Cargando…

Sex-Specific Alterations in Dopamine Metabolism in the Brain after Methamphetamine Self-Administration

Methamphetamine (METH) use disorder affects both sexes, with sex differences occurring in behavioral, structural, and biochemical consequences. The molecular mechanisms underlying these differences are unclear. Herein, we used a rat model to identify potential sex differences in the effects of METH...

Descripción completa

Detalles Bibliográficos
Autores principales: Daiwile, Atul P., Sullivan, Patricia, Jayanthi, Subramaniam, Goldstein, David S., Cadet, Jean Lud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9027322/
https://www.ncbi.nlm.nih.gov/pubmed/35457170
http://dx.doi.org/10.3390/ijms23084353
_version_ 1784691334386286592
author Daiwile, Atul P.
Sullivan, Patricia
Jayanthi, Subramaniam
Goldstein, David S.
Cadet, Jean Lud
author_facet Daiwile, Atul P.
Sullivan, Patricia
Jayanthi, Subramaniam
Goldstein, David S.
Cadet, Jean Lud
author_sort Daiwile, Atul P.
collection PubMed
description Methamphetamine (METH) use disorder affects both sexes, with sex differences occurring in behavioral, structural, and biochemical consequences. The molecular mechanisms underlying these differences are unclear. Herein, we used a rat model to identify potential sex differences in the effects of METH on brain dopaminergic systems. Rats were trained to self-administer METH for 20 days, and a cue-induced drug-seeking test was performed on withdrawal days 3 and 30. Dopamine and its metabolites were measured in the prefrontal cortex (PFC), nucleus accumbens (NAc), dorsal striatum (dSTR), and hippocampus (HIP). Irrespective of conditions, in comparison to females, male rats showed increased 3,4-dihydroxyphenylalanine (DOPA) in the PFC, dSTR, and HIP; increased cys-dopamine in NAc; and increased 3,4-dihydroxyphenylethanol (DOPET) and 3,4-dihydroxyphenylacetic acid (DOPAC) in dSTR. Males also showed METH-associated decreases in DA levels in the HIP but increases in the NAc. Female rats showed METH-associated decreases in DA, DOPAL, and DOPAC levels in the PFC but increases in DOPET and DOPAC levels in the HIP. Both sexes showed METH-associated decreases in NAc DA metabolites. Together, these data document sex differences in METH SA-induced changes in DA metabolism. These observations provide further support for using sex as an essential variable when discussing therapeutic approaches against METH use disorder in humans.
format Online
Article
Text
id pubmed-9027322
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-90273222022-04-23 Sex-Specific Alterations in Dopamine Metabolism in the Brain after Methamphetamine Self-Administration Daiwile, Atul P. Sullivan, Patricia Jayanthi, Subramaniam Goldstein, David S. Cadet, Jean Lud Int J Mol Sci Article Methamphetamine (METH) use disorder affects both sexes, with sex differences occurring in behavioral, structural, and biochemical consequences. The molecular mechanisms underlying these differences are unclear. Herein, we used a rat model to identify potential sex differences in the effects of METH on brain dopaminergic systems. Rats were trained to self-administer METH for 20 days, and a cue-induced drug-seeking test was performed on withdrawal days 3 and 30. Dopamine and its metabolites were measured in the prefrontal cortex (PFC), nucleus accumbens (NAc), dorsal striatum (dSTR), and hippocampus (HIP). Irrespective of conditions, in comparison to females, male rats showed increased 3,4-dihydroxyphenylalanine (DOPA) in the PFC, dSTR, and HIP; increased cys-dopamine in NAc; and increased 3,4-dihydroxyphenylethanol (DOPET) and 3,4-dihydroxyphenylacetic acid (DOPAC) in dSTR. Males also showed METH-associated decreases in DA levels in the HIP but increases in the NAc. Female rats showed METH-associated decreases in DA, DOPAL, and DOPAC levels in the PFC but increases in DOPET and DOPAC levels in the HIP. Both sexes showed METH-associated decreases in NAc DA metabolites. Together, these data document sex differences in METH SA-induced changes in DA metabolism. These observations provide further support for using sex as an essential variable when discussing therapeutic approaches against METH use disorder in humans. MDPI 2022-04-14 /pmc/articles/PMC9027322/ /pubmed/35457170 http://dx.doi.org/10.3390/ijms23084353 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
Daiwile, Atul P.
Sullivan, Patricia
Jayanthi, Subramaniam
Goldstein, David S.
Cadet, Jean Lud
Sex-Specific Alterations in Dopamine Metabolism in the Brain after Methamphetamine Self-Administration
title Sex-Specific Alterations in Dopamine Metabolism in the Brain after Methamphetamine Self-Administration
title_full Sex-Specific Alterations in Dopamine Metabolism in the Brain after Methamphetamine Self-Administration
title_fullStr Sex-Specific Alterations in Dopamine Metabolism in the Brain after Methamphetamine Self-Administration
title_full_unstemmed Sex-Specific Alterations in Dopamine Metabolism in the Brain after Methamphetamine Self-Administration
title_short Sex-Specific Alterations in Dopamine Metabolism in the Brain after Methamphetamine Self-Administration
title_sort sex-specific alterations in dopamine metabolism in the brain after methamphetamine self-administration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9027322/
https://www.ncbi.nlm.nih.gov/pubmed/35457170
http://dx.doi.org/10.3390/ijms23084353
work_keys_str_mv AT daiwileatulp sexspecificalterationsindopaminemetabolisminthebrainaftermethamphetamineselfadministration
AT sullivanpatricia sexspecificalterationsindopaminemetabolisminthebrainaftermethamphetamineselfadministration
AT jayanthisubramaniam sexspecificalterationsindopaminemetabolisminthebrainaftermethamphetamineselfadministration
AT goldsteindavids sexspecificalterationsindopaminemetabolisminthebrainaftermethamphetamineselfadministration
AT cadetjeanlud sexspecificalterationsindopaminemetabolisminthebrainaftermethamphetamineselfadministration