Cargando…

The Gut-Brain Axis Mediates Sugar Preference

The taste of sugar is one of the most basic sensory percepts for humans and other animals. Remarkably, animals can develop a strong preference for sugar even if lacking sweet taste receptors, pointing to a mechanism independent of taste(1–3). Here we examined the neural basis for sugar preference an...

Descripción completa

Detalles Bibliográficos
Autores principales: Tan, Hwei-Ee, Sisti, Alexander C., Jin, Hao, Vignovich, Martin, Villavicencio, Miguel, Tsang, Katherine S., Goffer, Yossef, Zuker, Charles S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7185044/
https://www.ncbi.nlm.nih.gov/pubmed/32322067
http://dx.doi.org/10.1038/s41586-020-2199-7
_version_ 1783526690256846848
author Tan, Hwei-Ee
Sisti, Alexander C.
Jin, Hao
Vignovich, Martin
Villavicencio, Miguel
Tsang, Katherine S.
Goffer, Yossef
Zuker, Charles S.
author_facet Tan, Hwei-Ee
Sisti, Alexander C.
Jin, Hao
Vignovich, Martin
Villavicencio, Miguel
Tsang, Katherine S.
Goffer, Yossef
Zuker, Charles S.
author_sort Tan, Hwei-Ee
collection PubMed
description The taste of sugar is one of the most basic sensory percepts for humans and other animals. Remarkably, animals can develop a strong preference for sugar even if lacking sweet taste receptors, pointing to a mechanism independent of taste(1–3). Here we examined the neural basis for sugar preference and demonstrate that a population of neurons in the vagal ganglia and brainstem are activated via the gut-brain axis to create preference for sugar. These neurons are stimulated in response to sugar but not artificial sweeteners, and are activated by direct delivery of sugar to the gut. Using functional imaging we monitored activity of the gut-brain axis, and identified the vagal neurons activated by intestinal delivery of glucose. Next, we engineered animals where synaptic activity in this gut-to-brain circuit was genetically silenced, and prevented the development of behavioural preference for sugar. Moreover, we show that co-opting this circuit by chemogenetic activation can create preferences to un-preferred stimuli. Together, these findings reveal a gut-to-brain post-ingestive sugar-sensing pathway critical for the development of sugar preference. In addition, they explain the neural basis for differences in the behavioural effects of sweeteners versus sugar, and uncover an essential circuit underlying sugar’s highly appetitive effects.
format Online
Article
Text
id pubmed-7185044
institution National Center for Biotechnology Information
language English
publishDate 2020
record_format MEDLINE/PubMed
spelling pubmed-71850442020-10-15 The Gut-Brain Axis Mediates Sugar Preference Tan, Hwei-Ee Sisti, Alexander C. Jin, Hao Vignovich, Martin Villavicencio, Miguel Tsang, Katherine S. Goffer, Yossef Zuker, Charles S. Nature Article The taste of sugar is one of the most basic sensory percepts for humans and other animals. Remarkably, animals can develop a strong preference for sugar even if lacking sweet taste receptors, pointing to a mechanism independent of taste(1–3). Here we examined the neural basis for sugar preference and demonstrate that a population of neurons in the vagal ganglia and brainstem are activated via the gut-brain axis to create preference for sugar. These neurons are stimulated in response to sugar but not artificial sweeteners, and are activated by direct delivery of sugar to the gut. Using functional imaging we monitored activity of the gut-brain axis, and identified the vagal neurons activated by intestinal delivery of glucose. Next, we engineered animals where synaptic activity in this gut-to-brain circuit was genetically silenced, and prevented the development of behavioural preference for sugar. Moreover, we show that co-opting this circuit by chemogenetic activation can create preferences to un-preferred stimuli. Together, these findings reveal a gut-to-brain post-ingestive sugar-sensing pathway critical for the development of sugar preference. In addition, they explain the neural basis for differences in the behavioural effects of sweeteners versus sugar, and uncover an essential circuit underlying sugar’s highly appetitive effects. 2020-04-15 2020-04 /pmc/articles/PMC7185044/ /pubmed/32322067 http://dx.doi.org/10.1038/s41586-020-2199-7 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
spellingShingle Article
Tan, Hwei-Ee
Sisti, Alexander C.
Jin, Hao
Vignovich, Martin
Villavicencio, Miguel
Tsang, Katherine S.
Goffer, Yossef
Zuker, Charles S.
The Gut-Brain Axis Mediates Sugar Preference
title The Gut-Brain Axis Mediates Sugar Preference
title_full The Gut-Brain Axis Mediates Sugar Preference
title_fullStr The Gut-Brain Axis Mediates Sugar Preference
title_full_unstemmed The Gut-Brain Axis Mediates Sugar Preference
title_short The Gut-Brain Axis Mediates Sugar Preference
title_sort gut-brain axis mediates sugar preference
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7185044/
https://www.ncbi.nlm.nih.gov/pubmed/32322067
http://dx.doi.org/10.1038/s41586-020-2199-7
work_keys_str_mv AT tanhweiee thegutbrainaxismediatessugarpreference
AT sistialexanderc thegutbrainaxismediatessugarpreference
AT jinhao thegutbrainaxismediatessugarpreference
AT vignovichmartin thegutbrainaxismediatessugarpreference
AT villavicenciomiguel thegutbrainaxismediatessugarpreference
AT tsangkatherines thegutbrainaxismediatessugarpreference
AT gofferyossef thegutbrainaxismediatessugarpreference
AT zukercharless thegutbrainaxismediatessugarpreference
AT tanhweiee gutbrainaxismediatessugarpreference
AT sistialexanderc gutbrainaxismediatessugarpreference
AT jinhao gutbrainaxismediatessugarpreference
AT vignovichmartin gutbrainaxismediatessugarpreference
AT villavicenciomiguel gutbrainaxismediatessugarpreference
AT tsangkatherines gutbrainaxismediatessugarpreference
AT gofferyossef gutbrainaxismediatessugarpreference
AT zukercharless gutbrainaxismediatessugarpreference