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Glutamatergic Neurometabolites during Early Abstinence from Chronic Methamphetamine Abuse

BACKGROUND: The acute phase of abstinence from methamphetamine abuse is critical for rehabilitation success. Proton magnetic resonance spectroscopy has detected below-normal levels of glutamate+glutamine in anterior middle cingulate of chronic methamphetamine abusers during early abstinence, attribu...

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Autores principales: O’Neill, Joseph, Tobias, Marc C., Hudkins, Matthew, London, Edythe D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4360253/
https://www.ncbi.nlm.nih.gov/pubmed/25522400
http://dx.doi.org/10.1093/ijnp/pyu059
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author O’Neill, Joseph
Tobias, Marc C.
Hudkins, Matthew
London, Edythe D.
author_facet O’Neill, Joseph
Tobias, Marc C.
Hudkins, Matthew
London, Edythe D.
author_sort O’Neill, Joseph
collection PubMed
description BACKGROUND: The acute phase of abstinence from methamphetamine abuse is critical for rehabilitation success. Proton magnetic resonance spectroscopy has detected below-normal levels of glutamate+glutamine in anterior middle cingulate of chronic methamphetamine abusers during early abstinence, attributed to abstinence-induced downregulation of the glutamatergic systems in the brain. This study further explored this phenomenon. METHODS: We measured glutamate+glutamine in additional cortical regions (midline posterior cingulate, midline precuneus, and bilateral inferior frontal cortex) putatively affected by methamphetamine. We examined the relationship between glutamate+glutamine in each region with duration of methamphetamine abuse as well as the depressive symptoms of early abstinence. Magnetic resonance spectroscopic imaging was acquired at 1.5 T from a methamphetamine group of 44 adults who had chronically abused methamphetamine and a control group of 23 age-, sex-, and tobacco smoking-matched healthy volunteers. Participants in the methamphetamine group were studied as inpatients during the first week of abstinence from the drug and were not receiving treatment. RESULTS: In the methamphetamine group, small but significant (5–15%, P<.05) decrements (vs control) in glutamate+glutamine were observed in posterior cingulate, precuneus, and right inferior frontal cortex; glutamate+glutamine in posterior cingulate was negatively correlated (P<.05) with years of methamphetamine abuse. The Beck Depression Inventory score was negatively correlated (P<.005) with glutamate+glutamine in right inferior frontal cortex. CONCLUSIONS: Our findings support the idea that glutamatergic metabolism is downregulated in early abstinence in multiple cortical regions. The extent of downregulation may vary with length of abuse and may be associated with severity of depressive symptoms emergent in early recovery.
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spelling pubmed-43602532015-09-01 Glutamatergic Neurometabolites during Early Abstinence from Chronic Methamphetamine Abuse O’Neill, Joseph Tobias, Marc C. Hudkins, Matthew London, Edythe D. Int J Neuropsychopharmacol Research Article BACKGROUND: The acute phase of abstinence from methamphetamine abuse is critical for rehabilitation success. Proton magnetic resonance spectroscopy has detected below-normal levels of glutamate+glutamine in anterior middle cingulate of chronic methamphetamine abusers during early abstinence, attributed to abstinence-induced downregulation of the glutamatergic systems in the brain. This study further explored this phenomenon. METHODS: We measured glutamate+glutamine in additional cortical regions (midline posterior cingulate, midline precuneus, and bilateral inferior frontal cortex) putatively affected by methamphetamine. We examined the relationship between glutamate+glutamine in each region with duration of methamphetamine abuse as well as the depressive symptoms of early abstinence. Magnetic resonance spectroscopic imaging was acquired at 1.5 T from a methamphetamine group of 44 adults who had chronically abused methamphetamine and a control group of 23 age-, sex-, and tobacco smoking-matched healthy volunteers. Participants in the methamphetamine group were studied as inpatients during the first week of abstinence from the drug and were not receiving treatment. RESULTS: In the methamphetamine group, small but significant (5–15%, P<.05) decrements (vs control) in glutamate+glutamine were observed in posterior cingulate, precuneus, and right inferior frontal cortex; glutamate+glutamine in posterior cingulate was negatively correlated (P<.05) with years of methamphetamine abuse. The Beck Depression Inventory score was negatively correlated (P<.005) with glutamate+glutamine in right inferior frontal cortex. CONCLUSIONS: Our findings support the idea that glutamatergic metabolism is downregulated in early abstinence in multiple cortical regions. The extent of downregulation may vary with length of abuse and may be associated with severity of depressive symptoms emergent in early recovery. Oxford University Press 2015-01-24 /pmc/articles/PMC4360253/ /pubmed/25522400 http://dx.doi.org/10.1093/ijnp/pyu059 Text en © The Author 2015. Published by Oxford University Press on behalf of CINP. http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
O’Neill, Joseph
Tobias, Marc C.
Hudkins, Matthew
London, Edythe D.
Glutamatergic Neurometabolites during Early Abstinence from Chronic Methamphetamine Abuse
title Glutamatergic Neurometabolites during Early Abstinence from Chronic Methamphetamine Abuse
title_full Glutamatergic Neurometabolites during Early Abstinence from Chronic Methamphetamine Abuse
title_fullStr Glutamatergic Neurometabolites during Early Abstinence from Chronic Methamphetamine Abuse
title_full_unstemmed Glutamatergic Neurometabolites during Early Abstinence from Chronic Methamphetamine Abuse
title_short Glutamatergic Neurometabolites during Early Abstinence from Chronic Methamphetamine Abuse
title_sort glutamatergic neurometabolites during early abstinence from chronic methamphetamine abuse
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4360253/
https://www.ncbi.nlm.nih.gov/pubmed/25522400
http://dx.doi.org/10.1093/ijnp/pyu059
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