Acute modulation of calcium currents and synaptic transmission by gabapentinoids

Gabapentin and pregabalin are anticonvulsant drugs that are extensively used for the treatment of several neurological and psychiatric disorders. Gabapentinoids (GBPs) are known to have a high affinity binding to α2δ-1 and α2δ-2 auxiliary subunit of specific voltage-gated calcium channels. Despite t...

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Autores principales: Uchitel, O.D., Di Guilmi, M.N., Urbano, F.J., Inchauspe, C.G.
Formato: JOUR
Materias:
Mus
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_19336950_v4_n6_p_Uchitel
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spelling todo:paper_19336950_v4_n6_p_Uchitel2023-10-03T16:36:12Z Acute modulation of calcium currents and synaptic transmission by gabapentinoids Uchitel, O.D. Di Guilmi, M.N. Urbano, F.J. Inchauspe, C.G. Calcium channels Calyx of held Gabapentin Mice Neuromuscular junction Pregabalin Synaptic transmission 4 aminobutyric acid amino acid transporter calcium channel P type calcium channel Q type gabapentin glycine n methyl dextro aspartic acid neurotransmitter potassium channel pregabalin sodium channel thrombospondin voltage gated calcium channel 4 aminobutyric acid amine anticonvulsive agent calcium channel cyclohexanecarboxylic acid derivative drug derivative gabapentin ligand pregabalin binding affinity calcium current central nervous system dose response drug protein binding drug targeting electrophysiology human ligand binding modulation neurochemistry neuromuscular synapse neurotransmitter release nonhuman protein interaction review skeletal muscle spinal ganglion synaptic transmission animal binding competition binding site brain calcium signaling drug effect kinetics metabolism synapse synaptic potential synaptosome Mus Amines Animals Anticonvulsants Binding Sites Binding, Competitive Brain Calcium Channels Calcium Signaling Cyclohexanecarboxylic Acids Dose-Response Relationship, Drug gamma-Aminobutyric Acid Humans Kinetics Ligands Presynaptic Terminals Synapses Synaptic Potentials Synaptic Transmission Gabapentin and pregabalin are anticonvulsant drugs that are extensively used for the treatment of several neurological and psychiatric disorders. Gabapentinoids (GBPs) are known to have a high affinity binding to α2δ-1 and α2δ-2 auxiliary subunit of specific voltage-gated calcium channels. Despite the confusing effects reported on Ca2+ currents, most of the studies showed that GBPs reduced release of various neurotransmitters from synapses in several neuronal tissues. We showed that acute in vitro application of pregabalin could reduce in a dose dependent manner synaptic transmission in both neuromuscular junctions and calyx of Held-MNTB excitatory synapses. Furthermore presynaptic Ca 2+ currents treated with pregabalin are reduced in amplitude, do not show inactivation at a clinically relevant low concentration of 100 μM and activate and deactive faster. These results suggest novel modulatory role of acute pregabalin that might contribute to better understanding its anticonvulsant/analgesic clinical effects. © 2010 Landes Bioscience. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_19336950_v4_n6_p_Uchitel
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Calcium channels
Calyx of held
Gabapentin
Mice
Neuromuscular junction
Pregabalin
Synaptic transmission
4 aminobutyric acid
amino acid transporter
calcium channel P type
calcium channel Q type
gabapentin
glycine
n methyl dextro aspartic acid
neurotransmitter
potassium channel
pregabalin
sodium channel
thrombospondin
voltage gated calcium channel
4 aminobutyric acid
amine
anticonvulsive agent
calcium channel
cyclohexanecarboxylic acid derivative
drug derivative
gabapentin
ligand
pregabalin
binding affinity
calcium current
central nervous system
dose response
drug protein binding
drug targeting
electrophysiology
human
ligand binding
modulation
neurochemistry
neuromuscular synapse
neurotransmitter release
nonhuman
protein interaction
review
skeletal muscle
spinal ganglion
synaptic transmission
animal
binding competition
binding site
brain
calcium signaling
drug effect
kinetics
metabolism
synapse
synaptic potential
synaptosome
Mus
Amines
Animals
Anticonvulsants
Binding Sites
Binding, Competitive
Brain
Calcium Channels
Calcium Signaling
Cyclohexanecarboxylic Acids
Dose-Response Relationship, Drug
gamma-Aminobutyric Acid
Humans
Kinetics
Ligands
Presynaptic Terminals
Synapses
Synaptic Potentials
Synaptic Transmission
spellingShingle Calcium channels
Calyx of held
Gabapentin
Mice
Neuromuscular junction
Pregabalin
Synaptic transmission
4 aminobutyric acid
amino acid transporter
calcium channel P type
calcium channel Q type
gabapentin
glycine
n methyl dextro aspartic acid
neurotransmitter
potassium channel
pregabalin
sodium channel
thrombospondin
voltage gated calcium channel
4 aminobutyric acid
amine
anticonvulsive agent
calcium channel
cyclohexanecarboxylic acid derivative
drug derivative
gabapentin
ligand
pregabalin
binding affinity
calcium current
central nervous system
dose response
drug protein binding
drug targeting
electrophysiology
human
ligand binding
modulation
neurochemistry
neuromuscular synapse
neurotransmitter release
nonhuman
protein interaction
review
skeletal muscle
spinal ganglion
synaptic transmission
animal
binding competition
binding site
brain
calcium signaling
drug effect
kinetics
metabolism
synapse
synaptic potential
synaptosome
Mus
Amines
Animals
Anticonvulsants
Binding Sites
Binding, Competitive
Brain
Calcium Channels
Calcium Signaling
Cyclohexanecarboxylic Acids
Dose-Response Relationship, Drug
gamma-Aminobutyric Acid
Humans
Kinetics
Ligands
Presynaptic Terminals
Synapses
Synaptic Potentials
Synaptic Transmission
Uchitel, O.D.
