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Glutamate dynamics in the dorsolateral striatum of rats with goal-directed and habitual cocaine-seeking behavior

The shift from drug abuse to addiction is considered to arise from the transition between goal-directed and habitual control over drug behavior. Habitual responding for appetitive and skill-based behaviors is mediated by potentiated glutamate signaling in the dorsolateral striatum (DLS), but the sta...

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Autores principales: Giangrasso, Danielle M., Veros, Kaliana M., Timm, Maureen M., West, Peter J., Wilcox, Karen S., Keefe, Kristen A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10213946/
https://www.ncbi.nlm.nih.gov/pubmed/37251646
http://dx.doi.org/10.3389/fnmol.2023.1160157
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author Giangrasso, Danielle M.
Veros, Kaliana M.
Timm, Maureen M.
West, Peter J.
Wilcox, Karen S.
Keefe, Kristen A.
author_facet Giangrasso, Danielle M.
Veros, Kaliana M.
Timm, Maureen M.
West, Peter J.
Wilcox, Karen S.
Keefe, Kristen A.
author_sort Giangrasso, Danielle M.
collection PubMed
description The shift from drug abuse to addiction is considered to arise from the transition between goal-directed and habitual control over drug behavior. Habitual responding for appetitive and skill-based behaviors is mediated by potentiated glutamate signaling in the dorsolateral striatum (DLS), but the state of the DLS glutamate system in the context of habitual drug-behavior remains undefined. Evidence from the nucleus accumbens of cocaine-experienced rats suggests that decreased transporter-mediated glutamate clearance and enhanced synaptic glutamate release contribute to the potentiated glutamate signaling that underlies the enduring vulnerability to relapse. Preliminary evidence from the dorsal striatum of cocaine-experienced rats suggests that this region exhibits similar alterations to glutamate clearance and release, but it is not known whether these glutamate dynamics are associated with goal-directed or habitual control over cocaine-seeking behavior. Therefore, we trained rats to self-administer cocaine in a chained cocaine-seeking and -taking paradigm, which yielded goal-directed, intermediate, and habitual cocaine-seeking rats. We then assessed glutamate clearance and release dynamics in the DLS of these rats using two different methods: synaptic transporter current (STC) recordings of patch-clamped astrocytes and the intensity-based glutamate sensing fluorescent reporter (iGluSnFr). While we observed a decreased rate of glutamate clearance in STCs evoked with single-pulse stimulation in cocaine-experienced rats, we did not observe any cocaine-induced differences in glutamate clearance rates from STCs evoked with high frequency stimulation (HFS) or iGluSnFr responses evoked with either double-pulse stimulation or HFS. Furthermore, GLT-1 protein expression in the DLS was unchanged in cocaine-experienced rats, regardless of their mode of control over cocaine-seeking behavior. Lastly, there were no differences in metrics of glutamate release between cocaine-experienced rats and yoked-saline controls in either assay. Together, these results suggest that glutamate clearance and release dynamics in the DLS are largely unaltered by a history of cocaine self-administration on this established cocaine seeking-taking paradigm, regardless of whether the control over the cocaine seeking behavior was habitual or goal directed.
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spelling pubmed-102139462023-05-27 Glutamate dynamics in the dorsolateral striatum of rats with goal-directed and habitual cocaine-seeking behavior Giangrasso, Danielle M. Veros, Kaliana M. Timm, Maureen M. West, Peter J. Wilcox, Karen S. Keefe, Kristen A. Front Mol Neurosci Molecular Neuroscience The shift from drug abuse to addiction is considered to arise from the transition between goal-directed and habitual control over drug behavior. Habitual responding for appetitive and skill-based behaviors is mediated by potentiated glutamate signaling in the dorsolateral striatum (DLS), but the state of the DLS glutamate system in the context of habitual drug-behavior remains undefined. Evidence from the nucleus accumbens of cocaine-experienced rats suggests that decreased transporter-mediated glutamate clearance and enhanced synaptic glutamate release contribute to the potentiated glutamate signaling that underlies the enduring vulnerability to relapse. Preliminary evidence from the dorsal striatum of cocaine-experienced rats suggests that this region exhibits similar alterations to glutamate clearance and release, but it is not known whether these glutamate dynamics are associated with goal-directed or habitual control over cocaine-seeking behavior. Therefore, we trained rats to self-administer cocaine in a chained cocaine-seeking and -taking paradigm, which yielded goal-directed, intermediate, and habitual cocaine-seeking rats. We then assessed glutamate clearance and release dynamics in the DLS of these rats using two different methods: synaptic transporter current (STC) recordings of patch-clamped astrocytes and the intensity-based glutamate sensing fluorescent reporter (iGluSnFr). While we observed a decreased rate of glutamate clearance in STCs evoked with single-pulse stimulation in cocaine-experienced rats, we did not observe any cocaine-induced differences in glutamate clearance rates from STCs evoked with high frequency stimulation (HFS) or iGluSnFr responses evoked with either double-pulse stimulation or HFS. Furthermore, GLT-1 protein expression in the DLS was unchanged in cocaine-experienced rats, regardless of their mode of control over cocaine-seeking behavior. Lastly, there were no differences in metrics of glutamate release between cocaine-experienced rats and yoked-saline controls in either assay. Together, these results suggest that glutamate clearance and release dynamics in the DLS are largely unaltered by a history of cocaine self-administration on this established cocaine seeking-taking paradigm, regardless of whether the control over the cocaine seeking behavior was habitual or goal directed. Frontiers Media S.A. 2023-05-11 /pmc/articles/PMC10213946/ /pubmed/37251646 http://dx.doi.org/10.3389/fnmol.2023.1160157 Text en Copyright © 2023 Giangrasso, Veros, Timm, West, Wilcox and Keefe. https://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 Molecular Neuroscience
Giangrasso, Danielle M.
Veros, Kaliana M.
Timm, Maureen M.
West, Peter J.
Wilcox, Karen S.
Keefe, Kristen A.
Glutamate dynamics in the dorsolateral striatum of rats with goal-directed and habitual cocaine-seeking behavior
title Glutamate dynamics in the dorsolateral striatum of rats with goal-directed and habitual cocaine-seeking behavior
title_full Glutamate dynamics in the dorsolateral striatum of rats with goal-directed and habitual cocaine-seeking behavior
title_fullStr Glutamate dynamics in the dorsolateral striatum of rats with goal-directed and habitual cocaine-seeking behavior
title_full_unstemmed Glutamate dynamics in the dorsolateral striatum of rats with goal-directed and habitual cocaine-seeking behavior
title_short Glutamate dynamics in the dorsolateral striatum of rats with goal-directed and habitual cocaine-seeking behavior
title_sort glutamate dynamics in the dorsolateral striatum of rats with goal-directed and habitual cocaine-seeking behavior
topic Molecular Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10213946/
https://www.ncbi.nlm.nih.gov/pubmed/37251646
http://dx.doi.org/10.3389/fnmol.2023.1160157
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