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Effects of individual glucose levels on the neuronal correlates of emotions

This study aimed to directly assess the effect of changes in blood glucose levels on the psychological processing of emotionally charged material. We used functional magnetic resonance imaging (fMRI) to evaluate the effect of blood glucose levels on three categories of visually presented emotional s...

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Autores principales: Schöpf, Veronika, Fischmeister, Florian Ph. S., Windischberger, Christian, Gerstl, Florian, Wolzt, Michael, Karlsson, Karl Æ., Moser, Ewald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3659280/
https://www.ncbi.nlm.nih.gov/pubmed/23734117
http://dx.doi.org/10.3389/fnhum.2013.00212
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author Schöpf, Veronika
Fischmeister, Florian Ph. S.
Windischberger, Christian
Gerstl, Florian
Wolzt, Michael
Karlsson, Karl Æ.
Moser, Ewald
author_facet Schöpf, Veronika
Fischmeister, Florian Ph. S.
Windischberger, Christian
Gerstl, Florian
Wolzt, Michael
Karlsson, Karl Æ.
Moser, Ewald
author_sort Schöpf, Veronika
collection PubMed
description This study aimed to directly assess the effect of changes in blood glucose levels on the psychological processing of emotionally charged material. We used functional magnetic resonance imaging (fMRI) to evaluate the effect of blood glucose levels on three categories of visually presented emotional stimuli. Seventeen healthy young subjects participated in this study (eight females; nine males; body weight, 69.3 ± 14.9 kg; BMI, 22 ± 2.7; age, 24 ± 3 years), consisting of two functional MRI sessions: (1) after an overnight fast under resting conditions (before glucose administration); (2) after reaching the hyperglycemic state (after glucose administration). During each session, subjects were presented with visual stimuli featuring funny, neutral, and sad content. Single-subject ratings of the stimuli were used to verify the selection of stimuli for each category and were covariates for the fMRI analysis. Analysis of the interaction effect of the two sessions (eu- and hyperglycemia), and the emotional categories accounting for the single-subject glucose differences, revealed a single activation cluster in the hypothalamus. Analysis of the activation profile of the left amygdala corresponded to the three emotional conditions, and this profile was obtained for both sessions regardless of glucose level. Our results indicate that, in a hyperglycemic state, the hypothalamus can no longer respond to emotions. This study offers novel insight for the understanding of disease-related behavior associated with dysregulation of glucose and glucose availability, potentially offering improved diagnostic and novel therapeutic strategies in the future.
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spelling pubmed-36592802013-06-03 Effects of individual glucose levels on the neuronal correlates of emotions Schöpf, Veronika Fischmeister, Florian Ph. S. Windischberger, Christian Gerstl, Florian Wolzt, Michael Karlsson, Karl Æ. Moser, Ewald Front Hum Neurosci Neuroscience This study aimed to directly assess the effect of changes in blood glucose levels on the psychological processing of emotionally charged material. We used functional magnetic resonance imaging (fMRI) to evaluate the effect of blood glucose levels on three categories of visually presented emotional stimuli. Seventeen healthy young subjects participated in this study (eight females; nine males; body weight, 69.3 ± 14.9 kg; BMI, 22 ± 2.7; age, 24 ± 3 years), consisting of two functional MRI sessions: (1) after an overnight fast under resting conditions (before glucose administration); (2) after reaching the hyperglycemic state (after glucose administration). During each session, subjects were presented with visual stimuli featuring funny, neutral, and sad content. Single-subject ratings of the stimuli were used to verify the selection of stimuli for each category and were covariates for the fMRI analysis. Analysis of the interaction effect of the two sessions (eu- and hyperglycemia), and the emotional categories accounting for the single-subject glucose differences, revealed a single activation cluster in the hypothalamus. Analysis of the activation profile of the left amygdala corresponded to the three emotional conditions, and this profile was obtained for both sessions regardless of glucose level. Our results indicate that, in a hyperglycemic state, the hypothalamus can no longer respond to emotions. This study offers novel insight for the understanding of disease-related behavior associated with dysregulation of glucose and glucose availability, potentially offering improved diagnostic and novel therapeutic strategies in the future. Frontiers Media S.A. 2013-05-21 /pmc/articles/PMC3659280/ /pubmed/23734117 http://dx.doi.org/10.3389/fnhum.2013.00212 Text en Copyright © 2013 Schöpf, Fischmeister, Windischberger, Gerstl, Wolzt, Karlsson and Moser. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Neuroscience
Schöpf, Veronika
Fischmeister, Florian Ph. S.
Windischberger, Christian
Gerstl, Florian
Wolzt, Michael
Karlsson, Karl Æ.
Moser, Ewald
Effects of individual glucose levels on the neuronal correlates of emotions
title Effects of individual glucose levels on the neuronal correlates of emotions
title_full Effects of individual glucose levels on the neuronal correlates of emotions
title_fullStr Effects of individual glucose levels on the neuronal correlates of emotions
title_full_unstemmed Effects of individual glucose levels on the neuronal correlates of emotions
title_short Effects of individual glucose levels on the neuronal correlates of emotions
title_sort effects of individual glucose levels on the neuronal correlates of emotions
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3659280/
https://www.ncbi.nlm.nih.gov/pubmed/23734117
http://dx.doi.org/10.3389/fnhum.2013.00212
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