Quercetin antagonism of GABAAρ1 receptors is prevented by ascorbic acid through a redox-independent mechanism

Quercetin is a natural flavonoid widely distributed in plants that acts as a neuroprotective agent and modulates the activity of different synaptic receptors and ion channels, including the ionotropic GABA receptors. GABA Aρ1 receptors were shown to be antagonized by quercetin, but the mechanisms un...

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Autores principales: Calero, C.I., González, A.N.B., Gasulla, J., Alvarez, S., Evelson, P., Calvo, D.J.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00142999_v714_n1-3_p274_Calero
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spelling todo:paper_00142999_v714_n1-3_p274_Calero2023-10-03T14:12:11Z Quercetin antagonism of GABAAρ1 receptors is prevented by ascorbic acid through a redox-independent mechanism Calero, C.I. González, A.N.B. Gasulla, J. Alvarez, S. Evelson, P. Calvo, D.J. Allosteric modulator Ascorbic acid Flavonoid GABA receptor Quercetin 4 aminobutyric acid 4 aminobutyric acid A receptor 4 aminobutyric acid A receptor blocking agent 4 aminobutyric acid receptor ascorbic acid flavonoid histidine quercetin 4 aminobutyric acid A receptor 4 aminobutyric acid A receptor blocking agent ascorbic acid quercetin γ-aminobutyric acid Allosteric modulator allosterism animal article chemistry dose response drug antagonism drug effect human metabolism N-ethylmaleimide NEM antagonists and inhibitors drug effects γ-aminobutyric acid Allosteric modulator Ascorbic acid Flavonoid GABA GABA receptor N-ethylmaleimide NEM Quercetin Allosteric Regulation Animals Ascorbic Acid Dose-Response Relationship, Drug GABA-A Receptor Antagonists Histidine Humans Quercetin Receptors, GABA-A Allosteric Regulation Animals Ascorbic Acid Dose-Response Relationship, Drug GABA-A Receptor Antagonists Histidine Humans Quercetin Receptors, GABA-A Quercetin is a natural flavonoid widely distributed in plants that acts as a neuroprotective agent and modulates the activity of different synaptic receptors and ion channels, including the ionotropic GABA receptors. GABA Aρ1 receptors were shown to be antagonized by quercetin, but the mechanisms underlying these antagonistic actions are still unknown. We have analyzed here if the antagonistic action produced by quercetin on GABA Aρ1 receptors was related to its redox activity or due to alternative mechanism/s. Homomeric GABAAρ1 receptors were expressed in frog oocytes and GABA-evoked responses electro-physiologically recorded. Quercetin effects on GABAAρ1 receptors were examined in the absence or presence of ascorbic acid. Chemical protection of cysteines by selective sulfhydryl reagents and site directed mutagenesis experiments were also used to determine ρ1 subunit residues involved in quercetin actions. Quercetin antagonized GABAAρ1 receptor responses in a dose-dependent, fast and reversible manner. Quercetin inhibition was prevented in the presence of ascorbic acid, but not by thiol reagents that modify the extracellular Cys-loop of these receptors. H141, an aminoacidic residue located near to the ρ1 subunit GABA binding site, was involved in the allosteric modulation of GABAAρ1 receptors by several agents including ascorbic acid. Quercetin similarly antagonized GABA-evoked responses mediated by mutant H141DGABAAρ1 and wild-type receptors, but prevention exerted by ascorbic acid on quercetin effects was impaired in mutant receptors. Taken together the present results suggest that quercetin antagonistic actions on GABAAρ1 receptors are mediated through a redox-independent allosteric mechanism. © 2013 Elsevier B.V. All rights reserved. Fil:Calero, C.I. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Calvo, D.J. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00142999_v714_n1-3_p274_Calero
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Allosteric modulator
Ascorbic acid
Flavonoid
GABA receptor
Quercetin
4 aminobutyric acid
4 aminobutyric acid A receptor
4 aminobutyric acid A receptor blocking agent
4 aminobutyric acid receptor
ascorbic acid
flavonoid
histidine
quercetin
4 aminobutyric acid A receptor
4 aminobutyric acid A receptor blocking agent
ascorbic acid
quercetin
γ-aminobutyric acid
Allosteric modulator
allosterism
animal
article
chemistry
dose response
drug antagonism
drug effect
human
metabolism
N-ethylmaleimide
NEM
antagonists and inhibitors
drug effects
γ-aminobutyric acid
Allosteric modulator
Ascorbic acid
Flavonoid
GABA
GABA receptor
N-ethylmaleimide
NEM
Quercetin
Allosteric Regulation
Animals
Ascorbic Acid
Dose-Response Relationship, Drug
GABA-A Receptor Antagonists
Histidine
Humans
Quercetin
Receptors, GABA-A
Allosteric Regulation
Animals
Ascorbic Acid
Dose-Response Relationship, Drug
GABA-A Receptor Antagonists
Histidine
Humans
Quercetin
Receptors, GABA-A
spellingShingle Allosteric modulator
Ascorbic acid
Flavonoid
GABA receptor
Quercetin
4 aminobutyric acid
4 aminobutyric acid A receptor
4 aminobutyric acid A receptor blocking agent
4 aminobutyric acid receptor
ascorbic acid
flavonoid
histidine
quercetin
4 aminobutyric acid A receptor
4 aminobutyric acid A receptor blocking agent
ascorbic acid
quercetin
γ-aminobutyric acid
Allosteric modulator
allosterism
animal
article
chemistry
dose response
drug antagonism
drug effect
human
metabolism
N-ethylmaleimide
NEM
antagonists and inhibitors
drug effects
γ-aminobutyric acid
Allosteric modulator
Ascorbic acid
Flavonoid
GABA
GABA receptor
N-ethylmaleimide
NEM
Quercetin
Allosteric Regulation
Animals
Ascorbic Acid
Dose-Response Relationship, Drug
GABA-A Receptor Antagonists
Histidine
Humans
Quercetin
Receptors, GABA-A
Allosteric Regulation
Animals
Ascorbic Acid
Dose-Response Relationship, Drug
GABA-A Receptor Antagonists
Histidine
Humans
Quercetin
Receptors, GABA-A
Calero, C.I.
