Coordination of Brain-Wide Activity Dynamics by Dopaminergic Neurons
Several neuropsychiatric conditions, such as addiction and schizophrenia, may arise in part from dysregulated activity of ventral tegmental area dopaminergic (TH ) neurons, as well as from more global maladaptation in neurocircuit function. However, whether TH activity affects large-scale brain-wide...
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creator | Decot, Heather K Namboodiri, Vijay M K Gao, Wei McHenry, Jenna A Jennings, Joshua H Lee, Sung-Ho Kantak, Pranish A Jill Kao, Yu-Chieh Das, Manasmita Witten, Ilana B Deisseroth, Karl Shih, Yen-Yu Ian Stuber, Garret D |
description | Several neuropsychiatric conditions, such as addiction and schizophrenia, may arise in part from dysregulated activity of ventral tegmental area dopaminergic (TH
) neurons, as well as from more global maladaptation in neurocircuit function. However, whether TH
activity affects large-scale brain-wide function remains unknown. Here we selectively activated TH
neurons in transgenic rats and measured resulting changes in whole-brain activity using stimulus-evoked functional magnetic resonance imaging. Applying a standard generalized linear model analysis approach, our results indicate that selective optogenetic stimulation of TH
neurons enhanced cerebral blood volume signals in striatal target regions in a dopamine receptor-dependent manner. However, brain-wide voxel-based principal component analysis of the same data set revealed that dopaminergic modulation activates several additional anatomically distinct regions throughout the brain, not typically associated with dopamine release events. Furthermore, explicit pairing of TH
neuronal activation with a forepaw stimulus of a particular frequency expanded the sensory representation of that stimulus, not exclusively within the somatosensory cortices, but brain-wide. These data suggest that modulation of TH
neurons can impact brain dynamics across many distributed anatomically distinct regions, even those that receive little to no direct TH
input. |
doi_str_mv | 10.1038/npp.2016.151 |
format | Article |
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) neurons, as well as from more global maladaptation in neurocircuit function. However, whether TH
activity affects large-scale brain-wide function remains unknown. Here we selectively activated TH
neurons in transgenic rats and measured resulting changes in whole-brain activity using stimulus-evoked functional magnetic resonance imaging. Applying a standard generalized linear model analysis approach, our results indicate that selective optogenetic stimulation of TH
neurons enhanced cerebral blood volume signals in striatal target regions in a dopamine receptor-dependent manner. However, brain-wide voxel-based principal component analysis of the same data set revealed that dopaminergic modulation activates several additional anatomically distinct regions throughout the brain, not typically associated with dopamine release events. Furthermore, explicit pairing of TH
neuronal activation with a forepaw stimulus of a particular frequency expanded the sensory representation of that stimulus, not exclusively within the somatosensory cortices, but brain-wide. These data suggest that modulation of TH
neurons can impact brain dynamics across many distributed anatomically distinct regions, even those that receive little to no direct TH
input.</description><identifier>ISSN: 0893-133X</identifier><identifier>EISSN: 1740-634X</identifier><identifier>DOI: 10.1038/npp.2016.151</identifier><identifier>PMID: 27515791</identifier><identifier>CODEN: NEROEW</identifier><language>eng</language><publisher>England: Nature Publishing Group</publisher><subject>Addictions ; Animals ; Benzazepines - administration & dosage ; Benzazepines - pharmacology ; Biomedical engineering ; Brain - diagnostic imaging ; Brain - drug effects ; Brain - physiology ; Brain research ; Cerebrovascular Circulation - drug effects ; Cerebrovascular Circulation - physiology ; Dopamine ; Dopamine - metabolism ; Dopaminergic Neurons - physiology ; Functional Neuroimaging - methods ; Generalized linear models ; Magnetic resonance imaging ; Magnetic Resonance Imaging - methods ; Male ; Neurosciences ; Original ; Physiology ; Rats ; Rats, Long-Evans ; Receptors, Dopamine D1 - antagonists & inhibitors ; Ventral Tegmental Area - diagnostic imaging ; Ventral Tegmental Area - drug effects ; Ventral Tegmental Area - physiology</subject><ispartof>Neuropsychopharmacology (New York, N.Y.), 2017-02, Vol.42 (3), p.615-627</ispartof><rights>Copyright Nature Publishing Group Feb 2017</rights><rights>Copyright © 2017 American College of Neuropsychopharmacology 2017 American College of Neuropsychopharmacology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c511t-3806441fdb8f6f52cb2fb052f84842f9c56575c4051505ebd610163a2ec1d8f13</citedby><cites>FETCH-LOGICAL-c511t-3806441fdb8f6f52cb2fb052f84842f9c56575c4051505ebd610163a2ec1d8f13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240174/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240174/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27515791$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Decot, Heather K</creatorcontrib><creatorcontrib>Namboodiri, Vijay M K</creatorcontrib><creatorcontrib>Gao, Wei</creatorcontrib><creatorcontrib>McHenry, Jenna A</creatorcontrib><creatorcontrib>Jennings, Joshua H</creatorcontrib><creatorcontrib>Lee, Sung-Ho</creatorcontrib><creatorcontrib>Kantak, Pranish A</creatorcontrib><creatorcontrib>Jill Kao, Yu-Chieh</creatorcontrib><creatorcontrib>Das, Manasmita</creatorcontrib><creatorcontrib>Witten, Ilana B</creatorcontrib><creatorcontrib>Deisseroth, Karl</creatorcontrib><creatorcontrib>Shih, Yen-Yu Ian</creatorcontrib><creatorcontrib>Stuber, Garret D</creatorcontrib><title>Coordination of Brain-Wide Activity Dynamics by Dopaminergic Neurons</title><title>Neuropsychopharmacology (New York, N.Y.)</title><addtitle>Neuropsychopharmacology</addtitle><description>Several neuropsychiatric conditions, such as addiction and schizophrenia, may arise in part from dysregulated activity of ventral tegmental area dopaminergic (TH
