Cargando…

Thirst neurons anticipate the homeostatic consequences of eating and drinking

Thirst motivates animals to drink in order to maintain fluid balance. Traditionally, thirst has been viewed as a homeostatic response to changes in the blood volume or tonicity(1–3). However, most drinking behavior is regulated too rapidly to be controlled by blood composition directly and instead a...

Descripción completa

Detalles Bibliográficos
Autores principales: Zimmerman, Christopher A., Lin, Yen-Chu, Leib, David E., Guo, Ling, Huey, Erica L., Daly, Gwendolyn E., Chen, Yiming, Knight, Zachary A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5161740/
https://www.ncbi.nlm.nih.gov/pubmed/27487211
http://dx.doi.org/10.1038/nature18950
_version_ 1782482102957113344
author Zimmerman, Christopher A.
Lin, Yen-Chu
Leib, David E.
Guo, Ling
Huey, Erica L.
Daly, Gwendolyn E.
Chen, Yiming
Knight, Zachary A.
author_facet Zimmerman, Christopher A.
Lin, Yen-Chu
Leib, David E.
Guo, Ling
Huey, Erica L.
Daly, Gwendolyn E.
Chen, Yiming
Knight, Zachary A.
author_sort Zimmerman, Christopher A.
collection PubMed
description Thirst motivates animals to drink in order to maintain fluid balance. Traditionally, thirst has been viewed as a homeostatic response to changes in the blood volume or tonicity(1–3). However, most drinking behavior is regulated too rapidly to be controlled by blood composition directly and instead appears to anticipate homeostatic imbalances before they arise(4–11). How this is achieved remains unknown. Here we reveal an unexpected role for the subfornical organ (SFO) in the anticipatory regulation of thirst. We show by monitoring deep-brain calcium dynamics that thirst-promoting SFO neurons respond to inputs from the oral cavity during eating and drinking, which they then integrate with information about the composition of the blood. This integration allows SFO neurons to predict how ongoing food and water consumption will alter fluid balance in the future and then adjust behavior preemptively. Complementary optogenetic manipulations show that this anticipatory modulation is necessary for drinking in multiple contexts. These findings provide a neural mechanism to explain longstanding behavioral observations, including the prevalence of drinking during meals(10,11), the rapid satiation of thirst(7–9), and the fact that oral cooling is thirst-quenching(12–14).
format Online
Article
Text
id pubmed-5161740
institution National Center for Biotechnology Information
language English
publishDate 2016
record_format MEDLINE/PubMed
spelling pubmed-51617402017-02-03 Thirst neurons anticipate the homeostatic consequences of eating and drinking Zimmerman, Christopher A. Lin, Yen-Chu Leib, David E. Guo, Ling Huey, Erica L. Daly, Gwendolyn E. Chen, Yiming Knight, Zachary A. Nature Article Thirst motivates animals to drink in order to maintain fluid balance. Traditionally, thirst has been viewed as a homeostatic response to changes in the blood volume or tonicity(1–3). However, most drinking behavior is regulated too rapidly to be controlled by blood composition directly and instead appears to anticipate homeostatic imbalances before they arise(4–11). How this is achieved remains unknown. Here we reveal an unexpected role for the subfornical organ (SFO) in the anticipatory regulation of thirst. We show by monitoring deep-brain calcium dynamics that thirst-promoting SFO neurons respond to inputs from the oral cavity during eating and drinking, which they then integrate with information about the composition of the blood. This integration allows SFO neurons to predict how ongoing food and water consumption will alter fluid balance in the future and then adjust behavior preemptively. Complementary optogenetic manipulations show that this anticipatory modulation is necessary for drinking in multiple contexts. These findings provide a neural mechanism to explain longstanding behavioral observations, including the prevalence of drinking during meals(10,11), the rapid satiation of thirst(7–9), and the fact that oral cooling is thirst-quenching(12–14). 2016-08-03 2016-09-29 /pmc/articles/PMC5161740/ /pubmed/27487211 http://dx.doi.org/10.1038/nature18950 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms Reprints and permissions information is available at www.nature.com/reprints (http://www.nature.com/reprints)
spellingShingle Article
Zimmerman, Christopher A.
Lin, Yen-Chu
Leib, David E.
Guo, Ling
Huey, Erica L.
Daly, Gwendolyn E.
Chen, Yiming
Knight, Zachary A.
Thirst neurons anticipate the homeostatic consequences of eating and drinking
title Thirst neurons anticipate the homeostatic consequences of eating and drinking
title_full Thirst neurons anticipate the homeostatic consequences of eating and drinking
title_fullStr Thirst neurons anticipate the homeostatic consequences of eating and drinking
title_full_unstemmed Thirst neurons anticipate the homeostatic consequences of eating and drinking
title_short Thirst neurons anticipate the homeostatic consequences of eating and drinking
title_sort thirst neurons anticipate the homeostatic consequences of eating and drinking
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5161740/
https://www.ncbi.nlm.nih.gov/pubmed/27487211
http://dx.doi.org/10.1038/nature18950
work_keys_str_mv AT zimmermanchristophera thirstneuronsanticipatethehomeostaticconsequencesofeatinganddrinking
AT linyenchu thirstneuronsanticipatethehomeostaticconsequencesofeatinganddrinking
AT leibdavide thirstneuronsanticipatethehomeostaticconsequencesofeatinganddrinking
AT guoling thirstneuronsanticipatethehomeostaticconsequencesofeatinganddrinking
AT hueyerical thirstneuronsanticipatethehomeostaticconsequencesofeatinganddrinking
AT dalygwendolyne thirstneuronsanticipatethehomeostaticconsequencesofeatinganddrinking
AT chenyiming thirstneuronsanticipatethehomeostaticconsequencesofeatinganddrinking
AT knightzacharya thirstneuronsanticipatethehomeostaticconsequencesofeatinganddrinking