Fu-Dong Rho, Jong M. PLoS One Research Article A prominent clinical symptom in multiple sclerosis (MS), a progressive disorder of the central nervous system (CNS) due to heightened neuro-inflammation, is learning and memory dysfunction. Here, we investigated the effects of a ketogenic diet (KD) on memory impairment and CNS-inflammation in a murine model of experimental autoimmune encephalomyelitis (EAE), using electrophysiological, behavioral, biochemical and in vivo imaging approaches. Behavioral spatial learning deficits were associated with motor disability in EAE mice, and were observed concurrently with brain inflammation. The KD improved motor disability in the EAE model, as well as CA1 hippocampal synaptic plasticity (long-term potentiation) and spatial learning and memory (assessed with the Morris Water Maze). Moreover, hippocampal atrophy and periventricular lesions in EAE mice were reversed in KD-treated EAE mice. Finally, we found that the increased expression of inflammatory cytokines and chemokines, as well as the production of reactive oxygen species (ROS), in our EAE model were both suppressed by the KD. Collectively, our findings indicate that brain inflammation in EAE mice is associated with impaired spatial learning and memory function, and that KD treatment can exert protective effects, likely via attenuation of the robust immune response and increased oxidative stress seen in these animals. Public Library of Science 2012-05-02 /pmc/articles/PMC3342287/ /pubmed/22567104 http://dx.doi.org/10.1371/journal.pone.0035476 Text en Kim et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Kim, Do Young Hao, Junwei Liu, Ruolan Turner, Gregory Shi, Fu-Dong Rho, Jong M. Inflammation-Mediated Memory Dysfunction and Effects of a Ketogenic Diet in a Murine Model of Multiple Sclerosis |
title | Inflammation-Mediated Memory Dysfunction and Effects of a Ketogenic Diet in a Murine Model of Multiple Sclerosis |
title_full | Inflammation-Mediated Memory Dysfunction and Effects of a Ketogenic Diet in a Murine Model of Multiple Sclerosis |
title_fullStr | Inflammation-Mediated Memory Dysfunction and Effects of a Ketogenic Diet in a Murine Model of Multiple Sclerosis |
title_full_unstemmed | Inflammation-Mediated Memory Dysfunction and Effects of a Ketogenic Diet in a Murine Model of Multiple Sclerosis |
title_short | Inflammation-Mediated Memory Dysfunction and Effects of a Ketogenic Diet in a Murine Model of Multiple Sclerosis |
title_sort | inflammation-mediated memory dysfunction and effects of a ketogenic diet in a murine model of multiple sclerosis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342287/ https://www.ncbi.nlm.nih.gov/pubmed/22567104 http://dx.doi.org/10.1371/journal.pone.0035476 |
work_keys_str_mv | AT kimdoyoung inflammationmediatedmemorydysfunctionandeffectsofaketogenicdietinamurinemodelofmultiplesclerosis AT haojunwei inflammationmediatedmemorydysfunctionandeffectsofaketogenicdietinamurinemodelofmultiplesclerosis AT liuruolan inflammationmediatedmemorydysfunctionandeffectsofaketogenicdietinamurinemodelofmultiplesclerosis AT turnergregory inflammationmediatedmemorydysfunctionandeffectsofaketogenicdietinamurinemodelofmultiplesclerosis AT shifudong inflammationmediatedmemorydysfunctionandeffectsofaketogenicdietinamurinemodelofmultiplesclerosis AT rhojongm inflammationmediatedmemorydysfunctionandeffectsofaketogenicdietinamurinemodelofmultiplesclerosis |