) neurons, as well as from more global maladaptation in neurocircuit function. However, whether TH
activity affects large-scale brain-wide function remains unknown. Here we selectively activated TH
neurons in transgenic rats and measured resulting changes in whole-brain activity using stimulus-evoked functional magnetic resonance imaging. Applying a standard generalized linear model analysis approach, our results indicate that selective optogenetic stimulation of TH
neurons enhanced cerebral blood volume signals in striatal target regions in a dopamine receptor-dependent manner. However, brain-wide voxel-based principal component analysis of the same data set revealed that dopaminergic modulation activates several additional anatomically distinct regions throughout the brain, not typically associated with dopamine release events. Furthermore, explicit pairing of TH
neuronal activation with a forepaw stimulus of a particular frequency expanded the sensory representation of that stimulus, not exclusively within the somatosensory cortices, but brain-wide. These data suggest that modulation of TH
neurons can impact brain dynamics across many distributed anatomically distinct regions, even those that receive little to no direct TH
input.</description><subject>Addictions</subject><subject>Animals</subject><subject>Benzazepines - administration & dosage</subject><subject>Benzazepines - pharmacology</subject><subject>Biomedical engineering</subject><subject>Brain - diagnostic imaging</subject><subject>Brain - drug effects</subject><subject>Brain - physiology</subject><subject>Brain research</subject><subject>Cerebrovascular Circulation - drug effects</subject><subject>Cerebrovascular Circulation - physiology</subject><subject>Dopamine</subject><subject>Dopamine - metabolism</subject><subject>Dopaminergic Neurons - physiology</subject><subject>Functional Neuroimaging - methods</subject><subject>Generalized linear models</subject><subject>Magnetic resonance imaging</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Male</subject><subject>Neurosciences</subject><subject>Original</subject><subject>Physiology</subject><subject>Rats</subject><subject>Rats, Long-Evans</subject><subject>Receptors, Dopamine D1 - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Neuropsychopharmacology (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Decot, Heather K</au><au>Namboodiri, Vijay M K</au><au>Gao, Wei</au><au>McHenry, Jenna A</au><au>Jennings, Joshua H</au><au>Lee, Sung-Ho</au><au>Kantak, Pranish A</au><au>Jill Kao, Yu-Chieh</au><au>Das, Manasmita</au><au>Witten, Ilana B</au><au>Deisseroth, Karl</au><au>Shih, Yen-Yu Ian</au><au>Stuber, Garret D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Coordination of Brain-Wide Activity Dynamics by Dopaminergic Neurons</atitle><jtitle>Neuropsychopharmacology (New York, N.Y.)</jtitle><addtitle>Neuropsychopharmacology</addtitle><date>2017-02-01</date><risdate>2017</risdate><volume>42</volume><issue>3</issue><spage>615</spage><epage>627</epage><pages>615-627</pages><issn>0893-133X</issn><eissn>1740-634X</eissn><coden>NEROEW</coden><abstract>Several neuropsychiatric conditions, such as addiction and schizophrenia, may arise in part from dysregulated activity of ventral tegmental area dopaminergic (TH
) neurons, as well as from more global maladaptation in neurocircuit function. However, whether TH
activity affects large-scale brain-wide function remains unknown. Here we selectively activated TH
neurons in transgenic rats and measured resulting changes in whole-brain activity using stimulus-evoked functional magnetic resonance imaging. Applying a standard generalized linear model analysis approach, our results indicate that selective optogenetic stimulation of TH
neurons enhanced cerebral blood volume signals in striatal target regions in a dopamine receptor-dependent manner. However, brain-wide voxel-based principal component analysis of the same data set revealed that dopaminergic modulation activates several additional anatomically distinct regions throughout the brain, not typically associated with dopamine release events. Furthermore, explicit pairing of TH
neuronal activation with a forepaw stimulus of a particular frequency expanded the sensory representation of that stimulus, not exclusively within the somatosensory cortices, but brain-wide. These data suggest that modulation of TH
neurons can impact brain dynamics across many distributed anatomically distinct regions, even those that receive little to no direct TH
input.</abstract><cop>England</cop><pub>Nature Publishing Group</pub><pmid>27515791</pmid><doi>10.1038/npp.2016.151</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Addictions Animals Benzazepines - administration & dosage Benzazepines - pharmacology Biomedical engineering Brain - diagnostic imaging Brain - drug effects Brain - physiology Brain research Cerebrovascular Circulation - drug effects Cerebrovascular Circulation - physiology Dopamine Dopamine - metabolism Dopaminergic Neurons - physiology Functional Neuroimaging - methods Generalized linear models Magnetic resonance imaging Magnetic Resonance Imaging - methods Male Neurosciences Original Physiology Rats Rats, Long-Evans Receptors, Dopamine D1 - antagonists & inhibitors Ventral Tegmental Area - diagnostic imaging Ventral Tegmental Area - drug effects Ventral Tegmental Area - physiology |
title | Coordination of Brain-Wide Activity Dynamics by Dopaminergic Neurons |
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