Cargando…

Increase in cyclic AMP concentration in a cerebral giant interneuron mimics part of a memory trace for conditioned taste aversion of the pond snail

Conditioned taste aversion (CTA) can be classically conditioned in the pond snail Lymnaea stagnalis and subsequently be consolidated into long-term memory (LTM). The neural trace that subserves CTA-LTM can be summarized as follows: A polysynaptic inhibitory postsynaptic potential recorded in the neu...

Descripción completa

Detalles Bibliográficos
Autores principales: Otsuka, Emi, Matsunaga, Miho, Okada, Ryuichi, Yamagishi, Miki, Okuta, Akiko, Lukowiak, Ken, Ito, Etsuro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Biophysical Society of Japan (BSJ) 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4629678/
https://www.ncbi.nlm.nih.gov/pubmed/27493554
http://dx.doi.org/10.2142/biophysics.9.161
_version_ 1782398611829555200
author Otsuka, Emi
Matsunaga, Miho
Okada, Ryuichi
Yamagishi, Miki
Okuta, Akiko
Lukowiak, Ken
Ito, Etsuro
author_facet Otsuka, Emi
Matsunaga, Miho
Okada, Ryuichi
Yamagishi, Miki
Okuta, Akiko
Lukowiak, Ken
Ito, Etsuro
author_sort Otsuka, Emi
collection PubMed
description Conditioned taste aversion (CTA) can be classically conditioned in the pond snail Lymnaea stagnalis and subsequently be consolidated into long-term memory (LTM). The neural trace that subserves CTA-LTM can be summarized as follows: A polysynaptic inhibitory postsynaptic potential recorded in the neuron 1 medial (N1M) cell in the conditioned snails as a result of activation of the cerebral giant cell (CGC) is larger and lasts longer than that in control snails. The N1M cell is ultimately activated by the CGC via the neuron 3 tonic (N3t) cell. That is, the inhibitory monosynaptic inputs from the N3t cell to the N1M cell are facilitated. The N1M and N3t cells are the members of feeding central pattern generator, whereas the CGC is a multimodal interneuron thought to play a key role in feeding behavior. Here we examined the involvement of a second messenger, cAMP, in the establishment of the memory trace. We injected cAMP into the CGC and monitored the potentials of the B3 motor neuron activated by the CGC. B3 activity is used as an index for the synaptic inputs from the N3t cell to the N1M cell. We found that the B3 potentials were transiently enlarged. Thus, when the cAMP concentration is increased in the CGC by taste aversion training, cAMP-induced changes may play a key role in the establishment of a memory trace in the N3t cell.
format Online
Article
Text
id pubmed-4629678
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher The Biophysical Society of Japan (BSJ)
record_format MEDLINE/PubMed
spelling pubmed-46296782016-08-04 Increase in cyclic AMP concentration in a cerebral giant interneuron mimics part of a memory trace for conditioned taste aversion of the pond snail Otsuka, Emi Matsunaga, Miho Okada, Ryuichi Yamagishi, Miki Okuta, Akiko Lukowiak, Ken Ito, Etsuro Biophysics (Nagoya-shi) Regular Article Conditioned taste aversion (CTA) can be classically conditioned in the pond snail Lymnaea stagnalis and subsequently be consolidated into long-term memory (LTM). The neural trace that subserves CTA-LTM can be summarized as follows: A polysynaptic inhibitory postsynaptic potential recorded in the neuron 1 medial (N1M) cell in the conditioned snails as a result of activation of the cerebral giant cell (CGC) is larger and lasts longer than that in control snails. The N1M cell is ultimately activated by the CGC via the neuron 3 tonic (N3t) cell. That is, the inhibitory monosynaptic inputs from the N3t cell to the N1M cell are facilitated. The N1M and N3t cells are the members of feeding central pattern generator, whereas the CGC is a multimodal interneuron thought to play a key role in feeding behavior. Here we examined the involvement of a second messenger, cAMP, in the establishment of the memory trace. We injected cAMP into the CGC and monitored the potentials of the B3 motor neuron activated by the CGC. B3 activity is used as an index for the synaptic inputs from the N3t cell to the N1M cell. We found that the B3 potentials were transiently enlarged. Thus, when the cAMP concentration is increased in the CGC by taste aversion training, cAMP-induced changes may play a key role in the establishment of a memory trace in the N3t cell. The Biophysical Society of Japan (BSJ) 2013-11-13 /pmc/articles/PMC4629678/ /pubmed/27493554 http://dx.doi.org/10.2142/biophysics.9.161 Text en ©2013 THE BIOPHYSICAL SOCIETY OF JAPAN
spellingShingle Regular Article
Otsuka, Emi
Matsunaga, Miho
Okada, Ryuichi
Yamagishi, Miki
Okuta, Akiko
Lukowiak, Ken
Ito, Etsuro
Increase in cyclic AMP concentration in a cerebral giant interneuron mimics part of a memory trace for conditioned taste aversion of the pond snail
title Increase in cyclic AMP concentration in a cerebral giant interneuron mimics part of a memory trace for conditioned taste aversion of the pond snail
title_full Increase in cyclic AMP concentration in a cerebral giant interneuron mimics part of a memory trace for conditioned taste aversion of the pond snail
title_fullStr Increase in cyclic AMP concentration in a cerebral giant interneuron mimics part of a memory trace for conditioned taste aversion of the pond snail
title_full_unstemmed Increase in cyclic AMP concentration in a cerebral giant interneuron mimics part of a memory trace for conditioned taste aversion of the pond snail
title_short Increase in cyclic AMP concentration in a cerebral giant interneuron mimics part of a memory trace for conditioned taste aversion of the pond snail
title_sort increase in cyclic amp concentration in a cerebral giant interneuron mimics part of a memory trace for conditioned taste aversion of the pond snail
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4629678/
https://www.ncbi.nlm.nih.gov/pubmed/27493554
http://dx.doi.org/10.2142/biophysics.9.161
work_keys_str_mv AT otsukaemi increaseincyclicampconcentrationinacerebralgiantinterneuronmimicspartofamemorytraceforconditionedtasteaversionofthepondsnail
AT matsunagamiho increaseincyclicampconcentrationinacerebralgiantinterneuronmimicspartofamemorytraceforconditionedtasteaversionofthepondsnail
AT okadaryuichi increaseincyclicampconcentrationinacerebralgiantinterneuronmimicspartofamemorytraceforconditionedtasteaversionofthepondsnail
AT yamagishimiki increaseincyclicampconcentrationinacerebralgiantinterneuronmimicspartofamemorytraceforconditionedtasteaversionofthepondsnail
AT okutaakiko increaseincyclicampconcentrationinacerebralgiantinterneuronmimicspartofamemorytraceforconditionedtasteaversionofthepondsnail
AT lukowiakken increaseincyclicampconcentrationinacerebralgiantinterneuronmimicspartofamemorytraceforconditionedtasteaversionofthepondsnail
AT itoetsuro increaseincyclicampconcentrationinacerebralgiantinterneuronmimicspartofamemorytraceforconditionedtasteaversionofthepondsnail