Cargando…

Severe drug-induced repetitive behaviors and striatal overexpression of VAChT in ChAT-ChR2-EYFP BAC transgenic mice

In drug users, drug-related cues alone can induce dopamine release in the dorsal striatum. Instructive cues activate inputs to the striatum from both dopaminergic and cholinergic neurons, which are thought to work together to support motor learning and motivated behaviors. Imbalances in these neurom...

Descripción completa

Detalles Bibliográficos
Autores principales: Crittenden, Jill R., Lacey, Carolyn J., Lee, Tyrone, Bowden, Hilary A., Graybiel, Ann M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4036131/
https://www.ncbi.nlm.nih.gov/pubmed/24904300
http://dx.doi.org/10.3389/fncir.2014.00057
_version_ 1782318138291912704
author Crittenden, Jill R.
Lacey, Carolyn J.
Lee, Tyrone
Bowden, Hilary A.
Graybiel, Ann M.
author_facet Crittenden, Jill R.
Lacey, Carolyn J.
Lee, Tyrone
Bowden, Hilary A.
Graybiel, Ann M.
author_sort Crittenden, Jill R.
collection PubMed
description In drug users, drug-related cues alone can induce dopamine release in the dorsal striatum. Instructive cues activate inputs to the striatum from both dopaminergic and cholinergic neurons, which are thought to work together to support motor learning and motivated behaviors. Imbalances in these neuromodulatory influences can impair normal action selection and might thus contribute to pathologically repetitive and compulsive behaviors such as drug addiction. Dopamine and acetylcholine can have either antagonistic or synergistic effects on behavior, depending on the state of the animal and the receptor signaling systems at play. Semi-synchronized activation of cholinergic interneurons in the dorsal striatum drives dopamine release via presynaptic nicotinic acetylcholine receptors located on dopamine terminals. Nicotinic receptor blockade is known to diminish abnormal repetitive behaviors (stereotypies) induced by psychomotor stimulants. By contrast, blockade of postsynaptic acetylcholine muscarinic receptors in the dorsomedial striatum exacerbates drug-induced stereotypy, exemplifying how different acetylcholine receptors can also have opposing effects. Although acetylcholine release is known to be altered in animal models of drug addiction, predicting whether these changes will augment or diminish drug-induced behaviors thus remains a challenge. Here, we measured amphetamine-induced stereotypy in BAC transgenic mice that have been shown to overexpress the vesicular acetylcholine transporter (VAChT) with consequent increased acetylcholine release. We found that drug-induced stereotypies, consisting of confined sniffing and licking behaviors, were greatly increased in the transgenic mice relative to sibling controls, as was striatal VAChT protein. These findings suggest that VAChT-mediated increases in acetylcholine could be critical in exacerbating drug-induced stereotypic behaviors and promoting exaggerated behavioral fixity.
format Online
Article
Text
id pubmed-4036131
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-40361312014-06-05 Severe drug-induced repetitive behaviors and striatal overexpression of VAChT in ChAT-ChR2-EYFP BAC transgenic mice Crittenden, Jill R. Lacey, Carolyn J. Lee, Tyrone Bowden, Hilary A. Graybiel, Ann M. Front Neural Circuits Neuroscience In drug users, drug-related cues alone can induce dopamine release in the dorsal striatum. Instructive cues activate inputs to the striatum from both dopaminergic and cholinergic neurons, which are thought to work together to support motor learning and motivated behaviors. Imbalances in these neuromodulatory influences can impair normal action selection and might thus contribute to pathologically repetitive and compulsive behaviors such as drug addiction. Dopamine and acetylcholine can have either antagonistic or synergistic effects on behavior, depending on the state of the animal and the receptor signaling systems at play. Semi-synchronized activation of cholinergic interneurons in the dorsal striatum drives dopamine release via presynaptic nicotinic acetylcholine receptors located on dopamine terminals. Nicotinic receptor blockade is known to diminish abnormal repetitive behaviors (stereotypies) induced by psychomotor stimulants. By contrast, blockade of postsynaptic acetylcholine muscarinic receptors in the dorsomedial striatum exacerbates drug-induced stereotypy, exemplifying how different acetylcholine receptors can also have opposing effects. Although acetylcholine release is known to be altered in animal models of drug addiction, predicting whether these changes will augment or diminish drug-induced behaviors thus remains a challenge. Here, we measured amphetamine-induced stereotypy in BAC transgenic mice that have been shown to overexpress the vesicular acetylcholine transporter (VAChT) with consequent increased acetylcholine release. We found that drug-induced stereotypies, consisting of confined sniffing and licking behaviors, were greatly increased in the transgenic mice relative to sibling controls, as was striatal VAChT protein. These findings suggest that VAChT-mediated increases in acetylcholine could be critical in exacerbating drug-induced stereotypic behaviors and promoting exaggerated behavioral fixity. Frontiers Media S.A. 2014-05-28 /pmc/articles/PMC4036131/ /pubmed/24904300 http://dx.doi.org/10.3389/fncir.2014.00057 Text en Copyright © 2014 Crittenden, Lacey, Lee, Bowden and Graybiel. http://creativecommons.org/licenses/by/3.0/ 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) or licensor 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 Neuroscience
Crittenden, Jill R.
Lacey, Carolyn J.
Lee, Tyrone
Bowden, Hilary A.
Graybiel, Ann M.
Severe drug-induced repetitive behaviors and striatal overexpression of VAChT in ChAT-ChR2-EYFP BAC transgenic mice
title Severe drug-induced repetitive behaviors and striatal overexpression of VAChT in ChAT-ChR2-EYFP BAC transgenic mice
title_full Severe drug-induced repetitive behaviors and striatal overexpression of VAChT in ChAT-ChR2-EYFP BAC transgenic mice
title_fullStr Severe drug-induced repetitive behaviors and striatal overexpression of VAChT in ChAT-ChR2-EYFP BAC transgenic mice
title_full_unstemmed Severe drug-induced repetitive behaviors and striatal overexpression of VAChT in ChAT-ChR2-EYFP BAC transgenic mice
title_short Severe drug-induced repetitive behaviors and striatal overexpression of VAChT in ChAT-ChR2-EYFP BAC transgenic mice
title_sort severe drug-induced repetitive behaviors and striatal overexpression of vacht in chat-chr2-eyfp bac transgenic mice
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4036131/
https://www.ncbi.nlm.nih.gov/pubmed/24904300
http://dx.doi.org/10.3389/fncir.2014.00057
work_keys_str_mv AT crittendenjillr severedruginducedrepetitivebehaviorsandstriataloverexpressionofvachtinchatchr2eyfpbactransgenicmice
AT laceycarolynj severedruginducedrepetitivebehaviorsandstriataloverexpressionofvachtinchatchr2eyfpbactransgenicmice
AT leetyrone severedruginducedrepetitivebehaviorsandstriataloverexpressionofvachtinchatchr2eyfpbactransgenicmice
AT bowdenhilarya severedruginducedrepetitivebehaviorsandstriataloverexpressionofvachtinchatchr2eyfpbactransgenicmice
AT graybielannm severedruginducedrepetitivebehaviorsandstriataloverexpressionofvachtinchatchr2eyfpbactransgenicmice