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Taste cues elicit prolonged modulation of feeding behavior in Drosophila

Taste cues regulate immediate feeding behavior, but their ability to modulate future behavior has been less well studied. Pairing one taste with another can modulate subsequent feeding responses through associative learning, but this requires simultaneous exposure to both stimuli. We investigated wh...

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Detalles Bibliográficos
Autores principales: Deere, Julia U., Devineni, Anita V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9529979/
https://www.ncbi.nlm.nih.gov/pubmed/36204264
http://dx.doi.org/10.1016/j.isci.2022.105159
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author Deere, Julia U.
Devineni, Anita V.
author_facet Deere, Julia U.
Devineni, Anita V.
author_sort Deere, Julia U.
collection PubMed
description Taste cues regulate immediate feeding behavior, but their ability to modulate future behavior has been less well studied. Pairing one taste with another can modulate subsequent feeding responses through associative learning, but this requires simultaneous exposure to both stimuli. We investigated whether exposure to one taste modulates future responses to other tastes even when they do not overlap in time. Using Drosophila, we found that brief exposure to sugar enhanced future feeding responses, whereas bitter exposure suppressed them. This modulation relies on neural pathways distinct from those that acutely regulate feeding or mediate learning-dependent changes. Sensory neuron activity was required not only during initial taste exposure but also afterward, suggesting that ongoing sensory activity may maintain experience-dependent changes in downstream circuits. Thus, the brain stores a memory of each taste stimulus after it disappears, enabling animals to integrate information as they sequentially sample different taste cues that signal local food quality.
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spelling pubmed-95299792022-10-05 Taste cues elicit prolonged modulation of feeding behavior in Drosophila Deere, Julia U. Devineni, Anita V. iScience Article Taste cues regulate immediate feeding behavior, but their ability to modulate future behavior has been less well studied. Pairing one taste with another can modulate subsequent feeding responses through associative learning, but this requires simultaneous exposure to both stimuli. We investigated whether exposure to one taste modulates future responses to other tastes even when they do not overlap in time. Using Drosophila, we found that brief exposure to sugar enhanced future feeding responses, whereas bitter exposure suppressed them. This modulation relies on neural pathways distinct from those that acutely regulate feeding or mediate learning-dependent changes. Sensory neuron activity was required not only during initial taste exposure but also afterward, suggesting that ongoing sensory activity may maintain experience-dependent changes in downstream circuits. Thus, the brain stores a memory of each taste stimulus after it disappears, enabling animals to integrate information as they sequentially sample different taste cues that signal local food quality. Elsevier 2022-09-17 /pmc/articles/PMC9529979/ /pubmed/36204264 http://dx.doi.org/10.1016/j.isci.2022.105159 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Deere, Julia U.
Devineni, Anita V.
Taste cues elicit prolonged modulation of feeding behavior in Drosophila
title Taste cues elicit prolonged modulation of feeding behavior in Drosophila
title_full Taste cues elicit prolonged modulation of feeding behavior in Drosophila
title_fullStr Taste cues elicit prolonged modulation of feeding behavior in Drosophila
title_full_unstemmed Taste cues elicit prolonged modulation of feeding behavior in Drosophila
title_short Taste cues elicit prolonged modulation of feeding behavior in Drosophila
title_sort taste cues elicit prolonged modulation of feeding behavior in drosophila
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9529979/
https://www.ncbi.nlm.nih.gov/pubmed/36204264
http://dx.doi.org/10.1016/j.isci.2022.105159
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