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A pair of dopamine neurons target the D1-like dopamine receptor DopR in the central complex to promote ethanol-stimulated locomotion in Drosophila

Authors :
Katherine Woo
Nasima Mayer
Melissa R. Sniffen
Eric C. Kong
Ulrike Heberlein
Jay Hirsh
Haiyan Li
Fred W. Wolf
Tim Lebestky
Roland J. Bainton
Frye, Mark A
Source :
PLoS ONE, Vol 5, Iss 4, p e9954 (2010), PLoS ONE, PloS one, vol 5, iss 4, Kong, EC; Woo, K; Li, H; Lebestky, T; Mayer, N; Sniffen, MR; et al.(2010). A pair of dopamine neurons target the D1-like dopamine receptor dopr in the central complex to promote ethanol-stimulated locomotion in drosophila. PLoS ONE, 5(4). doi: 10.1371/journal.pone.0009954. UC Merced: Retrieved from: http://www.escholarship.org/uc/item/4sm069xs
Publication Year :
2010
Publisher :
Public Library of Science (PLoS), 2010.

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. © 2010 Kong et al.

Details

Language :
English
ISSN :
19326203
Volume :
5
Issue :
4
Database :
OpenAIRE
Journal :
PLoS ONE
Accession number :
edsair.doi.dedup.....a7eb1e0a04c562200417031ff20fef5c
Full Text :
https://doi.org/10.1371/journal.pone.0009954.