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GABA(A) Receptors Containing ρ1 Subunits Contribute to In Vivo Effects of Ethanol in Mice

GABA(A) receptors consisting of ρ1, ρ2, or ρ3 subunits in homo- or hetero-pentamers have been studied mainly in retina but are detected in many brain regions. Receptors formed from ρ1 are inhibited by low ethanol concentrations, and family-based association analyses have linked ρ subunit genes with...

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Autores principales: Blednov, Yuri A., Benavidez, Jillian M., Black, Mendy, Leiter, Courtney R., Osterndorff-Kahanek, Elizabeth, Johnson, David, Borghese, Cecilia M., Hanrahan, Jane R., Johnston, Graham A. R., Chebib, Mary, Harris, R. Adron
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3894180/
https://www.ncbi.nlm.nih.gov/pubmed/24454882
http://dx.doi.org/10.1371/journal.pone.0085525
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author Blednov, Yuri A.
Benavidez, Jillian M.
Black, Mendy
Leiter, Courtney R.
Osterndorff-Kahanek, Elizabeth
Johnson, David
Borghese, Cecilia M.
Hanrahan, Jane R.
Johnston, Graham A. R.
Chebib, Mary
Harris, R. Adron
author_facet Blednov, Yuri A.
Benavidez, Jillian M.
Black, Mendy
Leiter, Courtney R.
Osterndorff-Kahanek, Elizabeth
Johnson, David
Borghese, Cecilia M.
Hanrahan, Jane R.
Johnston, Graham A. R.
Chebib, Mary
Harris, R. Adron
author_sort Blednov, Yuri A.
collection PubMed
description GABA(A) receptors consisting of ρ1, ρ2, or ρ3 subunits in homo- or hetero-pentamers have been studied mainly in retina but are detected in many brain regions. Receptors formed from ρ1 are inhibited by low ethanol concentrations, and family-based association analyses have linked ρ subunit genes with alcohol dependence. We determined if genetic deletion of ρ1 in mice altered in vivo ethanol effects. Null mutant male mice showed reduced ethanol consumption and preference in a two-bottle choice test with no differences in preference for saccharin or quinine. Null mutant mice of both sexes demonstrated longer duration of ethanol-induced loss of righting reflex (LORR), and males were more sensitive to ethanol-induced motor sedation. In contrast, ρ1 null mice showed faster recovery from acute motor incoordination produced by ethanol. Null mutant females were less sensitive to ethanol-induced development of conditioned taste aversion. Measurement of mRNA levels in cerebellum showed that deletion of ρ1 did not change expression of ρ2, α2, or α6 GABA(A) receptor subunits. (S)-4-amino-cyclopent-1-enyl butylphosphinic acid (“ρ1” antagonist), when administered to wild type mice, mimicked the changes that ethanol induced in ρ1 null mice (LORR and rotarod tests), but the ρ1 antagonist did not produce these effects in ρ1 null mice. In contrast, (R)-4-amino-cyclopent-1-enyl butylphosphinic acid (“ρ2” antagonist) did not change ethanol actions in wild type but produced effects in mice lacking ρ1 that were opposite of the effects of deleting (or inhibiting) ρ1. These results suggest that ρ1 has a predominant role in two in vivo effects of ethanol, and a role for ρ2 may be revealed when ρ1 is deleted. We also found that ethanol produces similar inhibition of function of recombinant ρ1 and ρ2 receptors. These data indicate that ethanol action on GABA(A) receptors containing ρ1/ρ2 subunits may be important for specific effects of ethanol in vivo.
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spelling pubmed-38941802014-01-21 GABA(A) Receptors Containing ρ1 Subunits Contribute to In Vivo Effects of Ethanol in Mice Blednov, Yuri A. Benavidez, Jillian M. Black, Mendy Leiter, Courtney R. Osterndorff-Kahanek, Elizabeth Johnson, David Borghese, Cecilia M. Hanrahan, Jane R. Johnston, Graham A. R. Chebib, Mary Harris, R. Adron PLoS One Research Article GABA(A) receptors consisting of ρ1, ρ2, or ρ3 subunits in homo- or hetero-pentamers have been studied mainly in retina but are detected in many brain regions. Receptors formed from ρ1 are inhibited by low ethanol concentrations, and family-based association analyses have linked ρ subunit genes with alcohol dependence. We determined if genetic deletion of ρ1 in mice altered in vivo ethanol effects. Null mutant male mice showed reduced ethanol consumption and preference in a two-bottle choice test with no differences in preference for saccharin or quinine. Null mutant mice of both sexes demonstrated longer duration of ethanol-induced loss of righting reflex (LORR), and males were more sensitive to ethanol-induced motor sedation. In contrast, ρ1 null mice showed faster recovery from acute motor incoordination produced by ethanol. Null mutant females were less sensitive to ethanol-induced development of conditioned taste aversion. Measurement of mRNA levels in cerebellum showed that deletion of ρ1 did not change expression of ρ2, α2, or α6 GABA(A) receptor subunits. (S)-4-amino-cyclopent-1-enyl butylphosphinic acid (“ρ1” antagonist), when administered to wild type mice, mimicked the changes that ethanol induced in ρ1 null mice (LORR and rotarod tests), but the ρ1 antagonist did not produce these effects in ρ1 null mice. In contrast, (R)-4-amino-cyclopent-1-enyl butylphosphinic acid (“ρ2” antagonist) did not change ethanol actions in wild type but produced effects in mice lacking ρ1 that were opposite of the effects of deleting (or inhibiting) ρ1. These results suggest that ρ1 has a predominant role in two in vivo effects of ethanol, and a role for ρ2 may be revealed when ρ1 is deleted. We also found that ethanol produces similar inhibition of function of recombinant ρ1 and ρ2 receptors. These data indicate that ethanol action on GABA(A) receptors containing ρ1/ρ2 subunits may be important for specific effects of ethanol in vivo. Public Library of Science 2014-01-16 /pmc/articles/PMC3894180/ /pubmed/24454882 http://dx.doi.org/10.1371/journal.pone.0085525 Text en © 2014 Blednov et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Blednov, Yuri A.
Benavidez, Jillian M.
Black, Mendy
Leiter, Courtney R.
Osterndorff-Kahanek, Elizabeth
Johnson, David
Borghese, Cecilia M.
Hanrahan, Jane R.
Johnston, Graham A. R.
Chebib, Mary
Harris, R. Adron
GABA(A) Receptors Containing ρ1 Subunits Contribute to In Vivo Effects of Ethanol in Mice
title GABA(A) Receptors Containing ρ1 Subunits Contribute to In Vivo Effects of Ethanol in Mice
title_full GABA(A) Receptors Containing ρ1 Subunits Contribute to In Vivo Effects of Ethanol in Mice
title_fullStr GABA(A) Receptors Containing ρ1 Subunits Contribute to In Vivo Effects of Ethanol in Mice
title_full_unstemmed GABA(A) Receptors Containing ρ1 Subunits Contribute to In Vivo Effects of Ethanol in Mice
title_short GABA(A) Receptors Containing ρ1 Subunits Contribute to In Vivo Effects of Ethanol in Mice
title_sort gaba(a) receptors containing ρ1 subunits contribute to in vivo effects of ethanol in mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3894180/
https://www.ncbi.nlm.nih.gov/pubmed/24454882
http://dx.doi.org/10.1371/journal.pone.0085525
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