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Xenopus Oocytes: A Tool to Decipher Molecular Specificity of Insecticides towards Mammalian and Insect GABA—A Receptors
The number of insect GABA receptors (GABAr) available for expression studies has been recently increased by the cloning of the Acyrthosiphon pisum (pea aphid) RDL subunits. This large number of cloned RDL subunits from pest and beneficial insects opens the door to parallel pharmacological studies on...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9146934/ https://www.ncbi.nlm.nih.gov/pubmed/35629767 http://dx.doi.org/10.3390/membranes12050440 |
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author | Bertaud, Anaïs Cens, Thierry Mary, Rosanna Rousset, Matthieu Arel, Elodie Thibaud, Jean-Baptiste Vignes, Michel Ménard, Claudine Dutertre, Sébastien Collet, Claude Charnet, Pierre |
author_facet | Bertaud, Anaïs Cens, Thierry Mary, Rosanna Rousset, Matthieu Arel, Elodie Thibaud, Jean-Baptiste Vignes, Michel Ménard, Claudine Dutertre, Sébastien Collet, Claude Charnet, Pierre |
author_sort | Bertaud, Anaïs |
collection | PubMed |
description | The number of insect GABA receptors (GABAr) available for expression studies has been recently increased by the cloning of the Acyrthosiphon pisum (pea aphid) RDL subunits. This large number of cloned RDL subunits from pest and beneficial insects opens the door to parallel pharmacological studies on the sensitivity of these different insect GABAr to various agonists or antagonists. The resulting analysis of the molecular basis of the species-specific GABAr responses to insecticides is necessary not only to depict and understand species toxicity, but also to help at the early identification of unacceptable toxicity of insecticides toward beneficial insects such as Apis mellifera (honeybees). Using heterologous expression in Xenopus laevis oocytes, and two-electrode voltage-clamp recording to assess the properties of the GABAr, we performed a comparative analysis of the pharmacological sensitivity of RDL subunits from A. pisum, A. mellifera and Varroa destructor GABAr to three pesticides (fipronil, picrotoxin and dieldrin). These data were compared to similar characterizations performed on two Homo sapiens GABA-A receptors (α(2)β(2)γ(2) and α(2)β(2)γ(2)). Our results underline a global conservation of the pharmacological profiles of these receptors, with some interesting species specificities, nonetheless, and suggest that this approach can be useful for the early identification of poorly specific molecules. |
format | Online Article Text |
id | pubmed-9146934 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-91469342022-05-29 Xenopus Oocytes: A Tool to Decipher Molecular Specificity of Insecticides towards Mammalian and Insect GABA—A Receptors Bertaud, Anaïs Cens, Thierry Mary, Rosanna Rousset, Matthieu Arel, Elodie Thibaud, Jean-Baptiste Vignes, Michel Ménard, Claudine Dutertre, Sébastien Collet, Claude Charnet, Pierre Membranes (Basel) Article The number of insect GABA receptors (GABAr) available for expression studies has been recently increased by the cloning of the Acyrthosiphon pisum (pea aphid) RDL subunits. This large number of cloned RDL subunits from pest and beneficial insects opens the door to parallel pharmacological studies on the sensitivity of these different insect GABAr to various agonists or antagonists. The resulting analysis of the molecular basis of the species-specific GABAr responses to insecticides is necessary not only to depict and understand species toxicity, but also to help at the early identification of unacceptable toxicity of insecticides toward beneficial insects such as Apis mellifera (honeybees). Using heterologous expression in Xenopus laevis oocytes, and two-electrode voltage-clamp recording to assess the properties of the GABAr, we performed a comparative analysis of the pharmacological sensitivity of RDL subunits from A. pisum, A. mellifera and Varroa destructor GABAr to three pesticides (fipronil, picrotoxin and dieldrin). These data were compared to similar characterizations performed on two Homo sapiens GABA-A receptors (α(2)β(2)γ(2) and α(2)β(2)γ(2)). Our results underline a global conservation of the pharmacological profiles of these receptors, with some interesting species specificities, nonetheless, and suggest that this approach can be useful for the early identification of poorly specific molecules. MDPI 2022-04-19 /pmc/articles/PMC9146934/ /pubmed/35629767 http://dx.doi.org/10.3390/membranes12050440 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Bertaud, Anaïs Cens, Thierry Mary, Rosanna Rousset, Matthieu Arel, Elodie Thibaud, Jean-Baptiste Vignes, Michel Ménard, Claudine Dutertre, Sébastien Collet, Claude Charnet, Pierre Xenopus Oocytes: A Tool to Decipher Molecular Specificity of Insecticides towards Mammalian and Insect GABA—A Receptors |
title | Xenopus Oocytes: A Tool to Decipher Molecular Specificity of Insecticides towards Mammalian and Insect GABA—A Receptors |
title_full | Xenopus Oocytes: A Tool to Decipher Molecular Specificity of Insecticides towards Mammalian and Insect GABA—A Receptors |
title_fullStr | Xenopus Oocytes: A Tool to Decipher Molecular Specificity of Insecticides towards Mammalian and Insect GABA—A Receptors |
title_full_unstemmed | Xenopus Oocytes: A Tool to Decipher Molecular Specificity of Insecticides towards Mammalian and Insect GABA—A Receptors |
title_short | Xenopus Oocytes: A Tool to Decipher Molecular Specificity of Insecticides towards Mammalian and Insect GABA—A Receptors |
title_sort | xenopus oocytes: a tool to decipher molecular specificity of insecticides towards mammalian and insect gaba—a receptors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9146934/ https://www.ncbi.nlm.nih.gov/pubmed/35629767 http://dx.doi.org/10.3390/membranes12050440 |
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