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Local and Global Consequences of Reward-evoked Striatal Dopamine Release

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Journal Nature
Specialty Science
Date 2020 Apr 10
PMID 32269346
Citations 34
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Abstract

The neurotransmitter dopamine is required for the reinforcement of actions by rewarding stimuli. Neuroscientists have tried to define the functions of dopamine in concise conceptual terms, but the practical implications of dopamine release depend on its diverse brain-wide consequences. Although molecular and cellular effects of dopaminergic signalling have been extensively studied, the effects of dopamine on larger-scale neural activity profiles are less well-understood. Here we combine dynamic dopamine-sensitive molecular imaging and functional magnetic resonance imaging to determine how striatal dopamine release shapes local and global responses to rewarding stimulation in rat brains. We find that dopamine consistently alters the duration, but not the magnitude, of stimulus responses across much of the striatum, via quantifiable postsynaptic effects that vary across subregions. Striatal dopamine release also potentiates a network of distal responses, which we delineate using neurochemically dependent functional connectivity analyses. Hot spots of dopaminergic drive notably include cortical regions that are associated with both limbic and motor function. Our results reveal distinct neuromodulatory actions of striatal dopamine that extend well beyond its sites of peak release, and that result in enhanced activation of remote neural populations necessary for the performance of motivated actions. Our findings also suggest brain-wide biomarkers of dopaminergic function and could provide a basis for the improved interpretation of neuroimaging results that are relevant to learning and addiction.

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References
1.
Wise R . Dopamine, learning and motivation. Nat Rev Neurosci. 2004; 5(6):483-94. DOI: 10.1038/nrn1406. View

2.
Berke J . What does dopamine mean?. Nat Neurosci. 2018; 21(6):787-793. PMC: 6358212. DOI: 10.1038/s41593-018-0152-y. View

3.
Bamford N, Wightman R, Sulzer D . Dopamine's Effects on Corticostriatal Synapses during Reward-Based Behaviors. Neuron. 2018; 97(3):494-510. PMC: 5808590. DOI: 10.1016/j.neuron.2018.01.006. View

4.
Lee T, Cai L, Lelyveld V, Hai A, Jasanoff A . Molecular-level functional magnetic resonance imaging of dopaminergic signaling. Science. 2014; 344(6183):533-5. PMC: 9972887. DOI: 10.1126/science.1249380. View

5.
Olds J, Milner P . Positive reinforcement produced by electrical stimulation of septal area and other regions of rat brain. J Comp Physiol Psychol. 1954; 47(6):419-27. DOI: 10.1037/h0058775. View