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Modulation of GABA A receptors and of GABAergic synapses by the natural alkaloid gelsemine.

Authors :
Marileo AM
Gavilán J
San Martín VP
Lara CO
Sazo A
Muñoz-Montesino C
Castro PA
Burgos CF
Leiva-Salcedo E
Aguayo LG
Moraga-Cid G
Fuentealba J
Yévenes GE
Source :
Frontiers in molecular neuroscience [Front Mol Neurosci] 2023 Jan 17; Vol. 15, pp. 1083189. Date of Electronic Publication: 2023 Jan 17 (Print Publication: 2022).
Publication Year :
2023

Abstract

The Gelsemium elegans plant preparations have shown beneficial activity against common diseases, including chronic pain and anxiety. Nevertheless, their clinical uses are limited by their toxicity. Gelsemine, one of the most abundant alkaloids in the Gelsemium plants, have replicated these therapeutic and toxic actions in experimental behavioral models. However, the molecular targets underlying these biological effects remain unclear. The behavioral activity profile of gelsemine suggests the involvement of GABA <subscript>A</subscript> receptors (GABA <subscript>A</subscript> Rs), which are the main biological targets of benzodiazepines (BDZs), a group of drugs with anxiolytic, hypnotic, and analgesic properties. Here, we aim to define the modulation of GABA <subscript>A</subscript> Rs by gelsemine, with a special focus on the subtypes involved in the BDZ actions. The gelsemine actions were determined by electrophysiological recordings of recombinant GABA <subscript>A</subscript> Rs expressed in HEK293 cells, and of native receptors in cortical neurons. Gelsemine inhibited the agonist-evoked currents of recombinant and native receptors. The functional inhibition was not associated with the BDZ binding site. We determined in addition that gelsemine diminished the frequency of GABAergic synaptic events, likely through a presynaptic modulation. Our findings establish gelsemine as a negative modulator of GABA <subscript>A</subscript> Rs and of GABAergic synaptic function. These pharmacological features discard direct anxiolytic or analgesic actions of gelsemine through GABA <subscript>A</subscript> Rs but support a role of GABA <subscript>A</subscript> Rs on the alkaloid induced toxicity. On the other hand, the presynaptic effects of the alkaloid provide an additional mechanism to explain their beneficial effects. Collectively, our results contribute novel information to improve understanding of gelsemine actions in the mammalian nervous system.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2023 Marileo, Gavilán, San Martín, Lara, Sazo, Muñoz-Montesino, Castro, Burgos, Leiva-Salcedo, Aguayo, Moraga-Cid, Fuentealba and Yévenes.)

Details

Language :
English
ISSN :
1662-5099
Volume :
15
Database :
MEDLINE
Journal :
Frontiers in molecular neuroscience
Publication Type :
Academic Journal
Accession number :
36733271
Full Text :
https://doi.org/10.3389/fnmol.2022.1083189