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Methamphetamine regulation of activity and topology of ventral midbrain networks

The ventral midbrain supports a variety of functions through the heterogeneity of neurons. Dopaminergic and GABA neurons within this region are particularly susceptible targets of amphetamine-class psychostimulants such as methamphetamine. While this has been evidenced through single-neuron methods,...

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Autores principales: Miller, Douglas R., Lebowitz, Joseph J., Guenther, Dylan T., Refowich, Alexander J., Hansen, Carissa, Maurer, Andrew P., Khoshbouei, Habibeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6752877/
https://www.ncbi.nlm.nih.gov/pubmed/31536584
http://dx.doi.org/10.1371/journal.pone.0222957
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author Miller, Douglas R.
Lebowitz, Joseph J.
Guenther, Dylan T.
Refowich, Alexander J.
Hansen, Carissa
Maurer, Andrew P.
Khoshbouei, Habibeh
author_facet Miller, Douglas R.
Lebowitz, Joseph J.
Guenther, Dylan T.
Refowich, Alexander J.
Hansen, Carissa
Maurer, Andrew P.
Khoshbouei, Habibeh
author_sort Miller, Douglas R.
collection PubMed
description The ventral midbrain supports a variety of functions through the heterogeneity of neurons. Dopaminergic and GABA neurons within this region are particularly susceptible targets of amphetamine-class psychostimulants such as methamphetamine. While this has been evidenced through single-neuron methods, it remains unclear whether and to what extent the local neuronal network is affected and if so, by which mechanisms. Both GABAergic and dopaminergic neurons were heavily featured within the primary ventral midbrain network model system. Using spontaneous calcium activity, our data suggest methamphetamine decreased total network output via a D(2) receptor-dependent manner. Over culture duration, functional connectivity between neurons decreased significantly but was unaffected by methamphetamine. However, across culture duration, exposure to methamphetamine significantly altered changes in network assortativity. Here we have established primary ventral midbrain networks culture as a viable model system that reveals specific changes in network activity, connectivity, and topology modulation by methamphetamine. This network culture system enables control over the type and number of neurons that comprise a network and facilitates detection of emergent properties that arise from the specific organization. Thus, the multidimensional properties of methamphetamine can be unraveled, leading to a better understanding of its impact on the local network structure and function.
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spelling pubmed-67528772019-09-27 Methamphetamine regulation of activity and topology of ventral midbrain networks Miller, Douglas R. Lebowitz, Joseph J. Guenther, Dylan T. Refowich, Alexander J. Hansen, Carissa Maurer, Andrew P. Khoshbouei, Habibeh PLoS One Research Article The ventral midbrain supports a variety of functions through the heterogeneity of neurons. Dopaminergic and GABA neurons within this region are particularly susceptible targets of amphetamine-class psychostimulants such as methamphetamine. While this has been evidenced through single-neuron methods, it remains unclear whether and to what extent the local neuronal network is affected and if so, by which mechanisms. Both GABAergic and dopaminergic neurons were heavily featured within the primary ventral midbrain network model system. Using spontaneous calcium activity, our data suggest methamphetamine decreased total network output via a D(2) receptor-dependent manner. Over culture duration, functional connectivity between neurons decreased significantly but was unaffected by methamphetamine. However, across culture duration, exposure to methamphetamine significantly altered changes in network assortativity. Here we have established primary ventral midbrain networks culture as a viable model system that reveals specific changes in network activity, connectivity, and topology modulation by methamphetamine. This network culture system enables control over the type and number of neurons that comprise a network and facilitates detection of emergent properties that arise from the specific organization. Thus, the multidimensional properties of methamphetamine can be unraveled, leading to a better understanding of its impact on the local network structure and function. Public Library of Science 2019-09-19 /pmc/articles/PMC6752877/ /pubmed/31536584 http://dx.doi.org/10.1371/journal.pone.0222957 Text en © 2019 Miller et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Miller, Douglas R.
Lebowitz, Joseph J.
Guenther, Dylan T.
Refowich, Alexander J.
Hansen, Carissa
Maurer, Andrew P.
Khoshbouei, Habibeh
Methamphetamine regulation of activity and topology of ventral midbrain networks
title Methamphetamine regulation of activity and topology of ventral midbrain networks
title_full Methamphetamine regulation of activity and topology of ventral midbrain networks
title_fullStr Methamphetamine regulation of activity and topology of ventral midbrain networks
title_full_unstemmed Methamphetamine regulation of activity and topology of ventral midbrain networks
title_short Methamphetamine regulation of activity and topology of ventral midbrain networks
title_sort methamphetamine regulation of activity and topology of ventral midbrain networks
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6752877/
https://www.ncbi.nlm.nih.gov/pubmed/31536584
http://dx.doi.org/10.1371/journal.pone.0222957
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