A pair of dopamine neurons target the D1-like dopamine receptor DopR in the central complex to promote ethanol-stimulated locomotion in Drosophila
Dopamine is a mediator of the stimulant properties of drugs of abuse, including ethanol, in mammals and in the fruit fly Drosophila. The neural substrates for the stimulant actions of ethanol in flies are not known. We show that a subset of dopamine neurons and their targets, through the action of t...
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Published in | PloS one Vol. 5; no. 4; p. e9954 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Public Library of Science
01.04.2010
Public Library of Science (PLoS) |
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Abstract | Dopamine is a mediator of the stimulant properties of drugs of abuse, including ethanol, in mammals and in the fruit fly Drosophila. The neural substrates for the stimulant actions of ethanol in flies are not known. We show that a subset of dopamine neurons and their targets, through the action of the D1-like dopamine receptor DopR, promote locomotor activation in response to acute ethanol exposure. A bilateral pair of dopaminergic neurons in the fly brain mediates the enhanced locomotor activity induced by ethanol exposure, and promotes locomotion when directly activated. These neurons project to the central complex ellipsoid body, a structure implicated in regulating motor behaviors. Ellipsoid body neurons are required for ethanol-induced locomotor activity and they express DopR. Elimination of DopR blunts the locomotor activating effects of ethanol, and this behavior can be restored by selective expression of DopR in the ellipsoid body. These data tie the activity of defined dopamine neurons to D1-like DopR-expressing neurons to form a neural circuit that governs acute responding to ethanol. |
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AbstractList | Dopamine is a mediator of the stimulant properties of drugs of abuse, including ethanol, in mammals and in the fruit fly Drosophila. The neural substrates for the stimulant actions of ethanol in flies are not known. We show that a subset of dopamine neurons and their targets, through the action of the D1-like dopamine receptor DopR, promote locomotor activation in response to acute ethanol exposure. A bilateral pair of dopaminergic neurons in the fly brain mediates the enhanced locomotor activity induced by ethanol exposure, and promotes locomotion when directly activated. These neurons project to the central complex ellipsoid body, a structure implicated in regulating motor behaviors. Ellipsoid body neurons are required for ethanol-induced locomotor activity and they express DopR. Elimination of DopR blunts the locomotor activating effects of ethanol, and this behavior can be restored by selective expression of DopR in the ellipsoid body. These data tie the activity of defined dopamine neurons to D1-like DopR-expressing neurons to form a neural circuit that governs acute responding to ethanol. Dopamine is a mediator of the stimulant properties of drugs of abuse, including ethanol, in mammals and in the fruit fly Drosophila . The neural substrates for the stimulant actions of ethanol in flies are not known. We show that a subset of dopamine neurons and their targets, through the action of the D1-like dopamine receptor DopR, promote locomotor activation in response to acute ethanol exposure. A bilateral pair of dopaminergic neurons in the fly brain mediates the enhanced locomotor activity induced by ethanol exposure, and promotes locomotion when directly activated. These neurons project to the central complex ellipsoid body, a structure implicated in regulating motor behaviors. Ellipsoid body neurons are required for ethanol-induced locomotor activity and they express DopR. Elimination of DopR blunts the locomotor activating effects of ethanol, and this behavior can be restored by selective expression of DopR in the ellipsoid body. These data tie the activity of defined dopamine neurons to D1-like DopR-expressing neurons to form a neural circuit that governs acute responding to ethanol. |
Audience | Academic |
Author | Lebestky, Tim Heberlein, Ulrike Sniffen, Melissa R Wolf, Fred W Mayer, Nasima Kong, Eric C Hirsh, Jay Li, Haiyan Bainton, Roland J Woo, Katherine |
