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Temporally specific engagement of distinct neuronal circuits regulating olfactory habituation in Drosophila

Habituation is the process that enables salience filtering, precipitating perceptual changes that alter the value of environmental stimuli. To discern the neuronal circuits underlying habituation to brief inconsequential stimuli, we developed a novel olfactory habituation paradigm, identifying two d...

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Detalles Bibliográficos
Autores principales: Semelidou, Ourania, Acevedo, Summer F, Skoulakis, Efthimios MC
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303106/
https://www.ncbi.nlm.nih.gov/pubmed/30576281
http://dx.doi.org/10.7554/eLife.39569
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author Semelidou, Ourania
Acevedo, Summer F
Skoulakis, Efthimios MC
author_facet Semelidou, Ourania
Acevedo, Summer F
Skoulakis, Efthimios MC
author_sort Semelidou, Ourania
collection PubMed
description Habituation is the process that enables salience filtering, precipitating perceptual changes that alter the value of environmental stimuli. To discern the neuronal circuits underlying habituation to brief inconsequential stimuli, we developed a novel olfactory habituation paradigm, identifying two distinct phases of the response that engage distinct neuronal circuits. Responsiveness to the continuous odor stimulus is maintained initially, a phase we term habituation latency and requires Rutabaga Adenylyl-Cyclase-depended neurotransmission from GABAergic Antennal Lobe Interneurons and activation of excitatory Projection Neurons (PNs) and the Mushroom Bodies. In contrast, habituation depends on the inhibitory PNs of the middle Antenno-Cerebral Track, requires inner Antenno-Cerebral Track PN activation and defines a temporally distinct phase. Collectively, our data support the involvement of Lateral Horn excitatory and inhibitory stimulation in habituation. These results provide essential cellular substrates for future analyses of the molecular mechanisms that govern the duration and transition between these distinct temporal habituation phases. Editorial note: This article has been through an editorial process in which the authors decide how to respond to the issues raised during peer review. The Reviewing Editor's assessment is that all the issues have been addressed (see decision letter).
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spelling pubmed-63031062019-01-04 Temporally specific engagement of distinct neuronal circuits regulating olfactory habituation in Drosophila Semelidou, Ourania Acevedo, Summer F Skoulakis, Efthimios MC eLife Neuroscience Habituation is the process that enables salience filtering, precipitating perceptual changes that alter the value of environmental stimuli. To discern the neuronal circuits underlying habituation to brief inconsequential stimuli, we developed a novel olfactory habituation paradigm, identifying two distinct phases of the response that engage distinct neuronal circuits. Responsiveness to the continuous odor stimulus is maintained initially, a phase we term habituation latency and requires Rutabaga Adenylyl-Cyclase-depended neurotransmission from GABAergic Antennal Lobe Interneurons and activation of excitatory Projection Neurons (PNs) and the Mushroom Bodies. In contrast, habituation depends on the inhibitory PNs of the middle Antenno-Cerebral Track, requires inner Antenno-Cerebral Track PN activation and defines a temporally distinct phase. Collectively, our data support the involvement of Lateral Horn excitatory and inhibitory stimulation in habituation. These results provide essential cellular substrates for future analyses of the molecular mechanisms that govern the duration and transition between these distinct temporal habituation phases. Editorial note: This article has been through an editorial process in which the authors decide how to respond to the issues raised during peer review. The Reviewing Editor's assessment is that all the issues have been addressed (see decision letter). eLife Sciences Publications, Ltd 2018-12-21 /pmc/articles/PMC6303106/ /pubmed/30576281 http://dx.doi.org/10.7554/eLife.39569 Text en © 2018, Semelidou et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Semelidou, Ourania
Acevedo, Summer F
Skoulakis, Efthimios MC
Temporally specific engagement of distinct neuronal circuits regulating olfactory habituation in Drosophila
title Temporally specific engagement of distinct neuronal circuits regulating olfactory habituation in Drosophila
title_full Temporally specific engagement of distinct neuronal circuits regulating olfactory habituation in Drosophila
title_fullStr Temporally specific engagement of distinct neuronal circuits regulating olfactory habituation in Drosophila
title_full_unstemmed Temporally specific engagement of distinct neuronal circuits regulating olfactory habituation in Drosophila
title_short Temporally specific engagement of distinct neuronal circuits regulating olfactory habituation in Drosophila
title_sort temporally specific engagement of distinct neuronal circuits regulating olfactory habituation in drosophila
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303106/
https://www.ncbi.nlm.nih.gov/pubmed/30576281
http://dx.doi.org/10.7554/eLife.39569
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