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PMID: 7903116 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Role of a metabotropic glutamate receptor in synaptic modulation in the accessory olfactory bulb.

Nature ·Vol. 366 ·No. 6456 ·1993-12-16 ·Pages 687-90

Hayashi Y, Momiyama A, Takahashi T, Ohishi H, Ogawa-Meguro R, Shigemoto R, Mizuno N, Nakanishi S

Abstract

Various functions of glutamate transmission are mediated by both ionotropic and metabotropic glutamate receptors. The metabotropic glutamate receptors (mGluRs) consists of at least six different subtypes that are classified into three subgroups, mGluR1/mGluR5, mGluR2/mGluR3, and mGluR4/mGluR6 (refs 1-5), but their physiological roles are largely unknown. Here we report the identification of a very potent agonist for mGluR2/mGluR3, DCG-IV, and the specific localization of mGluR2 in granule cell dendrites that form dendrodendritic synapses with mitral cells in the accessory olfactory bulb. Using the DCG-IV agonist for mGluR2 in combination with slice patch-recording, we demonstrate that the granule cell mGluR2 presynaptically suppresses inhibitory GABA (gamma-aminobutyrate) transmission to the mitral cell. Our results indicate that mGluR2 in granule cells plays an important role in the persistent excitation of olfactory sensory transmission in the accessory olfactory bulb by relieving mitral cells from the GABA inhibition.

MeSH Terms
Animals CHO Cells Cricetinae Cyclopropanes/pharmacology Dendrites/physiology Glutamates/metabolism Glutamic Acid Glycine/analogs & derivatives,pharmacology In Vitro Techniques Interneurons/physiology Olfactory Bulb/cytology,physiology Rats Receptors, Glutamate/drug effects,physiology Receptors, N-Methyl-D-Aspartate/drug effects Synaptic Transmission/drug effects,physiology gamma-Aminobutyric Acid/metabolism,physiology
Chemicals
Cyclopropanes Glutamates Receptors, Glutamate Receptors, N-Methyl-D-Aspartate 2-(2,3-dicarboxycyclopropyl)glycine Glutamic Acid gamma-Aminobutyric Acid Glycine
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Hayashi Y
Department of Pharmacology, Kyoto University Faculty of Medicine, Japan.
Momiyama A
Takahashi T
Ohishi H
Ogawa-Meguro R
Shigemoto R
Mizuno N
Nakanishi S
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
1993-12-16
Pages
687-90
Language
English
Region
England
NLM ID
0410462
Subset
IM
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