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Interplay Between the Gut-Brain Axis, Obesity and Cognitive Function

Obesity continues to be one of the major public health problems due to its high prevalence and co-morbidities. Common co-morbidities not only include cardiometabolic disorders but also mood and cognitive disorders. Obese subjects often show deficits in memory, learning and executive functions compar...

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Autores principales: Agustí, Ana, García-Pardo, Maria P., López-Almela, Inmaculada, Campillo, Isabel, Maes, Michael, Romaní-Pérez, Marina, Sanz, Yolanda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5864897/
https://www.ncbi.nlm.nih.gov/pubmed/29615850
http://dx.doi.org/10.3389/fnins.2018.00155
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author Agustí, Ana
García-Pardo, Maria P.
López-Almela, Inmaculada
Campillo, Isabel
Maes, Michael
Romaní-Pérez, Marina
Sanz, Yolanda
author_facet Agustí, Ana
García-Pardo, Maria P.
López-Almela, Inmaculada
Campillo, Isabel
Maes, Michael
Romaní-Pérez, Marina
Sanz, Yolanda
author_sort Agustí, Ana
collection PubMed
description Obesity continues to be one of the major public health problems due to its high prevalence and co-morbidities. Common co-morbidities not only include cardiometabolic disorders but also mood and cognitive disorders. Obese subjects often show deficits in memory, learning and executive functions compared to normal weight subjects. Epidemiological studies also indicate that obesity is associated with a higher risk of developing depression and anxiety, and vice versa. These associations between pathologies that presumably have different etiologies suggest shared pathological mechanisms. Gut microbiota is a mediating factor between the environmental pressures (e.g., diet, lifestyle) and host physiology, and its alteration could partly explain the cross-link between those pathologies. Westernized dietary patterns are known to be a major cause of the obesity epidemic, which also promotes a dysbiotic drift in the gut microbiota; this, in turn, seems to contribute to obesity-related complications. Experimental studies in animal models and, to a lesser extent, in humans suggest that the obesity-associated microbiota may contribute to the endocrine, neurochemical and inflammatory alterations underlying obesity and its comorbidities. These include dysregulation of the HPA-axis with overproduction of glucocorticoids, alterations in levels of neuroactive metabolites (e.g., neurotransmitters, short-chain fatty acids) and activation of a pro-inflammatory milieu that can cause neuro-inflammation. This review updates current knowledge about the role and mode of action of the gut microbiota in the cross-link between energy metabolism, mood and cognitive function.
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spelling pubmed-58648972018-04-03 Interplay Between the Gut-Brain Axis, Obesity and Cognitive Function Agustí, Ana García-Pardo, Maria P. López-Almela, Inmaculada Campillo, Isabel Maes, Michael Romaní-Pérez, Marina Sanz, Yolanda Front Neurosci Neuroscience Obesity continues to be one of the major public health problems due to its high prevalence and co-morbidities. Common co-morbidities not only include cardiometabolic disorders but also mood and cognitive disorders. Obese subjects often show deficits in memory, learning and executive functions compared to normal weight subjects. Epidemiological studies also indicate that obesity is associated with a higher risk of developing depression and anxiety, and vice versa. These associations between pathologies that presumably have different etiologies suggest shared pathological mechanisms. Gut microbiota is a mediating factor between the environmental pressures (e.g., diet, lifestyle) and host physiology, and its alteration could partly explain the cross-link between those pathologies. Westernized dietary patterns are known to be a major cause of the obesity epidemic, which also promotes a dysbiotic drift in the gut microbiota; this, in turn, seems to contribute to obesity-related complications. Experimental studies in animal models and, to a lesser extent, in humans suggest that the obesity-associated microbiota may contribute to the endocrine, neurochemical and inflammatory alterations underlying obesity and its comorbidities. These include dysregulation of the HPA-axis with overproduction of glucocorticoids, alterations in levels of neuroactive metabolites (e.g., neurotransmitters, short-chain fatty acids) and activation of a pro-inflammatory milieu that can cause neuro-inflammation. This review updates current knowledge about the role and mode of action of the gut microbiota in the cross-link between energy metabolism, mood and cognitive function. Frontiers Media S.A. 2018-03-16 /pmc/articles/PMC5864897/ /pubmed/29615850 http://dx.doi.org/10.3389/fnins.2018.00155 Text en Copyright © 2018 Agustí, García-Pardo, López-Almela, Campillo, Maes, Romaní-Pérez and Sanz. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Agustí, Ana
García-Pardo, Maria P.
López-Almela, Inmaculada
Campillo, Isabel
Maes, Michael
Romaní-Pérez, Marina
Sanz, Yolanda
Interplay Between the Gut-Brain Axis, Obesity and Cognitive Function
title Interplay Between the Gut-Brain Axis, Obesity and Cognitive Function
title_full Interplay Between the Gut-Brain Axis, Obesity and Cognitive Function
title_fullStr Interplay Between the Gut-Brain Axis, Obesity and Cognitive Function
title_full_unstemmed Interplay Between the Gut-Brain Axis, Obesity and Cognitive Function
title_short Interplay Between the Gut-Brain Axis, Obesity and Cognitive Function
title_sort interplay between the gut-brain axis, obesity and cognitive function
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5864897/
https://www.ncbi.nlm.nih.gov/pubmed/29615850
http://dx.doi.org/10.3389/fnins.2018.00155
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