Cargando…

Altered Short-Term Synaptic Plasticity in Mice Lacking the Metabotropic Glutamate Receptor mGlu7

Eight subtypes of metabotropic glutamate (mGlu) receptors have been identified of which two, mGlu5 and mGlu7, are highly expressed at synapses made between CA3 and CA1 pyramidal neurons in the hippocampus. This input, the Schaffer collateral-commissural pathway, displays robust long-term potentiatio...

Descripción completa

Detalles Bibliográficos
Autores principales: Bushell, Trevor J., Sansig, Gilles, Collett, Valerie J., van der Putten, Herman, Collingridge, Graham L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: TheScientificWorldJOURNAL 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6009301/
https://www.ncbi.nlm.nih.gov/pubmed/12805997
http://dx.doi.org/10.1100/tsw.2002.146
_version_ 1783333351565819904
author Bushell, Trevor J.
Sansig, Gilles
Collett, Valerie J.
van der Putten, Herman
Collingridge, Graham L.
author_facet Bushell, Trevor J.
Sansig, Gilles
Collett, Valerie J.
van der Putten, Herman
Collingridge, Graham L.
author_sort Bushell, Trevor J.
collection PubMed
description Eight subtypes of metabotropic glutamate (mGlu) receptors have been identified of which two, mGlu5 and mGlu7, are highly expressed at synapses made between CA3 and CA1 pyramidal neurons in the hippocampus. This input, the Schaffer collateral-commissural pathway, displays robust long-term potentiation (LTP), a process believed to utilise molecular mechanisms that are key processes involved in the synaptic basis of learning and memory. To investigate the possible function in LTP of mGlu7 receptors, a subtype for which no specific antagonists exist, we generated a mouse lacking this receptor, by homologous recombination. We found that LTP could be induced in mGlu7-/- mice and that once the potentiation had reached a stable level there was no difference in the magnitude of LTP between mGlu7-/- mice and their littermate controls. However, the initial decremental phase of LTP, known as short-term potentiation (STP), was greatly attenuated in the mGlu7-/- mouse. In addition, there was less frequency facilitation during, and less post-tetanic potentiation following, a high frequency train in the mGlu7-/- mouse. These results show that the absence of mGlu7 receptors results in alterations in short-term synaptic plasticity in the hippocampus.
format Online
Article
Text
id pubmed-6009301
institution National Center for Biotechnology Information
language English
publishDate 2002
publisher TheScientificWorldJOURNAL
record_format MEDLINE/PubMed
spelling pubmed-60093012018-07-04 Altered Short-Term Synaptic Plasticity in Mice Lacking the Metabotropic Glutamate Receptor mGlu7 Bushell, Trevor J. Sansig, Gilles Collett, Valerie J. van der Putten, Herman Collingridge, Graham L. ScientificWorldJournal Short Communication Eight subtypes of metabotropic glutamate (mGlu) receptors have been identified of which two, mGlu5 and mGlu7, are highly expressed at synapses made between CA3 and CA1 pyramidal neurons in the hippocampus. This input, the Schaffer collateral-commissural pathway, displays robust long-term potentiation (LTP), a process believed to utilise molecular mechanisms that are key processes involved in the synaptic basis of learning and memory. To investigate the possible function in LTP of mGlu7 receptors, a subtype for which no specific antagonists exist, we generated a mouse lacking this receptor, by homologous recombination. We found that LTP could be induced in mGlu7-/- mice and that once the potentiation had reached a stable level there was no difference in the magnitude of LTP between mGlu7-/- mice and their littermate controls. However, the initial decremental phase of LTP, known as short-term potentiation (STP), was greatly attenuated in the mGlu7-/- mouse. In addition, there was less frequency facilitation during, and less post-tetanic potentiation following, a high frequency train in the mGlu7-/- mouse. These results show that the absence of mGlu7 receptors results in alterations in short-term synaptic plasticity in the hippocampus. TheScientificWorldJOURNAL 2002-03-15 /pmc/articles/PMC6009301/ /pubmed/12805997 http://dx.doi.org/10.1100/tsw.2002.146 Text en Copyright © 2002 Trevor J. Bushell et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Bushell, Trevor J.
Sansig, Gilles
Collett, Valerie J.
van der Putten, Herman
Collingridge, Graham L.
Altered Short-Term Synaptic Plasticity in Mice Lacking the Metabotropic Glutamate Receptor mGlu7
title Altered Short-Term Synaptic Plasticity in Mice Lacking the Metabotropic Glutamate Receptor mGlu7
title_full Altered Short-Term Synaptic Plasticity in Mice Lacking the Metabotropic Glutamate Receptor mGlu7
title_fullStr Altered Short-Term Synaptic Plasticity in Mice Lacking the Metabotropic Glutamate Receptor mGlu7
title_full_unstemmed Altered Short-Term Synaptic Plasticity in Mice Lacking the Metabotropic Glutamate Receptor mGlu7
title_short Altered Short-Term Synaptic Plasticity in Mice Lacking the Metabotropic Glutamate Receptor mGlu7
title_sort altered short-term synaptic plasticity in mice lacking the metabotropic glutamate receptor mglu7
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6009301/
https://www.ncbi.nlm.nih.gov/pubmed/12805997
http://dx.doi.org/10.1100/tsw.2002.146
work_keys_str_mv AT bushelltrevorj alteredshorttermsynapticplasticityinmicelackingthemetabotropicglutamatereceptormglu7
AT sansiggilles alteredshorttermsynapticplasticityinmicelackingthemetabotropicglutamatereceptormglu7
AT collettvaleriej alteredshorttermsynapticplasticityinmicelackingthemetabotropicglutamatereceptormglu7
AT vanderputtenherman alteredshorttermsynapticplasticityinmicelackingthemetabotropicglutamatereceptormglu7
AT collingridgegrahaml alteredshorttermsynapticplasticityinmicelackingthemetabotropicglutamatereceptormglu7