Muscarinic ACh Receptors Contribute to Aversive Olfactory Learning in Drosophila

The most studied form of associative learning in Drosophila consists in pairing an odorant, the conditioned stimulus (CS), with an unconditioned stimulus (US). The timely arrival of the CS and US information to a specific Drosophila brain association region, the mushroom bodies (MB), can induce new...

Full description

Saved in:
Bibliographic Details
Main Authors: Bryon Silva, Claudia Molina-Fernández, María Beatriz Ugalde, Eduardo I. Tognarelli, Cristian Angel, Jorge M. Campusano
Format: Article
Language:English
Published: Wiley 2015-01-01
Series:Neural Plasticity
Online Access:http://dx.doi.org/10.1155/2015/658918
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832566857902587904
author Bryon Silva
Claudia Molina-Fernández
María Beatriz Ugalde
Eduardo I. Tognarelli
Cristian Angel
Jorge M. Campusano
author_facet Bryon Silva
Claudia Molina-Fernández
María Beatriz Ugalde
Eduardo I. Tognarelli
Cristian Angel
Jorge M. Campusano
author_sort Bryon Silva
collection DOAJ
description The most studied form of associative learning in Drosophila consists in pairing an odorant, the conditioned stimulus (CS), with an unconditioned stimulus (US). The timely arrival of the CS and US information to a specific Drosophila brain association region, the mushroom bodies (MB), can induce new olfactory memories. Thus, the MB is considered a coincidence detector. It has been shown that olfactory information is conveyed to the MB through cholinergic inputs that activate acetylcholine (ACh) receptors, while the US is encoded by biogenic amine (BA) systems. In recent years, we have advanced our understanding on the specific neural BA pathways and receptors involved in olfactory learning and memory. However, little information exists on the contribution of cholinergic receptors to this process. Here we evaluate for the first time the proposition that, as in mammals, muscarinic ACh receptors (mAChRs) contribute to memory formation in Drosophila. Our results show that pharmacological and genetic blockade of mAChRs in MB disrupts olfactory aversive memory in larvae. This effect is not explained by an alteration in the ability of animals to respond to odorants or to execute motor programs. These results show that mAChRs in MB contribute to generating olfactory memories in Drosophila.
format Article
id doaj-art-d66b2bd45cf14315a33c95b3c490f4b8
institution Kabale University
issn 2090-5904
1687-5443
language English
publishDate 2015-01-01
publisher Wiley
record_format Article
series Neural Plasticity
spelling doaj-art-d66b2bd45cf14315a33c95b3c490f4b82025-02-03T01:03:02ZengWileyNeural Plasticity2090-59041687-54432015-01-01201510.1155/2015/658918658918Muscarinic ACh Receptors Contribute to Aversive Olfactory Learning in DrosophilaBryon Silva0Claudia Molina-Fernández1María Beatriz Ugalde2Eduardo I. Tognarelli3Cristian Angel4Jorge M. Campusano5Laboratorio Neurogenética de la Conducta, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Alameda 340, 8331150 Santiago, ChileLaboratorio Neurogenética de la Conducta, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Alameda 340, 8331150 Santiago, ChileLaboratorio Neurogenética de la Conducta, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Alameda 340, 8331150 Santiago, ChileLaboratorio Neurogenética de la Conducta, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Alameda 340, 8331150 Santiago, ChileLaboratorio Neurogenética de la Conducta, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Alameda 340, 8331150 Santiago, ChileLaboratorio Neurogenética de la Conducta, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Alameda 340, 8331150 Santiago, ChileThe most studied form of associative learning in Drosophila consists in pairing an odorant, the conditioned stimulus (CS), with an unconditioned stimulus (US). The timely arrival of the CS and US information to a specific Drosophila brain association region, the mushroom bodies (MB), can induce new olfactory memories. Thus, the MB is considered a coincidence detector. It has been shown that olfactory information is conveyed to the MB through cholinergic inputs that activate acetylcholine (ACh) receptors, while the US is encoded by biogenic amine (BA) systems. In recent years, we have advanced our understanding on the specific neural BA pathways and receptors involved in olfactory learning and memory. However, little information exists on the contribution of cholinergic receptors to this process. Here we evaluate for the first time the proposition that, as in mammals, muscarinic ACh receptors (mAChRs) contribute to memory formation in Drosophila. Our results show that pharmacological and genetic blockade of mAChRs in MB disrupts olfactory aversive memory in larvae. This effect is not explained by an alteration in the ability of animals to respond to odorants or to execute motor programs. These results show that mAChRs in MB contribute to generating olfactory memories in Drosophila.http://dx.doi.org/10.1155/2015/658918
spellingShingle Bryon Silva
Claudia Molina-Fernández
María Beatriz Ugalde
Eduardo I. Tognarelli
Cristian Angel
Jorge M. Campusano
Muscarinic ACh Receptors Contribute to Aversive Olfactory Learning in Drosophila
Neural Plasticity
title Muscarinic ACh Receptors Contribute to Aversive Olfactory Learning in Drosophila
title_full Muscarinic ACh Receptors Contribute to Aversive Olfactory Learning in Drosophila
title_fullStr Muscarinic ACh Receptors Contribute to Aversive Olfactory Learning in Drosophila
title_full_unstemmed Muscarinic ACh Receptors Contribute to Aversive Olfactory Learning in Drosophila
title_short Muscarinic ACh Receptors Contribute to Aversive Olfactory Learning in Drosophila
title_sort muscarinic ach receptors contribute to aversive olfactory learning in drosophila
url http://dx.doi.org/10.1155/2015/658918
work_keys_str_mv AT bryonsilva muscarinicachreceptorscontributetoaversiveolfactorylearningindrosophila
AT claudiamolinafernandez muscarinicachreceptorscontributetoaversiveolfactorylearningindrosophila
AT mariabeatrizugalde muscarinicachreceptorscontributetoaversiveolfactorylearningindrosophila
AT eduardoitognarelli muscarinicachreceptorscontributetoaversiveolfactorylearningindrosophila
AT cristianangel muscarinicachreceptorscontributetoaversiveolfactorylearningindrosophila
AT jorgemcampusano muscarinicachreceptorscontributetoaversiveolfactorylearningindrosophila