Cargando…

Methamphetamine Self-Administration Elicits Sex-Related Changes in Postsynaptic Glutamate Transmission in the Prefrontal Cortex

Preclinical and clinical research has shown that females are more vulnerable to the rewarding effects of stimulants, and it has been proposed that estrogens may play a role in this enhanced sensitivity; however sex differences in methamphetamine (METH)-induced neuroplasticity have not been explored....

Descripción completa

Detalles Bibliográficos
Autores principales: Pena-Bravo, Jose Ignacio, Penrod, Rachel, Reichel, Carmela M., Lavin, Antonieta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6348447/
https://www.ncbi.nlm.nih.gov/pubmed/30693312
http://dx.doi.org/10.1523/ENEURO.0401-18.2018
_version_ 1783390104015863808
author Pena-Bravo, Jose Ignacio
Penrod, Rachel
Reichel, Carmela M.
Lavin, Antonieta
author_facet Pena-Bravo, Jose Ignacio
Penrod, Rachel
Reichel, Carmela M.
Lavin, Antonieta
author_sort Pena-Bravo, Jose Ignacio
collection PubMed
description Preclinical and clinical research has shown that females are more vulnerable to the rewarding effects of stimulants, and it has been proposed that estrogens may play a role in this enhanced sensitivity; however sex differences in methamphetamine (METH)-induced neuroplasticity have not been explored. To address this gap in knowledge, we recorded from the prelimbic area of the prefrontal cortex (PL-PFC) of male and female rats following long access METH self-administration (SA) and investigated the resulting long-term synaptic neuroadaptations. Males and females took similar amounts of METH during SA; however, female rats exhibit significant synaptic baseline differences when compared to males. Furthermore, females exhibited a significant increase in evoked excitatory currents. This increase in evoked glutamate was correlated with increases in NMDA currents and was not affected by application of a GluN2B selective blocker. We propose that METH SA selectively upregulates GluN2B-lacking NMDA receptors (NMDAR) in the PFC of female rats. Our results may provide a mechanistic explanation for the sex differences reported for METH addiction in females.
format Online
Article
Text
id pubmed-6348447
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Society for Neuroscience
record_format MEDLINE/PubMed
spelling pubmed-63484472019-01-28 Methamphetamine Self-Administration Elicits Sex-Related Changes in Postsynaptic Glutamate Transmission in the Prefrontal Cortex Pena-Bravo, Jose Ignacio Penrod, Rachel Reichel, Carmela M. Lavin, Antonieta eNeuro New Research Preclinical and clinical research has shown that females are more vulnerable to the rewarding effects of stimulants, and it has been proposed that estrogens may play a role in this enhanced sensitivity; however sex differences in methamphetamine (METH)-induced neuroplasticity have not been explored. To address this gap in knowledge, we recorded from the prelimbic area of the prefrontal cortex (PL-PFC) of male and female rats following long access METH self-administration (SA) and investigated the resulting long-term synaptic neuroadaptations. Males and females took similar amounts of METH during SA; however, female rats exhibit significant synaptic baseline differences when compared to males. Furthermore, females exhibited a significant increase in evoked excitatory currents. This increase in evoked glutamate was correlated with increases in NMDA currents and was not affected by application of a GluN2B selective blocker. We propose that METH SA selectively upregulates GluN2B-lacking NMDA receptors (NMDAR) in the PFC of female rats. Our results may provide a mechanistic explanation for the sex differences reported for METH addiction in females. Society for Neuroscience 2019-01-28 /pmc/articles/PMC6348447/ /pubmed/30693312 http://dx.doi.org/10.1523/ENEURO.0401-18.2018 Text en Copyright © 2019 Ignacio Pena-Bravo et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle New Research
Pena-Bravo, Jose Ignacio
Penrod, Rachel
Reichel, Carmela M.
Lavin, Antonieta
Methamphetamine Self-Administration Elicits Sex-Related Changes in Postsynaptic Glutamate Transmission in the Prefrontal Cortex
title Methamphetamine Self-Administration Elicits Sex-Related Changes in Postsynaptic Glutamate Transmission in the Prefrontal Cortex
title_full Methamphetamine Self-Administration Elicits Sex-Related Changes in Postsynaptic Glutamate Transmission in the Prefrontal Cortex
title_fullStr Methamphetamine Self-Administration Elicits Sex-Related Changes in Postsynaptic Glutamate Transmission in the Prefrontal Cortex
title_full_unstemmed Methamphetamine Self-Administration Elicits Sex-Related Changes in Postsynaptic Glutamate Transmission in the Prefrontal Cortex
title_short Methamphetamine Self-Administration Elicits Sex-Related Changes in Postsynaptic Glutamate Transmission in the Prefrontal Cortex
title_sort methamphetamine self-administration elicits sex-related changes in postsynaptic glutamate transmission in the prefrontal cortex
topic New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6348447/
https://www.ncbi.nlm.nih.gov/pubmed/30693312
http://dx.doi.org/10.1523/ENEURO.0401-18.2018
work_keys_str_mv AT penabravojoseignacio methamphetamineselfadministrationelicitssexrelatedchangesinpostsynapticglutamatetransmissionintheprefrontalcortex
AT penrodrachel methamphetamineselfadministrationelicitssexrelatedchangesinpostsynapticglutamatetransmissionintheprefrontalcortex
AT reichelcarmelam methamphetamineselfadministrationelicitssexrelatedchangesinpostsynapticglutamatetransmissionintheprefrontalcortex
AT lavinantonieta methamphetamineselfadministrationelicitssexrelatedchangesinpostsynapticglutamatetransmissionintheprefrontalcortex