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Evidence That Cannabis Exposure, Abuse, and Dependence Are Related to Glutamate Metabolism and Glial Function in the Anterior Cingulate Cortex: A (1)H-Magnetic Resonance Spectroscopy Study

There is evidence that long-term cannabis use is associated with alterations to glutamate neurotransmission and glial function. In this study, 26 long-term cannabis users (males=65.4%) and 47 non-cannabis using healthy controls (males=44.6%) underwent proton magnetic resonance spectroscopy ((1)H-MRS...

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Autores principales: Watts, Jeremy J., Garani, Ranjini, Da Silva, Tania, Lalang, Nittha, Chavez, Sofia, Mizrahi, Romina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468488/
https://www.ncbi.nlm.nih.gov/pubmed/32973572
http://dx.doi.org/10.3389/fpsyt.2020.00764
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author Watts, Jeremy J.
Garani, Ranjini
Da Silva, Tania
Lalang, Nittha
Chavez, Sofia
Mizrahi, Romina
author_facet Watts, Jeremy J.
Garani, Ranjini
Da Silva, Tania
Lalang, Nittha
Chavez, Sofia
Mizrahi, Romina
author_sort Watts, Jeremy J.
collection PubMed
description There is evidence that long-term cannabis use is associated with alterations to glutamate neurotransmission and glial function. In this study, 26 long-term cannabis users (males=65.4%) and 47 non-cannabis using healthy controls (males=44.6%) underwent proton magnetic resonance spectroscopy ((1)H-MRS) of the anterior cingulate cortex (ACC) in order to characterize neurometabolite alterations in cannabis users and to examine associations between neurometabolites, cannabis exposure, and cannabis use behaviors. Myo-inositol, a marker of glial function, and glutamate metabolites did not differ between healthy controls and cannabis users or cannabis users who met criteria for DSM5 cannabis use disorder (n=17). Lower myo-inositol, a putative marker of glial function, was related to greater problematic drug use (F(1,22) = 11.95, p=.002; Cohen’s f=0.59, large effect; Drug Abuse Screening Test) and severity of cannabis dependence (F(1,22) = 6.61, p=.17; Cohen’s f=0.44, large effect). Further, past-year cannabis exposure exerted different effects on glutamate and glutamate+glutamine in males and females (glutamate: F(1,21) = 6.31, p=.02; glutamate+glutamine: F(1,21) = 7.20, p=.014), such that greater past-year cannabis exposure was related to higher concentrations of glutamate metabolites in male cannabis users (glutamate: F(1,14) = 25.94, p=.00016; Cohen’s f=1.32, large effect; glutamate+glutamine: F(1,14) = 23.24, p=.00027, Cohen’s f=1.24, large effect) but not in female cannabis users (glutamate: F(1,6) = 1.37, p=0.78; glutamate+glutamine: F(1,6) = 0.001, p=.97). The present results extend existing evidence of altered glial function and glutamate metabolism with cannabis use by providing evidence linking problematic drug use behaviors with glial function as measured with myo-inositol and recent chronic cannabis exposure to alterations in glutamate metabolism. This provides novel directions for the interrogation of the impact of cannabis use on brain neurochemistry.
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spelling pubmed-74684882020-09-23 Evidence That Cannabis Exposure, Abuse, and Dependence Are Related to Glutamate Metabolism and Glial Function in the Anterior Cingulate Cortex: A (1)H-Magnetic Resonance Spectroscopy Study Watts, Jeremy J. Garani, Ranjini Da Silva, Tania Lalang, Nittha Chavez, Sofia Mizrahi, Romina Front Psychiatry Psychiatry There is evidence that long-term cannabis use is associated with alterations to glutamate neurotransmission and glial function. In this study, 26 long-term cannabis users (males=65.4%) and 47 non-cannabis using healthy controls (males=44.6%) underwent proton magnetic resonance spectroscopy ((1)H-MRS) of the anterior cingulate cortex (ACC) in order to characterize neurometabolite alterations in cannabis users and to examine associations between neurometabolites, cannabis exposure, and cannabis use behaviors. Myo-inositol, a marker of glial function, and glutamate metabolites did not differ between healthy controls and cannabis users or cannabis users who met criteria for DSM5 cannabis use disorder (n=17). Lower myo-inositol, a putative marker of glial function, was related to greater problematic drug use (F(1,22) = 11.95, p=.002; Cohen’s f=0.59, large effect; Drug Abuse Screening Test) and severity of cannabis dependence (F(1,22) = 6.61, p=.17; Cohen’s f=0.44, large effect). Further, past-year cannabis exposure exerted different effects on glutamate and glutamate+glutamine in males and females (glutamate: F(1,21) = 6.31, p=.02; glutamate+glutamine: F(1,21) = 7.20, p=.014), such that greater past-year cannabis exposure was related to higher concentrations of glutamate metabolites in male cannabis users (glutamate: F(1,14) = 25.94, p=.00016; Cohen’s f=1.32, large effect; glutamate+glutamine: F(1,14) = 23.24, p=.00027, Cohen’s f=1.24, large effect) but not in female cannabis users (glutamate: F(1,6) = 1.37, p=0.78; glutamate+glutamine: F(1,6) = 0.001, p=.97). The present results extend existing evidence of altered glial function and glutamate metabolism with cannabis use by providing evidence linking problematic drug use behaviors with glial function as measured with myo-inositol and recent chronic cannabis exposure to alterations in glutamate metabolism. This provides novel directions for the interrogation of the impact of cannabis use on brain neurochemistry. Frontiers Media S.A. 2020-08-20 /pmc/articles/PMC7468488/ /pubmed/32973572 http://dx.doi.org/10.3389/fpsyt.2020.00764 Text en Copyright © 2020 Watts, Garani, Da Silva, Lalang, Chavez and Mizrahi http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Psychiatry
Watts, Jeremy J.
Garani, Ranjini
Da Silva, Tania
Lalang, Nittha
Chavez, Sofia
Mizrahi, Romina
Evidence That Cannabis Exposure, Abuse, and Dependence Are Related to Glutamate Metabolism and Glial Function in the Anterior Cingulate Cortex: A (1)H-Magnetic Resonance Spectroscopy Study
title Evidence That Cannabis Exposure, Abuse, and Dependence Are Related to Glutamate Metabolism and Glial Function in the Anterior Cingulate Cortex: A (1)H-Magnetic Resonance Spectroscopy Study
title_full Evidence That Cannabis Exposure, Abuse, and Dependence Are Related to Glutamate Metabolism and Glial Function in the Anterior Cingulate Cortex: A (1)H-Magnetic Resonance Spectroscopy Study
title_fullStr Evidence That Cannabis Exposure, Abuse, and Dependence Are Related to Glutamate Metabolism and Glial Function in the Anterior Cingulate Cortex: A (1)H-Magnetic Resonance Spectroscopy Study
title_full_unstemmed Evidence That Cannabis Exposure, Abuse, and Dependence Are Related to Glutamate Metabolism and Glial Function in the Anterior Cingulate Cortex: A (1)H-Magnetic Resonance Spectroscopy Study
title_short Evidence That Cannabis Exposure, Abuse, and Dependence Are Related to Glutamate Metabolism and Glial Function in the Anterior Cingulate Cortex: A (1)H-Magnetic Resonance Spectroscopy Study
title_sort evidence that cannabis exposure, abuse, and dependence are related to glutamate metabolism and glial function in the anterior cingulate cortex: a (1)h-magnetic resonance spectroscopy study
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468488/
https://www.ncbi.nlm.nih.gov/pubmed/32973572
http://dx.doi.org/10.3389/fpsyt.2020.00764
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