TY - JOUR
T1 - Ectopic g-protein expression in dopamine and serotonin neurons blocks cocaine sensitization in Drosophila melanogaster
AU - Li, H.
AU - Chaney, S.
AU - Forte, M.
AU - Hirsh, J.
N1 - Funding Information:
This work was supported by NIH grant GM/DA 27318. We thank Doug Taylor for assistance with the statistical analyses, Cahir O'Kane for generously providing the UAS–TNT fly stocks, and Ulrike Heberlein for communicating results prior to publication.
PY - 2000/2/1
Y1 - 2000/2/1
N2 - Sensitization to repeated doses of psychostimulants is thought to be an important component underlying the addictive process in humans [1-4]. In all vertebrate animal models, including humans [5], and even in fruit flies, sensitization is observed after repeated exposure to volatilized crack cocaine [6]. In vertebrates, sensitization is thought to be initiated by processes occurring in brain regions that contain dopamine cell bodies [2,7]. Here, we show that modulated cell signaling in the Drosophila dopamine and serotonin neurons plays an essential role in cocaine sensitization. Targeted expression of either a stimulatory (Gα(s)) or inhibitory (Gα(i)) G(α) subunit, or tetanus toxin light chain (TNT) in dopamine and serotonin neurons of living flies blocked behavioral sensitization to repeated cocaine exposures. These flies showed alterations in their initial cocaine responsiveness that correlated with compensatory adaptations of postsynaptic receptor sensitivity. Finally, repeated drug stimulation of a nerve cord preparation that is postsynaptic to the brain amine cells failed to induce sensitization, further showing the importance of presynaptic modulation in sensitization.
AB - Sensitization to repeated doses of psychostimulants is thought to be an important component underlying the addictive process in humans [1-4]. In all vertebrate animal models, including humans [5], and even in fruit flies, sensitization is observed after repeated exposure to volatilized crack cocaine [6]. In vertebrates, sensitization is thought to be initiated by processes occurring in brain regions that contain dopamine cell bodies [2,7]. Here, we show that modulated cell signaling in the Drosophila dopamine and serotonin neurons plays an essential role in cocaine sensitization. Targeted expression of either a stimulatory (Gα(s)) or inhibitory (Gα(i)) G(α) subunit, or tetanus toxin light chain (TNT) in dopamine and serotonin neurons of living flies blocked behavioral sensitization to repeated cocaine exposures. These flies showed alterations in their initial cocaine responsiveness that correlated with compensatory adaptations of postsynaptic receptor sensitivity. Finally, repeated drug stimulation of a nerve cord preparation that is postsynaptic to the brain amine cells failed to induce sensitization, further showing the importance of presynaptic modulation in sensitization.
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U2 - 10.1016/S0960-9822(00)00340-7
DO - 10.1016/S0960-9822(00)00340-7
M3 - Article
C2 - 10704417
AN - SCOPUS:0034708147
SN - 0960-9822
VL - 10
SP - 211
EP - 214
JO - Current Biology
JF - Current Biology
IS - 4
ER -