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Toward elucidating diversity of neural mechanisms underlying insect learning

Insects are widely used as models to study neural mechanisms of learning and memory. Our recent studies on crickets, together with reports on other insect species, suggest that some fundamental differences exist in neural and molecular mechanisms of learning and memory among different species of ins...

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Autores principales: Mizunami, Makoto, Hamanaka, Yoshitaka, Nishino, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4655456/
https://www.ncbi.nlm.nih.gov/pubmed/26605053
http://dx.doi.org/10.1186/s40851-014-0008-6
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author Mizunami, Makoto
Hamanaka, Yoshitaka
Nishino, Hiroshi
author_facet Mizunami, Makoto
Hamanaka, Yoshitaka
Nishino, Hiroshi
author_sort Mizunami, Makoto
collection PubMed
description Insects are widely used as models to study neural mechanisms of learning and memory. Our recent studies on crickets, together with reports on other insect species, suggest that some fundamental differences exist in neural and molecular mechanisms of learning and memory among different species of insects, particularly between crickets and fruit flies. First, we suggested that in crickets octopamine (OA) and dopamine (DA) neurons convey reward and punishment signals, respectively, in associated learning. On the other hand, it has been reported that in fruit flies different sets of DA neurons convey reward or punishment signals. Secondly, we have suggested that in crickets OA and DA neurons participate in the retrieval of appetitive and aversive memories, respectively, while this is not the case in fruit flies. Thirdly, cyclic AMP signaling is critical for short-term memory formation in fruit flies, but not in crickets. Finally, nitric oxide-cyclic GMP signaling and calcium-calmodulin signaling are critical for long-term memory (LTM) formation in crickets, but such roles have not been reported in fruit flies. Not all of these differences can be ascribed to different experimental methods used in studies. We thus suggest that there are unexpected diversities in basic mechanisms of learning and memory among different insect species, especially between crickets and fruit flies. Studies on a larger number of insect species will help clarify the diversity of learning and memory mechanisms in relation to functional adaptation to the environment and evolutionary history.
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spelling pubmed-46554562015-11-24 Toward elucidating diversity of neural mechanisms underlying insect learning Mizunami, Makoto Hamanaka, Yoshitaka Nishino, Hiroshi Zoological Lett Review Insects are widely used as models to study neural mechanisms of learning and memory. Our recent studies on crickets, together with reports on other insect species, suggest that some fundamental differences exist in neural and molecular mechanisms of learning and memory among different species of insects, particularly between crickets and fruit flies. First, we suggested that in crickets octopamine (OA) and dopamine (DA) neurons convey reward and punishment signals, respectively, in associated learning. On the other hand, it has been reported that in fruit flies different sets of DA neurons convey reward or punishment signals. Secondly, we have suggested that in crickets OA and DA neurons participate in the retrieval of appetitive and aversive memories, respectively, while this is not the case in fruit flies. Thirdly, cyclic AMP signaling is critical for short-term memory formation in fruit flies, but not in crickets. Finally, nitric oxide-cyclic GMP signaling and calcium-calmodulin signaling are critical for long-term memory (LTM) formation in crickets, but such roles have not been reported in fruit flies. Not all of these differences can be ascribed to different experimental methods used in studies. We thus suggest that there are unexpected diversities in basic mechanisms of learning and memory among different insect species, especially between crickets and fruit flies. Studies on a larger number of insect species will help clarify the diversity of learning and memory mechanisms in relation to functional adaptation to the environment and evolutionary history. BioMed Central 2015-02-10 /pmc/articles/PMC4655456/ /pubmed/26605053 http://dx.doi.org/10.1186/s40851-014-0008-6 Text en © Mizunami et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Mizunami, Makoto
Hamanaka, Yoshitaka
Nishino, Hiroshi
Toward elucidating diversity of neural mechanisms underlying insect learning
title Toward elucidating diversity of neural mechanisms underlying insect learning
title_full Toward elucidating diversity of neural mechanisms underlying insect learning
title_fullStr Toward elucidating diversity of neural mechanisms underlying insect learning
title_full_unstemmed Toward elucidating diversity of neural mechanisms underlying insect learning
title_short Toward elucidating diversity of neural mechanisms underlying insect learning
title_sort toward elucidating diversity of neural mechanisms underlying insect learning
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4655456/
https://www.ncbi.nlm.nih.gov/pubmed/26605053
http://dx.doi.org/10.1186/s40851-014-0008-6
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