Cited by 221Neurotransmitter Receptor Influence on BehaviorNeural and Behavioral Psychology StudiesNeuropeptides and Animal Physiology

The DOI matches its Crossref record; 81 of the 81 references it cites were found in a registry or an index.

Dopamine or opioid stimulation of nucleus accumbens similarly amplify cue‐triggered ‘wanting’ for reward: entire core and medial shell mapped as substrates for PIT enhancement

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Peciña, Susana, Berridge, Kent C.·2013·European Journal of Neuroscience

Abstract

Pavlovian cues [conditioned stimulus (CS+)] often trigger intense motivation to pursue and consume related reward [unconditioned stimulus (UCS)]. But cues do not always trigger the same intensity of motivation. Encountering a reward cue can be more tempting on some occasions than on others. What makes the same cue trigger more intense motivation to pursue reward on a particular encounter? The answer may be the level of incentive salience (‘wanting’) that is dynamically generated by mesocorticolimbic brain systems, influenced especially by dopamine and opioid neurotransmission in the nucleus accumbens (NA c) at that moment. We tested the ability of dopamine stimulation (by amphetamine microinjection) vs. mu opioid stimulation [by d‐Ala, nMe‐Phe, Glyol‐enkephalin (DAMGO) microinjection] of either the core or shell of the NA c to amplify cue‐triggered levels of motivation to pursue sucrose reward, measured with a Pavlovian‐Instrumental Transfer (PIT) procedure, a relatively pure assay of incentive salience. Cue‐triggered ‘wanting’ in PIT was enhanced by amphetamine or DAMGO microinjections equally, and also equally at nearly all sites throughout the entire core and medial shell (except for a small far‐rostral strip of shell). NA c dopamine/opioid stimulations specifically enhanced CS+ ability to trigger phasic peaks of ‘wanting’ to obtain UCS, without altering baseline efforts when CS+ was absent. We conclude that dopamine/opioid stimulation throughout nearly the entire NA c can causally amplify the reactivity of mesocorticolimbic circuits, and so magnify incentive salience or phasic UCS ‘wanting’ peaks triggered by a CS+. Mesolimbic amplification of incentive salience may explain why a particular cue encounter can become irresistibly tempting, even when previous encounters were successfully resisted before.

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Metadata

Authors
Peciña, S., & Berridge, K. C.
Affiliations
  • University of Michigan–Dearborn (US)
  • University of Michigan (US)
Corresponding author
Peciña, Susana
Venue
European Journal of Neuroscience
Publisher
Wiley
Published
2013-03-17
Volume
37
Issue
9
Pages
1529-1540
ISSN
  • 0953-816X (ISSN-L)
  • 1460-9568
OpenAlex
W2164647828
Cited by
216
References
81
Citations by year
2026: 6 · 2025: 7 · 2024: 9 · 2023: 9 · 2022: 14 · 2021: 12 · 2020: 58 · 2019: 20 · 2018: 21 · 2017: 6 · 2016: 14 · 2015: 20 · 2014: 16 · 2013: 3
FWCI
8.67
Type
journal article
Language
en
Open access
Locations
  • European Journal of Neuroscience (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
  • Deep Blue (University of Michigan) (submittedVersion)
Funders
  • National Institutes of Health
  • National Institute of Mental Health (MH-63649, R01MH063649)
  • National Institute on Drug Abuse (DA015188, R01DA015188)
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
Keywords
incentive salience, nucleus accumbens, dopamine, amphetamine, DAMGO, Pavlovian-to-instrumental transfer, conditioned stimulus, mesocorticolimbic circuit, nucleus accumbens shell, nucleus accumbens core, sucrose reward, motivation
MeSH terms
Amphetamine, Animals, Brain Mapping, Conditioning, Classical, Cues, Male, Motivation, Nucleus Accumbens, Reward, Dopamine Agents, Rats, Sprague-Dawley, Enkephalin, Ala(2)-MePhe(4)-Gly(5)-, Rats

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