AuthorAffiliation | UCLA, United States of America 2 Department of Anatomy, University of California San Francisco, San Francisco, California, United States of America 1 Ernest Gallo Clinic and Research Center, Emeryville, California, United States of America 3 Department of Biology, University of Virginia, Charlottesville, Virginia, United States of America 5 Department of Anesthesia, University of California San Francisco, San Francisco, California, United States of America 4 Division of Biology, California Institute of Technology, Pasadena, California, United States of America |
AuthorAffiliation_xml | – name: 1 Ernest Gallo Clinic and Research Center, Emeryville, California, United States of America – name: UCLA, United States of America – name: 3 Department of Biology, University of Virginia, Charlottesville, Virginia, United States of America – name: 4 Division of Biology, California Institute of Technology, Pasadena, California, United States of America – name: 5 Department of Anesthesia, University of California San Francisco, San Francisco, California, United States of America – name: 2 Department of Anatomy, University of California San Francisco, San Francisco, California, United States of America |
Author_xml | – sequence: 1 givenname: Eric C surname: Kong fullname: Kong, Eric C organization: Ernest Gallo Clinic and Research Center, Emeryville, California, United States of America – sequence: 2 givenname: Katherine surname: Woo fullname: Woo, Katherine – sequence: 3 givenname: Haiyan surname: Li fullname: Li, Haiyan – sequence: 4 givenname: Tim surname: Lebestky fullname: Lebestky, Tim – sequence: 5 givenname: Nasima surname: Mayer fullname: Mayer, Nasima – sequence: 6 givenname: Melissa R surname: Sniffen fullname: Sniffen, Melissa R – sequence: 7 givenname: Ulrike surname: Heberlein fullname: Heberlein, Ulrike – sequence: 8 givenname: Roland J surname: Bainton fullname: Bainton, Roland J – sequence: 9 givenname: Jay surname: Hirsh fullname: Hirsh, Jay – sequence: 10 givenname: Fred W surname: Wolf fullname: Wolf, Fred W |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/20376353$$D View this record in MEDLINE/PubMed |
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ContentType | Journal Article |
Copyright | COPYRIGHT 2010 Public Library of Science 2010 Kong et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. Kong et al. 2010 |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Conceived and designed the experiments: ECK KW UH JH FW. Performed the experiments: ECK KW HL NM MRS FW. Analyzed the data: ECK HL RJB FW. Contributed reagents/materials/analysis tools: ECK TL RJB. Wrote the paper: FW. |
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Snippet | Dopamine is a mediator of the stimulant properties of drugs of abuse, including ethanol, in mammals and in the fruit fly Drosophila. The neural substrates for... Dopamine is a mediator of the stimulant properties of drugs of abuse, including ethanol, in mammals and in the fruit fly Drosophila . The neural substrates for... |
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SubjectTerms | Addictions Addictive behaviors Alcoholism Animal behavior Animals Behavior, Animal - drug effects Biology Brain Brain research Central Nervous System Depressants Cloning Cocaine Dopamine Dopamine - physiology Dopamine D1 receptors Dopamine receptors Drosophila Drosophila melanogaster Drosophila Proteins - metabolism Drug abuse Drug dosages Drugs Ethanol Ethanol - pharmacology Exposure Fruit flies (Tephritidae) Gene expression Genetics and Genomics/Disease Models Genetics and Genomics/Genetics of Disease Hyperactivity Insects Locomotion Locomotion - drug effects Locomotor activity Motor Activity Narcotics Nervous system Neural circuitry Neurons Neurons - physiology Neuroscience/Behavioral Neuroscience Phenols (Class of compounds) Receptors, Dopamine - metabolism Rodents Studies Substrates |
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Title | A pair of dopamine neurons target the D1-like dopamine receptor DopR in the central complex to promote ethanol-stimulated locomotion in Drosophila |
URI | https://www.ncbi.nlm.nih.gov/pubmed/20376353 https://www.proquest.com/docview/1289449118 https://search.proquest.com/docview/733864442 https://pubmed.ncbi.nlm.nih.gov/PMC2848596 https://doaj.org/article/066104f738704f84a55f0858b57064bc http://dx.doi.org/10.1371/journal.pone.0009954 |
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