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GABA transporters (gamma-aminobutyric acid transporters) are a family of neurotransmitter / sodium symporters, belonging to the solute carrier 6 family. [1] [2] They are found in various regions of the brain in different cell types, such as neurons and astrocytes.
The GABA receptors are a class of receptors that respond to the neurotransmitter gamma-aminobutyric acid (GABA), the chief inhibitory compound in the mature vertebrate central nervous system. There are two classes of GABA receptors: GABA A and GABA B .
The GABA A-rho receptor (previously known as the GABA C receptor) is a subclass of GABA A receptors composed entirely of rho (ρ) subunits. GABA A receptors including those of the ρ-subclass are ligand-gated ion channels responsible for mediating the effects of gamma-amino butyric acid (), the major inhibitory neurotransmitter in the brain.
The ionotropic GABA A receptor protein complex is also the molecular target of the benzodiazepine class of tranquilizer drugs. Benzodiazepines do not bind to the same receptor site on the protein complex as does the endogenous ligand GABA (whose binding site is located between α- and β-subunits), but bind to distinct benzodiazepine binding sites situated at the interface between the α- and ...
The only difference noted so far is a slight elevation of brain Taurine levels. [2] This was an unexpected finding, but is in agreement with the notion that GAT2 permits efflux of GABA and taurine from the brain to circulating blood through the blood brain barrier. [3]
Otherwise known as gamma-aminobutyric acid, GABA is an amino acid produced in the brain. Here, experts explain GABA uses and side effects. Everything You Need to Know About GABA, an Essential ...
In the mammalian brain, two predominant, differentially expressed isoforms of the GABA B1 are transcribed from the Gabbr1 gene, GABA B(1a) and GABA B(1b), which are conserved in different species including humans. [12] This might potentially offer more complexity in terms of the function due to different composition of the receptor. [12]
GABA is the major inhibitory neurotransmitter in the mammalian brain where it acts at GABA A receptors, which are ligand-gated chloride channels. Chloride conductance of these channels can be modulated by agents such as benzodiazepines that bind to the GABA A receptor. At least 16 distinct subunits of GABA A receptors have been