Cargando…
Reinstatement of long-term memory following erasure of its behavioral and synaptic expression in Aplysia
Long-term memory (LTM) is believed to be stored in the brain as changes in synaptic connections. Here, we show that LTM storage and synaptic change can be dissociated. Cocultures of Aplysia sensory and motor neurons were trained with spaced pulses of serotonin, which induces long-term facilitation....
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4270066/ https://www.ncbi.nlm.nih.gov/pubmed/25402831 http://dx.doi.org/10.7554/eLife.03896 |
_version_ | 1782349439691653120 |
---|---|
author | Chen, Shanping Cai, Diancai Pearce, Kaycey Sun, Philip Y-W Roberts, Adam C Glanzman, David L |
author_facet | Chen, Shanping Cai, Diancai Pearce, Kaycey Sun, Philip Y-W Roberts, Adam C Glanzman, David L |
author_sort | Chen, Shanping |
collection | PubMed |
description | Long-term memory (LTM) is believed to be stored in the brain as changes in synaptic connections. Here, we show that LTM storage and synaptic change can be dissociated. Cocultures of Aplysia sensory and motor neurons were trained with spaced pulses of serotonin, which induces long-term facilitation. Serotonin (5HT) triggered growth of new presynaptic varicosities, a synaptic mechanism of long-term sensitization. Following 5HT training, two antimnemonic treatments—reconsolidation blockade and inhibition of PKM—caused the number of presynaptic varicosities to revert to the original, pretraining value. Surprisingly, the final synaptic structure was not achieved by targeted retraction of the 5HT-induced varicosities but, rather, by an apparently arbitrary retraction of both 5HT-induced and original synapses. In addition, we find evidence that the LTM for sensitization persists covertly after its apparent elimination by the same antimnemonic treatments that erase learning-related synaptic growth. These results challenge the idea that stable synapses store long-term memories. DOI: http://dx.doi.org/10.7554/eLife.03896.001 |
format | Online Article Text |
id | pubmed-4270066 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42700662015-01-29 Reinstatement of long-term memory following erasure of its behavioral and synaptic expression in Aplysia Chen, Shanping Cai, Diancai Pearce, Kaycey Sun, Philip Y-W Roberts, Adam C Glanzman, David L eLife Neuroscience Long-term memory (LTM) is believed to be stored in the brain as changes in synaptic connections. Here, we show that LTM storage and synaptic change can be dissociated. Cocultures of Aplysia sensory and motor neurons were trained with spaced pulses of serotonin, which induces long-term facilitation. Serotonin (5HT) triggered growth of new presynaptic varicosities, a synaptic mechanism of long-term sensitization. Following 5HT training, two antimnemonic treatments—reconsolidation blockade and inhibition of PKM—caused the number of presynaptic varicosities to revert to the original, pretraining value. Surprisingly, the final synaptic structure was not achieved by targeted retraction of the 5HT-induced varicosities but, rather, by an apparently arbitrary retraction of both 5HT-induced and original synapses. In addition, we find evidence that the LTM for sensitization persists covertly after its apparent elimination by the same antimnemonic treatments that erase learning-related synaptic growth. These results challenge the idea that stable synapses store long-term memories. DOI: http://dx.doi.org/10.7554/eLife.03896.001 eLife Sciences Publications, Ltd 2014-11-17 /pmc/articles/PMC4270066/ /pubmed/25402831 http://dx.doi.org/10.7554/eLife.03896 Text en Copyright © 2014, Chen et al 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 Chen, Shanping Cai, Diancai Pearce, Kaycey Sun, Philip Y-W Roberts, Adam C Glanzman, David L Reinstatement of long-term memory following erasure of its behavioral and synaptic expression in Aplysia |
title | Reinstatement of long-term memory following erasure of its behavioral and synaptic expression in Aplysia |
title_full | Reinstatement of long-term memory following erasure of its behavioral and synaptic expression in Aplysia |
title_fullStr | Reinstatement of long-term memory following erasure of its behavioral and synaptic expression in Aplysia |
title_full_unstemmed | Reinstatement of long-term memory following erasure of its behavioral and synaptic expression in Aplysia |
title_short | Reinstatement of long-term memory following erasure of its behavioral and synaptic expression in Aplysia |
title_sort | reinstatement of long-term memory following erasure of its behavioral and synaptic expression in aplysia |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4270066/ https://www.ncbi.nlm.nih.gov/pubmed/25402831 http://dx.doi.org/10.7554/eLife.03896 |
work_keys_str_mv | AT chenshanping reinstatementoflongtermmemoryfollowingerasureofitsbehavioralandsynapticexpressioninaplysia AT caidiancai reinstatementoflongtermmemoryfollowingerasureofitsbehavioralandsynapticexpressioninaplysia AT pearcekaycey reinstatementoflongtermmemoryfollowingerasureofitsbehavioralandsynapticexpressioninaplysia AT sunphilipyw reinstatementoflongtermmemoryfollowingerasureofitsbehavioralandsynapticexpressioninaplysia AT robertsadamc reinstatementoflongtermmemoryfollowingerasureofitsbehavioralandsynapticexpressioninaplysia AT glanzmandavidl reinstatementoflongtermmemoryfollowingerasureofitsbehavioralandsynapticexpressioninaplysia |