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Behavioral dissection of hunger states in Drosophila
Hunger is a motivational drive that promotes feeding, and it can be generated by the physiological need to consume nutrients as well as the hedonic properties of food. Brain circuits and mechanisms that regulate feeding have been described, but which of these contribute to the generation of motive f...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10328523/ https://www.ncbi.nlm.nih.gov/pubmed/37326496 http://dx.doi.org/10.7554/eLife.84537 |
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author | Weaver, Kristina J Raju, Sonakshi Rucker, Rachel A Chakraborty, Tuhin Holt, Robert A Pletcher, Scott D |
author_facet | Weaver, Kristina J Raju, Sonakshi Rucker, Rachel A Chakraborty, Tuhin Holt, Robert A Pletcher, Scott D |
author_sort | Weaver, Kristina J |
collection | PubMed |
description | Hunger is a motivational drive that promotes feeding, and it can be generated by the physiological need to consume nutrients as well as the hedonic properties of food. Brain circuits and mechanisms that regulate feeding have been described, but which of these contribute to the generation of motive forces that drive feeding is unclear. Here, we describe our first efforts at behaviorally and neuronally distinguishing hedonic from homeostatic hunger states in Drosophila melanogaster and propose that this system can be used as a model to dissect the molecular mechanisms that underlie feeding motivation. We visually identify and quantify behaviors exhibited by hungry flies and find that increased feeding duration is a behavioral signature of hedonic feeding motivation. Using a genetically encoded marker of neuronal activity, we find that the mushroom body (MB) lobes are activated by hedonic food environments, and we use optogenetic inhibition to implicate a dopaminergic neuron cluster (protocerebral anterior medial [PAM]) to α’/β’ MB circuit in hedonic feeding motivation. The identification of discrete hunger states in flies and the development of behavioral assays to measure them offers a framework to begin dissecting the molecular and circuit mechanisms that generate motivational states in the brain. |
format | Online Article Text |
id | pubmed-10328523 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-103285232023-07-08 Behavioral dissection of hunger states in Drosophila Weaver, Kristina J Raju, Sonakshi Rucker, Rachel A Chakraborty, Tuhin Holt, Robert A Pletcher, Scott D eLife Genetics and Genomics Hunger is a motivational drive that promotes feeding, and it can be generated by the physiological need to consume nutrients as well as the hedonic properties of food. Brain circuits and mechanisms that regulate feeding have been described, but which of these contribute to the generation of motive forces that drive feeding is unclear. Here, we describe our first efforts at behaviorally and neuronally distinguishing hedonic from homeostatic hunger states in Drosophila melanogaster and propose that this system can be used as a model to dissect the molecular mechanisms that underlie feeding motivation. We visually identify and quantify behaviors exhibited by hungry flies and find that increased feeding duration is a behavioral signature of hedonic feeding motivation. Using a genetically encoded marker of neuronal activity, we find that the mushroom body (MB) lobes are activated by hedonic food environments, and we use optogenetic inhibition to implicate a dopaminergic neuron cluster (protocerebral anterior medial [PAM]) to α’/β’ MB circuit in hedonic feeding motivation. The identification of discrete hunger states in flies and the development of behavioral assays to measure them offers a framework to begin dissecting the molecular and circuit mechanisms that generate motivational states in the brain. eLife Sciences Publications, Ltd 2023-06-16 /pmc/articles/PMC10328523/ /pubmed/37326496 http://dx.doi.org/10.7554/eLife.84537 Text en © 2023, Weaver et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Genetics and Genomics Weaver, Kristina J Raju, Sonakshi Rucker, Rachel A Chakraborty, Tuhin Holt, Robert A Pletcher, Scott D Behavioral dissection of hunger states in Drosophila |
title | Behavioral dissection of hunger states in Drosophila |
title_full | Behavioral dissection of hunger states in Drosophila |
title_fullStr | Behavioral dissection of hunger states in Drosophila |
title_full_unstemmed | Behavioral dissection of hunger states in Drosophila |
title_short | Behavioral dissection of hunger states in Drosophila |
title_sort | behavioral dissection of hunger states in drosophila |
topic | Genetics and Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10328523/ https://www.ncbi.nlm.nih.gov/pubmed/37326496 http://dx.doi.org/10.7554/eLife.84537 |
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