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Influence of anterior midcingulate cortex on drinking behavior during thirst and following satiation

In humans, activity in the anterior midcingulate cortex (aMCC) is associated with both subjective thirst and swallowing. This region is therefore likely to play a prominent role in the regulation of drinking in response to dehydration. Using functional MRI, we investigated this possibility during a...

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Autores principales: Saker, Pascal, Farrell, Michael J., Egan, Gary F., McKinley, Michael J., Denton, Derek A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5789944/
https://www.ncbi.nlm.nih.gov/pubmed/29311314
http://dx.doi.org/10.1073/pnas.1717646115
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author Saker, Pascal
Farrell, Michael J.
Egan, Gary F.
McKinley, Michael J.
Denton, Derek A.
author_facet Saker, Pascal
Farrell, Michael J.
Egan, Gary F.
McKinley, Michael J.
Denton, Derek A.
author_sort Saker, Pascal
collection PubMed
description In humans, activity in the anterior midcingulate cortex (aMCC) is associated with both subjective thirst and swallowing. This region is therefore likely to play a prominent role in the regulation of drinking in response to dehydration. Using functional MRI, we investigated this possibility during a period of “drinking behavior” represented by a conjunction of preswallow and swallowing events. These events were examined in the context of a thirsty condition and an “oversated” condition, the latter induced by compliant ingestion of excess fluid. Brain regions associated with swallowing showed increased activity for drinking behavior in the thirsty condition relative to the oversated condition. These regions included the cingulate cortex, premotor areas, primary sensorimotor cortices, the parietal operculum, and the supplementary motor area. Psychophysical interaction analyses revealed increased functional connectivity between the same regions and the aMCC during drinking behavior in the thirsty condition. Functional connectivity during drinking behavior was also greater for the thirsty condition relative to the oversated condition between the aMCC and two subcortical regions, the cerebellum and the rostroventral medulla, the latter containing nuclei responsible for the swallowing reflex. Finally, during drinking behavior in the oversated condition, ratings of swallowing effort showed a negative association with functional connectivity between the aMCC and two cortical regions, the sensorimotor cortex and the supramarginal gyrus. The results of this study provide evidence that the aMCC helps facilitate swallowing during a state of thirst and is therefore likely to contribute to the regulation of drinking after dehydration.
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spelling pubmed-57899442018-02-03 Influence of anterior midcingulate cortex on drinking behavior during thirst and following satiation Saker, Pascal Farrell, Michael J. Egan, Gary F. McKinley, Michael J. Denton, Derek A. Proc Natl Acad Sci U S A Biological Sciences In humans, activity in the anterior midcingulate cortex (aMCC) is associated with both subjective thirst and swallowing. This region is therefore likely to play a prominent role in the regulation of drinking in response to dehydration. Using functional MRI, we investigated this possibility during a period of “drinking behavior” represented by a conjunction of preswallow and swallowing events. These events were examined in the context of a thirsty condition and an “oversated” condition, the latter induced by compliant ingestion of excess fluid. Brain regions associated with swallowing showed increased activity for drinking behavior in the thirsty condition relative to the oversated condition. These regions included the cingulate cortex, premotor areas, primary sensorimotor cortices, the parietal operculum, and the supplementary motor area. Psychophysical interaction analyses revealed increased functional connectivity between the same regions and the aMCC during drinking behavior in the thirsty condition. Functional connectivity during drinking behavior was also greater for the thirsty condition relative to the oversated condition between the aMCC and two subcortical regions, the cerebellum and the rostroventral medulla, the latter containing nuclei responsible for the swallowing reflex. Finally, during drinking behavior in the oversated condition, ratings of swallowing effort showed a negative association with functional connectivity between the aMCC and two cortical regions, the sensorimotor cortex and the supramarginal gyrus. The results of this study provide evidence that the aMCC helps facilitate swallowing during a state of thirst and is therefore likely to contribute to the regulation of drinking after dehydration. National Academy of Sciences 2018-01-23 2018-01-08 /pmc/articles/PMC5789944/ /pubmed/29311314 http://dx.doi.org/10.1073/pnas.1717646115 Text en Copyright © 2018 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Saker, Pascal
Farrell, Michael J.
Egan, Gary F.
McKinley, Michael J.
Denton, Derek A.
Influence of anterior midcingulate cortex on drinking behavior during thirst and following satiation
title Influence of anterior midcingulate cortex on drinking behavior during thirst and following satiation
title_full Influence of anterior midcingulate cortex on drinking behavior during thirst and following satiation
title_fullStr Influence of anterior midcingulate cortex on drinking behavior during thirst and following satiation
title_full_unstemmed Influence of anterior midcingulate cortex on drinking behavior during thirst and following satiation
title_short Influence of anterior midcingulate cortex on drinking behavior during thirst and following satiation
title_sort influence of anterior midcingulate cortex on drinking behavior during thirst and following satiation
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5789944/
https://www.ncbi.nlm.nih.gov/pubmed/29311314
http://dx.doi.org/10.1073/pnas.1717646115
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