Results 321 to 330 of about 2,453,144 (355)
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GABA-receptors in peripheral tissues

Life Sciences, 1990
Gamma-aminobutyric acid (GABA) and its receptors are found in a wide range of peripheral tissues, including parts of the peripheral nervous system, endocrines, and non-neural tissues such as smooth muscle and the female reproductive system. In all these, both GABAA- and GABAB-receptor types are found, with good evidence for a physiological role in the ...
Jennifer Ong, David I.B. Kerr
openaire   +3 more sources

GABA(B) receptors are the first target of released GABA at lamina I inhibitory synapses in the adult rat spinal cord.

Journal of Neurophysiology, 2000
We have previously provided functional evidence that glycine and GABA are contained in the same synaptic vesicles and coreleased at the same synapses in lamina I of the rat spinal dorsal horn.
N. Chéry, Y. Koninck
semanticscholar   +1 more source

GABA(C) receptors as drug targets.

Current Drug Targets - CNS & Neurological Disorders, 2003
GABA(C) receptors are the least studied of the three major classes of GABA receptors. The physiological roles of GABA(C) receptors are still being unravelled and the pharmacology of these receptors is being developed. A range of agents has been described
G. Johnston   +3 more
semanticscholar   +1 more source

GABA Receptors and Phospholipids

1978
The sodium-independent binding of GABA to certain membrane preparations from rat brain exhibits many of the properties of the interaction of GABA with postsynaptic receptors anticipated from in vivo studies (see papers by Enna and Olsen, this meeting).
S. M. E. Kennedy, Graham A.R. Johnston
openaire   +2 more sources

GABA-B Receptors in Drosophila

2010
Drosophila melanogaster, the "fruit fly," is being increasingly used as an experimental model in neurosciences, including neuropharmacology. The advantages of Drosophila over typical mammalian models in neuropharmacology include better access to genetic manipulation and the availability of almost unlimited numbers of experimental subjects at relatively
Svetlana Dzitoyeva, Hari Manev
openaire   +3 more sources

Bicuculline and Central GABA Receptors

Nature, 1970
WE are unable to accept the implication by Krnjevic and his associates1 that we erred in reporting2 bicuculline to be a relatively specific antagonist of γ-aminobutyric acid (GABA) in the central nervous system of the cat.
David R. Curtis   +3 more
openaire   +3 more sources

Nonsynaptic Receptors for GABA and Glutamate

Current Topics in Medicinal Chemistry, 2006
The concept of nonsynaptic communication between neurons, once a heretic idea, has become a self-evident fact during the almost forty years since its original discovery. In this review we investigate whether the archetypical synaptic transmitters of the central nervous system, Glu and GABA, can operate via nonsynaptic transmission.
Arpad Mike, E.S. Vizi
openaire   +3 more sources

Presynaptic Ionotropic GABA Receptors

2007
Following the classical work on presynaptic inhibition in the spinal cord, recent work has revealed an astonishing abundance and diversity of presynaptic ionotropic GABA receptors. While modern techniques allow for detailed studies at the cellular and molecular level in almost all regions of the CNS, our understanding of the function of such receptors ...
Sergej Kolbaev   +2 more
openaire   +3 more sources

GABA and Its Receptors in Epilepsy

2004
Gamma-aminobutyric acid (GABA) is the principal inhibitory neurotransmitter in the mammalian brain. It acts through 2 classes of receptors, GABAA receptors that are ligand-operated ion channels and the G-protein-coupled metabotropic GABAB receptors. Impairment of GABAergic transmission by genetic mutations or application of GABA receptor antagonists ...
Susanne Pirker   +3 more
openaire   +3 more sources

Benzodiazepine interactions with GABA receptors

Neuroscience Letters, 1984
Benzodiazepines (BZs) produce most, if not all, of their pharmacological actions by specifically enhancing the effects of endogenous and exogenous GABA that are mediated by GABAA receptors. This potentiation consists in an increase of the apparent affinity of GABA for increasing chloride conductance without increase in its efficacy and, on the single ...
openaire   +3 more sources

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