González, A.N.B.
Gasulla, J.
Alvarez, S.
Evelson, P.
Calvo, D.J.
Quercetin antagonism of GABAAρ1 receptors is prevented by ascorbic acid through a redox-independent mechanism
topic_facet Allosteric modulator
Ascorbic acid
Flavonoid
GABA receptor
Quercetin
4 aminobutyric acid
4 aminobutyric acid A receptor
4 aminobutyric acid A receptor blocking agent
4 aminobutyric acid receptor
ascorbic acid
flavonoid
histidine
quercetin
4 aminobutyric acid A receptor
4 aminobutyric acid A receptor blocking agent
ascorbic acid
quercetin
γ-aminobutyric acid
Allosteric modulator
allosterism
animal
article
chemistry
dose response
drug antagonism
drug effect
human
metabolism
N-ethylmaleimide
NEM
antagonists and inhibitors
drug effects
γ-aminobutyric acid
Allosteric modulator
Ascorbic acid
Flavonoid
GABA
GABA receptor
N-ethylmaleimide
NEM
Quercetin
Allosteric Regulation
Animals
Ascorbic Acid
Dose-Response Relationship, Drug
GABA-A Receptor Antagonists
Histidine
Humans
Quercetin
Receptors, GABA-A
Allosteric Regulation
Animals
Ascorbic Acid
Dose-Response Relationship, Drug
GABA-A Receptor Antagonists
Histidine
Humans
Quercetin
Receptors, GABA-A
description Quercetin is a natural flavonoid widely distributed in plants that acts as a neuroprotective agent and modulates the activity of different synaptic receptors and ion channels, including the ionotropic GABA receptors. GABA Aρ1 receptors were shown to be antagonized by quercetin, but the mechanisms underlying these antagonistic actions are still unknown. We have analyzed here if the antagonistic action produced by quercetin on GABA Aρ1 receptors was related to its redox activity or due to alternative mechanism/s. Homomeric GABAAρ1 receptors were expressed in frog oocytes and GABA-evoked responses electro-physiologically recorded. Quercetin effects on GABAAρ1 receptors were examined in the absence or presence of ascorbic acid. Chemical protection of cysteines by selective sulfhydryl reagents and site directed mutagenesis experiments were also used to determine ρ1 subunit residues involved in quercetin actions. Quercetin antagonized GABAAρ1 receptor responses in a dose-dependent, fast and reversible manner. Quercetin inhibition was prevented in the presence of ascorbic acid, but not by thiol reagents that modify the extracellular Cys-loop of these receptors. H141, an aminoacidic residue located near to the ρ1 subunit GABA binding site, was involved in the allosteric modulation of GABAAρ1 receptors by several agents including ascorbic acid. Quercetin similarly antagonized GABA-evoked responses mediated by mutant H141DGABAAρ1 and wild-type receptors, but prevention exerted by ascorbic acid on quercetin effects was impaired in mutant receptors. Taken together the present results suggest that quercetin antagonistic actions on GABAAρ1 receptors are mediated through a redox-independent allosteric mechanism. © 2013 Elsevier B.V. All rights reserved.
format JOUR
author Calero, C.I.
González, A.N.B.
Gasulla, J.
Alvarez, S.
Evelson, P.
Calvo, D.J.
author_facet Calero, C.I.
González, A.N.B.
Gasulla, J.
Alvarez, S.
Evelson, P.
Calvo, D.J.
author_sort Calero, C.I.
title Quercetin antagonism of GABAAρ1 receptors is prevented by ascorbic acid through a redox-independent mechanism
title_short Quercetin antagonism of GABAAρ1 receptors is prevented by ascorbic acid through a redox-independent mechanism
title_full Quercetin antagonism of GABAAρ1 receptors is prevented by ascorbic acid through a redox-independent mechanism
title_fullStr Quercetin antagonism of GABAAρ1 receptors is prevented by ascorbic acid through a redox-independent mechanism
title_full_unstemmed Quercetin antagonism of GABAAρ1 receptors is prevented by ascorbic acid through a redox-independent mechanism
title_sort quercetin antagonism of gabaaρ1 receptors is prevented by ascorbic acid through a redox-independent mechanism
url http://hdl.handle.net/20.500.12110/paper_00142999_v714_n1-3_p274_Calero
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