Cargando…

A Drosophila ex vivo model of olfactory appetitive learning

During olfactory appetitive learning, animals associate an odor, or conditioned stimulus (CS), with an unconditioned stimulus (US), often a sugar reward. This association induces feeding behavior, a conditioned response (CR), upon subsequent exposure to the CS. In this study, we developed a model of...

Descripción completa

Detalles Bibliográficos
Autores principales: Suzuki-Sawano, Ema, Ueno, Kohei, Naganos, Shintaro, Sawano, Yoshihiro, Horiuchi, Junjiro, Saitoe, Minoru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5735177/
https://www.ncbi.nlm.nih.gov/pubmed/29255174
http://dx.doi.org/10.1038/s41598-017-17955-1
_version_ 1783287152681943040
author Suzuki-Sawano, Ema
Ueno, Kohei
Naganos, Shintaro
Sawano, Yoshihiro
Horiuchi, Junjiro
Saitoe, Minoru
author_facet Suzuki-Sawano, Ema
Ueno, Kohei
Naganos, Shintaro
Sawano, Yoshihiro
Horiuchi, Junjiro
Saitoe, Minoru
author_sort Suzuki-Sawano, Ema
collection PubMed
description During olfactory appetitive learning, animals associate an odor, or conditioned stimulus (CS), with an unconditioned stimulus (US), often a sugar reward. This association induces feeding behavior, a conditioned response (CR), upon subsequent exposure to the CS. In this study, we developed a model of this behavior in isolated Drosophila brains. Artificial activation of neurons expressing the Gr5a sugar-responsive gustatory receptor (Gr5a GRNs) induces feeding behavior in starved flies. Consistent with this, we find that in dissected brains, activation of Gr5a GRNs induces Ca(2+) transients in motor neurons, MN11 + 12, required for ingestion. Significantly, activation of Gr5a GRNs can substitute for presentation of sugar rewards during olfactory appetitive learning. Similarly, in dissected brains, coincident stimulation of Gr5a GRNs and the antennal lobe (AL), which processes olfactory information, results in increased Ca(2+) influx into MN11 + 12 cells upon subsequent AL stimulation. Importantly, olfactory appetitive associations are not formed in satiated flies. Likewise, AL-evoked Ca(2+) transients in MN11 + 12 are not produced in ex vivo brains from satiated flies. Our results suggest that a starved/satiated state is maintained in dissected brains, and that this ex vivo system will be useful for identification of neural networks involved in olfactory appetitive learning.
format Online
Article
Text
id pubmed-5735177
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-57351772017-12-21 A Drosophila ex vivo model of olfactory appetitive learning Suzuki-Sawano, Ema Ueno, Kohei Naganos, Shintaro Sawano, Yoshihiro Horiuchi, Junjiro Saitoe, Minoru Sci Rep Article During olfactory appetitive learning, animals associate an odor, or conditioned stimulus (CS), with an unconditioned stimulus (US), often a sugar reward. This association induces feeding behavior, a conditioned response (CR), upon subsequent exposure to the CS. In this study, we developed a model of this behavior in isolated Drosophila brains. Artificial activation of neurons expressing the Gr5a sugar-responsive gustatory receptor (Gr5a GRNs) induces feeding behavior in starved flies. Consistent with this, we find that in dissected brains, activation of Gr5a GRNs induces Ca(2+) transients in motor neurons, MN11 + 12, required for ingestion. Significantly, activation of Gr5a GRNs can substitute for presentation of sugar rewards during olfactory appetitive learning. Similarly, in dissected brains, coincident stimulation of Gr5a GRNs and the antennal lobe (AL), which processes olfactory information, results in increased Ca(2+) influx into MN11 + 12 cells upon subsequent AL stimulation. Importantly, olfactory appetitive associations are not formed in satiated flies. Likewise, AL-evoked Ca(2+) transients in MN11 + 12 are not produced in ex vivo brains from satiated flies. Our results suggest that a starved/satiated state is maintained in dissected brains, and that this ex vivo system will be useful for identification of neural networks involved in olfactory appetitive learning. Nature Publishing Group UK 2017-12-18 /pmc/articles/PMC5735177/ /pubmed/29255174 http://dx.doi.org/10.1038/s41598-017-17955-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Suzuki-Sawano, Ema
Ueno, Kohei
Naganos, Shintaro
Sawano, Yoshihiro
Horiuchi, Junjiro
Saitoe, Minoru
A Drosophila ex vivo model of olfactory appetitive learning
title A Drosophila ex vivo model of olfactory appetitive learning
title_full A Drosophila ex vivo model of olfactory appetitive learning
title_fullStr A Drosophila ex vivo model of olfactory appetitive learning
title_full_unstemmed A Drosophila ex vivo model of olfactory appetitive learning
title_short A Drosophila ex vivo model of olfactory appetitive learning
title_sort drosophila ex vivo model of olfactory appetitive learning
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5735177/
https://www.ncbi.nlm.nih.gov/pubmed/29255174
http://dx.doi.org/10.1038/s41598-017-17955-1
work_keys_str_mv AT suzukisawanoema adrosophilaexvivomodelofolfactoryappetitivelearning
AT uenokohei adrosophilaexvivomodelofolfactoryappetitivelearning
AT naganosshintaro adrosophilaexvivomodelofolfactoryappetitivelearning
AT sawanoyoshihiro adrosophilaexvivomodelofolfactoryappetitivelearning
AT horiuchijunjiro adrosophilaexvivomodelofolfactoryappetitivelearning
AT saitoeminoru adrosophilaexvivomodelofolfactoryappetitivelearning
AT suzukisawanoema drosophilaexvivomodelofolfactoryappetitivelearning
AT uenokohei drosophilaexvivomodelofolfactoryappetitivelearning
AT naganosshintaro drosophilaexvivomodelofolfactoryappetitivelearning
AT sawanoyoshihiro drosophilaexvivomodelofolfactoryappetitivelearning
AT horiuchijunjiro drosophilaexvivomodelofolfactoryappetitivelearning
AT saitoeminoru drosophilaexvivomodelofolfactoryappetitivelearning