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Spatial Object Recognition Enables Endogenous LTD that Curtails LTP in the Mouse Hippocampus

Although synaptic plasticity is believed to comprise the cellular substrate for learning and memory, limited direct evidence exists that hippocampus-dependent learning actually triggers synaptic plasticity. It is likely, however, that long-term potentiation (LTP) works in concert with its counterpar...

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Detalles Bibliográficos
Autores principales: Goh, Jinzhong Jeremy, Manahan-Vaughan, Denise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3615348/
https://www.ncbi.nlm.nih.gov/pubmed/22510536
http://dx.doi.org/10.1093/cercor/bhs089
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author Goh, Jinzhong Jeremy
Manahan-Vaughan, Denise
author_facet Goh, Jinzhong Jeremy
Manahan-Vaughan, Denise
author_sort Goh, Jinzhong Jeremy
collection PubMed
description Although synaptic plasticity is believed to comprise the cellular substrate for learning and memory, limited direct evidence exists that hippocampus-dependent learning actually triggers synaptic plasticity. It is likely, however, that long-term potentiation (LTP) works in concert with its counterpart, long-term depression (LTD) in the creation of spatial memory. It has been reported in rats that weak synaptic plasticity is facilitated into persistent plasticity if afferent stimulation is coupled with a novel spatial learning event. It is not known if this phenomenon also occurs in other species. We recorded from the hippocampal CA1 of freely behaving mice and observed that novel spatial learning triggers endogenous LTD. Specifically, we observed that LTD is enabled when test-pulse afferent stimulation is given during the learning of object constellations or during a spatial object recognition task. Intriguingly, LTP is significantly impaired by the same tasks, suggesting that LTD is the main cellular substrate for this type of learning. These data indicate that learning-facilitated plasticity is not exclusive to rats and that spatial learning leads to endogenous LTD in the hippocampus, suggesting an important role for this type of synaptic plasticity in the creation of hippocampus-dependent memory.
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spelling pubmed-36153482013-04-03 Spatial Object Recognition Enables Endogenous LTD that Curtails LTP in the Mouse Hippocampus Goh, Jinzhong Jeremy Manahan-Vaughan, Denise Cereb Cortex Articles Although synaptic plasticity is believed to comprise the cellular substrate for learning and memory, limited direct evidence exists that hippocampus-dependent learning actually triggers synaptic plasticity. It is likely, however, that long-term potentiation (LTP) works in concert with its counterpart, long-term depression (LTD) in the creation of spatial memory. It has been reported in rats that weak synaptic plasticity is facilitated into persistent plasticity if afferent stimulation is coupled with a novel spatial learning event. It is not known if this phenomenon also occurs in other species. We recorded from the hippocampal CA1 of freely behaving mice and observed that novel spatial learning triggers endogenous LTD. Specifically, we observed that LTD is enabled when test-pulse afferent stimulation is given during the learning of object constellations or during a spatial object recognition task. Intriguingly, LTP is significantly impaired by the same tasks, suggesting that LTD is the main cellular substrate for this type of learning. These data indicate that learning-facilitated plasticity is not exclusive to rats and that spatial learning leads to endogenous LTD in the hippocampus, suggesting an important role for this type of synaptic plasticity in the creation of hippocampus-dependent memory. Oxford University Press 2013-05 2012-04-17 /pmc/articles/PMC3615348/ /pubmed/22510536 http://dx.doi.org/10.1093/cercor/bhs089 Text en © The Authors 2012. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Goh, Jinzhong Jeremy
Manahan-Vaughan, Denise
Spatial Object Recognition Enables Endogenous LTD that Curtails LTP in the Mouse Hippocampus
title Spatial Object Recognition Enables Endogenous LTD that Curtails LTP in the Mouse Hippocampus
title_full Spatial Object Recognition Enables Endogenous LTD that Curtails LTP in the Mouse Hippocampus
title_fullStr Spatial Object Recognition Enables Endogenous LTD that Curtails LTP in the Mouse Hippocampus
title_full_unstemmed Spatial Object Recognition Enables Endogenous LTD that Curtails LTP in the Mouse Hippocampus
title_short Spatial Object Recognition Enables Endogenous LTD that Curtails LTP in the Mouse Hippocampus
title_sort spatial object recognition enables endogenous ltd that curtails ltp in the mouse hippocampus
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3615348/
https://www.ncbi.nlm.nih.gov/pubmed/22510536
http://dx.doi.org/10.1093/cercor/bhs089
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