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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...
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/PMC9027322/ https://www.ncbi.nlm.nih.gov/pubmed/35457170 http://dx.doi.org/10.3390/ijms23084353 |
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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 |
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