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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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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. |
format | Online Article Text |
id | pubmed-4655456 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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