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Brain activation in individuals suffering from bulimia nervosa and control subjects during sweet and sour taste stimuli
INTRODUCTION: Episodes of eating great quantities of extremely sweet and often aversive tasting food are a hallmark of bulimia nervosa. This unique eating pattern led researchers to seek and find differences in taste perception between patients and healthy control subjects. However, it is currently...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017461/ https://www.ncbi.nlm.nih.gov/pubmed/36937709 http://dx.doi.org/10.3389/fpsyt.2023.1022537 |
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author | Armon, Daphna Bardin Bick, Atira Florentin, Sharon Laufer, Sofia Barkai, Gabriel Bachar, Eytan Hendler, Talma Bonne, Omer Keller, Shikma |
author_facet | Armon, Daphna Bardin Bick, Atira Florentin, Sharon Laufer, Sofia Barkai, Gabriel Bachar, Eytan Hendler, Talma Bonne, Omer Keller, Shikma |
author_sort | Armon, Daphna Bardin |
collection | PubMed |
description | INTRODUCTION: Episodes of eating great quantities of extremely sweet and often aversive tasting food are a hallmark of bulimia nervosa. This unique eating pattern led researchers to seek and find differences in taste perception between patients and healthy control subjects. However, it is currently not known if these originate from central or peripheral impairment in the taste perception system. In this cross sectional study, we compare brain response to sweet and sour stimuli in 5 bulimic and 8 healthy women using functional magnetic resonance imaging (fMRI). MATERIALS AND METHODS: Sweet, sour and neutral (colorless and odorless) taste solutions were presented to subjects while undergoing fMRI scanning. Data were analyzed using a block design paradigm. RESULTS: Between-group differences in brain activation in response to both sweet and sour tastes were found in 11 brain regions, including operculum, anterior cingulate cortex, midbrain, and cerebellum. These are all considered central to perception and processing of taste. CONCLUSION: Our data propose that sweet and sour tastes may have reward or aversion eliciting attributes in patients suffering from bulimia nervosa not found in healthy subjects, suggesting that alteration in taste processing may be a core dysfunction in bulimia nervosa (BN). |
format | Online Article Text |
id | pubmed-10017461 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100174612023-03-17 Brain activation in individuals suffering from bulimia nervosa and control subjects during sweet and sour taste stimuli Armon, Daphna Bardin Bick, Atira Florentin, Sharon Laufer, Sofia Barkai, Gabriel Bachar, Eytan Hendler, Talma Bonne, Omer Keller, Shikma Front Psychiatry Psychiatry INTRODUCTION: Episodes of eating great quantities of extremely sweet and often aversive tasting food are a hallmark of bulimia nervosa. This unique eating pattern led researchers to seek and find differences in taste perception between patients and healthy control subjects. However, it is currently not known if these originate from central or peripheral impairment in the taste perception system. In this cross sectional study, we compare brain response to sweet and sour stimuli in 5 bulimic and 8 healthy women using functional magnetic resonance imaging (fMRI). MATERIALS AND METHODS: Sweet, sour and neutral (colorless and odorless) taste solutions were presented to subjects while undergoing fMRI scanning. Data were analyzed using a block design paradigm. RESULTS: Between-group differences in brain activation in response to both sweet and sour tastes were found in 11 brain regions, including operculum, anterior cingulate cortex, midbrain, and cerebellum. These are all considered central to perception and processing of taste. CONCLUSION: Our data propose that sweet and sour tastes may have reward or aversion eliciting attributes in patients suffering from bulimia nervosa not found in healthy subjects, suggesting that alteration in taste processing may be a core dysfunction in bulimia nervosa (BN). Frontiers Media S.A. 2023-03-02 /pmc/articles/PMC10017461/ /pubmed/36937709 http://dx.doi.org/10.3389/fpsyt.2023.1022537 Text en Copyright © 2023 Armon, Bick, Florentin, Laufer, Barkai, Bachar, Hendler, Bonne and Keller. https://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(s) 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 | Psychiatry Armon, Daphna Bardin Bick, Atira Florentin, Sharon Laufer, Sofia Barkai, Gabriel Bachar, Eytan Hendler, Talma Bonne, Omer Keller, Shikma Brain activation in individuals suffering from bulimia nervosa and control subjects during sweet and sour taste stimuli |
title | Brain activation in individuals suffering from bulimia nervosa and control subjects during sweet and sour taste stimuli |
title_full | Brain activation in individuals suffering from bulimia nervosa and control subjects during sweet and sour taste stimuli |
title_fullStr | Brain activation in individuals suffering from bulimia nervosa and control subjects during sweet and sour taste stimuli |
title_full_unstemmed | Brain activation in individuals suffering from bulimia nervosa and control subjects during sweet and sour taste stimuli |
title_short | Brain activation in individuals suffering from bulimia nervosa and control subjects during sweet and sour taste stimuli |
title_sort | brain activation in individuals suffering from bulimia nervosa and control subjects during sweet and sour taste stimuli |
topic | Psychiatry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017461/ https://www.ncbi.nlm.nih.gov/pubmed/36937709 http://dx.doi.org/10.3389/fpsyt.2023.1022537 |
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