Di Guilmi, M.N.
Urbano, F.J.
Inchauspe, C.G.
Acute modulation of calcium currents and synaptic transmission by gabapentinoids
topic_facet Calcium channels
Calyx of held
Gabapentin
Mice
Neuromuscular junction
Pregabalin
Synaptic transmission
4 aminobutyric acid
amino acid transporter
calcium channel P type
calcium channel Q type
gabapentin
glycine
n methyl dextro aspartic acid
neurotransmitter
potassium channel
pregabalin
sodium channel
thrombospondin
voltage gated calcium channel
4 aminobutyric acid
amine
anticonvulsive agent
calcium channel
cyclohexanecarboxylic acid derivative
drug derivative
gabapentin
ligand
pregabalin
binding affinity
calcium current
central nervous system
dose response
drug protein binding
drug targeting
electrophysiology
human
ligand binding
modulation
neurochemistry
neuromuscular synapse
neurotransmitter release
nonhuman
protein interaction
review
skeletal muscle
spinal ganglion
synaptic transmission
animal
binding competition
binding site
brain
calcium signaling
drug effect
kinetics
metabolism
synapse
synaptic potential
synaptosome
Mus
Amines
Animals
Anticonvulsants
Binding Sites
Binding, Competitive
Brain
Calcium Channels
Calcium Signaling
Cyclohexanecarboxylic Acids
Dose-Response Relationship, Drug
gamma-Aminobutyric Acid
Humans
Kinetics
Ligands
Presynaptic Terminals
Synapses
Synaptic Potentials
Synaptic Transmission
description Gabapentin and pregabalin are anticonvulsant drugs that are extensively used for the treatment of several neurological and psychiatric disorders. Gabapentinoids (GBPs) are known to have a high affinity binding to α2δ-1 and α2δ-2 auxiliary subunit of specific voltage-gated calcium channels. Despite the confusing effects reported on Ca2+ currents, most of the studies showed that GBPs reduced release of various neurotransmitters from synapses in several neuronal tissues. We showed that acute in vitro application of pregabalin could reduce in a dose dependent manner synaptic transmission in both neuromuscular junctions and calyx of Held-MNTB excitatory synapses. Furthermore presynaptic Ca 2+ currents treated with pregabalin are reduced in amplitude, do not show inactivation at a clinically relevant low concentration of 100 μM and activate and deactive faster. These results suggest novel modulatory role of acute pregabalin that might contribute to better understanding its anticonvulsant/analgesic clinical effects. © 2010 Landes Bioscience.
format JOUR
author Uchitel, O.D.
Di Guilmi, M.N.
Urbano, F.J.
Inchauspe, C.G.
author_facet Uchitel, O.D.
Di Guilmi, M.N.
Urbano, F.J.
Inchauspe, C.G.
author_sort Uchitel, O.D.
title Acute modulation of calcium currents and synaptic transmission by gabapentinoids
title_short Acute modulation of calcium currents and synaptic transmission by gabapentinoids
title_full Acute modulation of calcium currents and synaptic transmission by gabapentinoids
title_fullStr Acute modulation of calcium currents and synaptic transmission by gabapentinoids
title_full_unstemmed Acute modulation of calcium currents and synaptic transmission by gabapentinoids
title_sort acute modulation of calcium currents and synaptic transmission by gabapentinoids
url http://hdl.handle.net/20.500.12110/paper_19336950_v4_n6_p_Uchitel
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