Selective Recruitment of Presynaptic and Postsynaptic Forms of mGluR-LTD.

CA1 DHPG hippocampus long-term depression (LTD) metabotropic glutamate (mGlu) receptor

Journal

Frontiers in synaptic neuroscience
ISSN: 1663-3563
Titre abrégé: Front Synaptic Neurosci
Pays: Switzerland
ID NLM: 101548972

Informations de publication

Date de publication:
2022
Historique:
received: 18 01 2022
accepted: 20 04 2022
entrez: 26 5 2022
pubmed: 27 5 2022
medline: 27 5 2022
Statut: epublish

Résumé

In area CA1 of the hippocampus, long-term depression (LTD) can be induced by activating group I metabotropic glutamate receptors (mGluRs), with the selective agonist DHPG. There is evidence that mGluR-LTD can be expressed by either a decrease in the probability of neurotransmitter release [P(r)] or by a change in postsynaptic AMPA receptor number. However, what determines the locus of expression is unknown. We investigated the expression mechanisms of mGluR-LTD using either a low (30 μM) or a high (100 μM) concentration of (RS)-DHPG. We found that 30 μM DHPG generated presynaptic LTD that required the co-activation of NMDA receptors, whereas 100 μM DHPG resulted in postsynaptic LTD that was independent of the activation of NMDA receptors. We found that both forms of LTD occur at the same synapses and that these may constitute the population with the lowest basal P(r). Our results reveal an unexpected complexity to mGluR-mediated synaptic plasticity in the hippocampus.

Identifiants

pubmed: 35615440
doi: 10.3389/fnsyn.2022.857675
pmc: PMC9126322
doi:

Types de publication

Journal Article

Langues

eng

Pagination

857675

Informations de copyright

Copyright © 2022 Sanderson, Ralph, Amici, Ng, Kaang, Zhuo, Kim, Georgiou and Collingridge.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Thomas M Sanderson (TM)

Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Sinai Health System, Toronto, ON, Canada.
Department of Brain and Cognitive Sciences, College of Natural Sciences, Seoul National University, Seoul, South Korea.
Neuroscience Research Institute, Seoul National University College of Medicine, Seoul, South Korea.
School of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol, United Kingdom.

Liam T Ralph (LT)

Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Sinai Health System, Toronto, ON, Canada.
Department of Physiology, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada.

Mascia Amici (M)

School of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol, United Kingdom.

Ai Na Ng (AN)

School of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol, United Kingdom.

Bong-Kiun Kaang (BK)

Department of Brain and Cognitive Sciences, College of Natural Sciences, Seoul National University, Seoul, South Korea.
Department of Biological Sciences, College of Natural Sciences, Seoul National University, Seoul, South Korea.

Min Zhuo (M)

Department of Brain and Cognitive Sciences, College of Natural Sciences, Seoul National University, Seoul, South Korea.
Department of Physiology, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada.

Sang Jeong Kim (SJ)

Department of Brain and Cognitive Sciences, College of Natural Sciences, Seoul National University, Seoul, South Korea.
Neuroscience Research Institute, Seoul National University College of Medicine, Seoul, South Korea.

John Georgiou (J)

Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Sinai Health System, Toronto, ON, Canada.

Graham L Collingridge (GL)

Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Sinai Health System, Toronto, ON, Canada.
Department of Brain and Cognitive Sciences, College of Natural Sciences, Seoul National University, Seoul, South Korea.
School of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol, United Kingdom.
Department of Physiology, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada.
Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, ON, Canada.

Classifications MeSH