Literature DB >> 14960596

Dopamine operates as a subsecond modulator of food seeking.

Mitchell F Roitman1, Garret D Stuber, Paul E M Phillips, R Mark Wightman, Regina M Carelli.   

Abstract

The dopamine projection to the nucleus accumbens has been implicated in behaviors directed toward the acquisition and consumption of natural rewards. The neurochemical studies that established this link made time-averaged measurements over minutes, and so the precise temporal relationship between dopamine changes and these behaviors is not known. To resolve this, we sampled dopamine every 100 msec using fast-scan cyclic voltammetry at carbon-fiber microelectrodes in the nucleus accumbens of rats trained to press a lever for sucrose. Cues that signal the opportunity to respond for sucrose evoked dopamine release (67 +/- 20 nm) with short latency (0.2 +/- 0.1 sec onset). When the same cues were presented to rats naive to the cue-sucrose pairing, similar dopamine signals were not observed. Thus, cue-evoked increases in dopamine in trained rats reflected a learned association between the cues and sucrose availability. Lever presses for sucrose occurred at the peak of the dopamine surges. After lever presses, and while sucrose was delivered and consumed, no further increases in dopamine were detected. Rather, dopamine returned to baseline levels. Together, the results strongly implicate subsecond dopamine signaling in the nucleus accumbens as a real-time modulator of food-seeking behavior.

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Year:  2004        PMID: 14960596      PMCID: PMC6730321          DOI: 10.1523/JNEUROSCI.3823-03.2004

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  299 in total

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Authors:  Jeremy J Day; Joshua L Jones; R Mark Wightman; Regina M Carelli
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2.  Extinction learning of rewards in the rat: is there a role for CB1 receptors?

Authors:  Giovanni Hernandez; Joseph F Cheer
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3.  Rapid dopamine signaling differentially modulates distinct microcircuits within the nucleus accumbens during sucrose-directed behavior.

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Journal:  Biol Psychiatry       Date:  2012-02-02       Impact factor: 13.382

5.  Methamphetamine-induced dopamine terminal deficits in the nucleus accumbens are exacerbated by reward-associated cues and attenuated by CB1 receptor antagonism.

Authors:  Gabriel C Loewinger; Michael V Beckert; Hugo A Tejeda; Joseph F Cheer
Journal:  Neuropharmacology       Date:  2012-01-25       Impact factor: 5.250

Review 6.  Establishing causality for dopamine in neural function and behavior with optogenetics.

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Journal:  Brain Res       Date:  2012-09-29       Impact factor: 3.252

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Review 8.  A role for phasic dopamine release within the nucleus accumbens in encoding aversion: a review of the neurochemical literature.

Authors:  Jennifer M Wenzel; Noah A Rauscher; Joseph F Cheer; Erik B Oleson
Journal:  ACS Chem Neurosci       Date:  2014-12-24       Impact factor: 4.418

9.  Dopamine dependency for acquisition and performance of Pavlovian conditioned response.

Authors:  Martin Darvas; Amanda M Wunsch; Jeffrey T Gibbs; Richard D Palmiter
Journal:  Proc Natl Acad Sci U S A       Date:  2014-02-03       Impact factor: 11.205

10.  Transient inactivation of the ventral tegmental area selectively disrupts the expression of conditioned place preference for pup- but not cocaine-paired contexts.

Authors:  Katharine M Seip; Joan I Morrell
Journal:  Behav Neurosci       Date:  2009-12       Impact factor: 1.912

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