Behavioral dopamine signals.

By Wolfram Schultz. Trends in Neurosciences, 2007

1,034 citations recorded by the source corpus.

Subfields: Cellular and Molecular Neuroscience, Cognitive Neuroscience

View Paper: https://www.semanticscholar.org/paper/b11599a376389e105d111336c22d342250992b3e

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In Cellular and Molecular Neuroscience

In Cognitive Neuroscience

Citations in the corpus

Worth the ‘EEfRT’? The Effort Expenditure for Rewards Task as an Objective Measure of Motivation and Anhedonia (2009, background): “been shown to influence Nacc DA release during reward anticipation [47].”
Reward Processing by the Opioid System in the Brain (2009, critical): “Nonetheless, accumulating experimental evidence argues against dopamine (DA) mediation of reward processes per se (37, 58, 112, 326, 333, 412).”
FOXP2 as a molecular window into speech and language. (2009, background): “In mammals, nigral dopamine acts on various behavioural systems, including reward learning [ 67 ].”
Eight Different Types of Dopaminergic Neurons Innervate the Drosophila Mushroom Body Neuropil: Anatomical and Physiological Heterogeneity (2009, neutral): “Aversive events produce depressions of DA neuron activity (Schultz, 2007).”
A common neurobiology for pain and pleasure (2008, background): “Dopamine, motivation and analgesia Considering the close association that exists between motivation, learning and hedonic feelings, it is not surprising that dopamine signalling has been consistently reported to correlate with stimulus reward valu”
Synaptic Consolidation: From Synapses to Behavioral Modeling (2015, background): “A phasic increase in dopamine in turn can be caused by behavioral and environmental cues such as novelty, reward prediction error, aversive events,or attention (Ljunberg et al., 1992; Hollerman and Schultz, 1998; Redgrave and Gurney, 2006; Schultz, 2007; Bethus et al., 2010; Lisman et al., 2011).”
Unique properties of mesoprefrontal neurons within a dual mesocorticolimbic dopamine system. (2008, positive): “Thus, based on the combination of our functional and molecular data, the fast-firing mesocorticolimbic DA neurons with a low dopamine reuptake capacity appear well suited to mediate the often sustained forms of behaviorally relevant DA release in vivo in several brain regions (Bassareo et al., 2002;”
What is reinforcement sensitivity? Neuroscience paradigms for approach‐avoidance process theories of personality (2008, background): “Phasic activity of DA neurons increases in response to unpredicted reward, decreases in response to unpredicted non-reward, and is sustained when rewards are fully predicted (Day, Roitman,Wightman, & Carelli, 2007; Pickering & Smillie, 2008; Schultz, 1998, 2007).”
Striatal plasticity and basal ganglia circuit function (2008, background): “In the striatum, the primary instructive signal for learning is thought to be dopamine release, which, according to one prominent theory, can signal a ‘‘reward prediction error’’ (Montague et al., 2004; Schultz, 2007).”
Functional Requirements for Reward-Modulated Spike-Timing-Dependent Plasticity (2010, background): “This is because, as we have shown in this paper, R-STDP needs an RPE system, but before the critic is trained the RPEs are not available.”
Dopaminergic reward system: a short integrative review (2010, background): “These results are derived from selective lesions of different components of DA systems, systemic and intracerebral administration of direct and indirect DA receptor agonist and antagonist drugs, electrical self-stimulation, and selfadministration of major drugs of abuse, such as cocaine, amphetamine”
Projection-specific modulation of dopamine neuron synapses by aversive and rewarding stimuli (2011, neutral): “These findings led to the influential hypothesis that phasic DA cell activity encodes a reward prediction error, which is critical for reinforcement-dependent learning (Schultz, 1998, 2007, 2010; D'Ardenne et al., 2008; Dayan and Niv, 2008).”