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Synaptic inhibition and γ-aminobutyric acid in the mammalian central nervous system

Signal transmission through synapses connecting two neurons is mediated by release of neurotransmitter from the presynaptic axon terminals and activation of its receptor at the postsynaptic neurons. γ-Aminobutyric acid (GABA), non-protein amino acid formed by decarboxylation of glutamic acid, is a p...

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Autor principal: OBATA, Kunihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japan Academy 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3669732/
https://www.ncbi.nlm.nih.gov/pubmed/23574805
http://dx.doi.org/10.2183/pjab.89.139
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author OBATA, Kunihiko
author_facet OBATA, Kunihiko
author_sort OBATA, Kunihiko
collection PubMed
description Signal transmission through synapses connecting two neurons is mediated by release of neurotransmitter from the presynaptic axon terminals and activation of its receptor at the postsynaptic neurons. γ-Aminobutyric acid (GABA), non-protein amino acid formed by decarboxylation of glutamic acid, is a principal neurotransmitter at inhibitory synapses of vertebrate and invertebrate nervous system. On one hand glutamic acid serves as a principal excitatory neurotransmitter. This article reviews GABA researches on; (1) synaptic inhibition by membrane hyperpolarization, (2) exclusive localization in inhibitory neurons, (3) release from inhibitory neurons, (4) excitatory action at developmental stage, (5) phenotype of GABA-deficient mouse produced by gene-targeting, (6) developmental adjustment of neural network and (7) neurological/psychiatric disorder. In the end, GABA functions in simple nervous system and plants, and non-amino acid neurotransmitters were supplemented.
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spelling pubmed-36697322013-07-17 Synaptic inhibition and γ-aminobutyric acid in the mammalian central nervous system OBATA, Kunihiko Proc Jpn Acad Ser B Phys Biol Sci Review Signal transmission through synapses connecting two neurons is mediated by release of neurotransmitter from the presynaptic axon terminals and activation of its receptor at the postsynaptic neurons. γ-Aminobutyric acid (GABA), non-protein amino acid formed by decarboxylation of glutamic acid, is a principal neurotransmitter at inhibitory synapses of vertebrate and invertebrate nervous system. On one hand glutamic acid serves as a principal excitatory neurotransmitter. This article reviews GABA researches on; (1) synaptic inhibition by membrane hyperpolarization, (2) exclusive localization in inhibitory neurons, (3) release from inhibitory neurons, (4) excitatory action at developmental stage, (5) phenotype of GABA-deficient mouse produced by gene-targeting, (6) developmental adjustment of neural network and (7) neurological/psychiatric disorder. In the end, GABA functions in simple nervous system and plants, and non-amino acid neurotransmitters were supplemented. The Japan Academy 2013-04-11 /pmc/articles/PMC3669732/ /pubmed/23574805 http://dx.doi.org/10.2183/pjab.89.139 Text en © 2013 The Japan Academy This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
OBATA, Kunihiko
Synaptic inhibition and γ-aminobutyric acid in the mammalian central nervous system
title Synaptic inhibition and γ-aminobutyric acid in the mammalian central nervous system
title_full Synaptic inhibition and γ-aminobutyric acid in the mammalian central nervous system
title_fullStr Synaptic inhibition and γ-aminobutyric acid in the mammalian central nervous system
title_full_unstemmed Synaptic inhibition and γ-aminobutyric acid in the mammalian central nervous system
title_short Synaptic inhibition and γ-aminobutyric acid in the mammalian central nervous system
title_sort synaptic inhibition and γ-aminobutyric acid in the mammalian central nervous system
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3669732/
https://www.ncbi.nlm.nih.gov/pubmed/23574805
http://dx.doi.org/10.2183/pjab.89.139
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