Parabens inhibit hNaV 1.2 channels

Propylparaben, a commonly used antimicrobial preservative, has been reported as an anticonvulsant agent targeting neuronal Na+ channels (NaV). However, the specific features of the NaV channel inhibition by this agent have so far not been extensively studied. Moreover, it is still unclear if it shar...

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Detalles Bibliográficos
Autores principales: Enrique, Andrea Verónica, Martín, Pedro, Sbaraglini, María Laura, Talevi, Alan, Milesi, María Verónica
Formato: Articulo
Lenguaje:Inglés
Publicado: 2020
Materias:
Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/119488
Aporte de:
id I19-R120-10915-119488
record_format dspace
institution Universidad Nacional de La Plata
institution_str I-19
repository_str R-120
collection SEDICI (UNLP)
language Inglés
topic Biología
Propylparaben
Benzylparaben
Sodium channels
hNaV 1.2
Anticonvulsant drugs
spellingShingle Biología
Propylparaben
Benzylparaben
Sodium channels
hNaV 1.2
Anticonvulsant drugs
Enrique, Andrea Verónica
Martín, Pedro
Sbaraglini, María Laura
Talevi, Alan
Milesi, María Verónica
Parabens inhibit hNaV 1.2 channels
topic_facet Biología
Propylparaben
Benzylparaben
Sodium channels
hNaV 1.2
Anticonvulsant drugs
description Propylparaben, a commonly used antimicrobial preservative, has been reported as an anticonvulsant agent targeting neuronal Na+ channels (NaV). However, the specific features of the NaV channel inhibition by this agent have so far not been extensively studied. Moreover, it is still unclear if it shares this pharmacological activity with other parabens. Here, we fully characterized the mechanism of action of the inhibitory effect that propylparaben and benzylparaben induce on human NaV 1.2 channel isoform (hNaV1.2). We established a first approach to know the parabens structural determinants for this channel inhibition. The parabens effects on hNaV1.2 channel mediated currents were recorded using the patch-clamp whole-cell configuration on hNaV1.2 stably transfected HEK293 cells. Propylparaben induced a typical state-dependent inhibition on hNaV1.2 channel carried current, characterized by a left-shift in the steady-state inactivation curve, a prolongation in the time needed for recovery from fast inactivation and a frequency-dependent blocking behavior. The state-dependent inhibition is increased for butylparaben and benzylparaben and diminished for methylparaben, ethylparaben and p-hydroxybenzoic acid (the major metabolite of parabens hydrolysis). Particularly, butylparaben and benzylparaben shift the steady-state inactivation curve 2- and 3-times more than propylparaben, respectively. Parabens are blockers of hNaV1.2 channels, sharing the mechanism of action of most of sodium channel blocking antiseizure drugs. The potency of this inhibition increases with the size of the lipophilic alcoholic residue of the ester group. These results provide a basis for rational drug design directed to generate new potential anticonvulsant agents.
format Articulo
Articulo
author Enrique, Andrea Verónica
Martín, Pedro
Sbaraglini, María Laura
Talevi, Alan
Milesi, María Verónica
author_facet Enrique, Andrea Verónica
Martín, Pedro
Sbaraglini, María Laura
Talevi, Alan
Milesi, María Verónica
author_sort Enrique, Andrea Verónica
title Parabens inhibit hNaV 1.2 channels
title_short Parabens inhibit hNaV 1.2 channels
title_full Parabens inhibit hNaV 1.2 channels
title_fullStr Parabens inhibit hNaV 1.2 channels
title_full_unstemmed Parabens inhibit hNaV 1.2 channels
title_sort parabens inhibit hnav 1.2 channels
publishDate 2020
url http://sedici.unlp.edu.ar/handle/10915/119488
work_keys_str_mv AT enriqueandreaveronica parabensinhibithnav12channels
AT martinpedro parabensinhibithnav12channels
AT sbaraglinimarialaura parabensinhibithnav12channels
AT talevialan parabensinhibithnav12channels
AT milesimariaveronica parabensinhibithnav12channels
bdutipo_str Repositorios
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