Evidence map›Paper›PMID 34103400›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2021

Selective filtering of excitatory inputs to nucleus accumbens by dopamine and serotonin.

Daniel J Christoffel, Jessica J Walsh, Paul Hoerbelt, Boris D Heifets, Pierre Llorach, Ricardo C Lopez, Charu Ramakrishnan, Karl Deisseroth, Robert C Malenka

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.1field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

40 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Divergent Roles of Nucleus Accumbens D1- and D2-MSNs in Regulating Hedonic Feeding.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  5. Article
  6. Impact of early social isolation on social circuits and behavior: relevance to schizophrenia.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Review
  7. Article
  8. Serotonin modulates nucleus accumbens circuits to suppress aggression.bioRxiv : the preprint server for biology · 2025
    Article
  9. Article
  10. Serotonin and psilocybin activate 5-HTNature communications · 2025
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Specializations in Amygdalar and Hippocampal Innervation of the Primate Nucleus Accumbens Shell.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  17. Article
  18. Review
  19. Article
  20. Striatal Serotonin Release Signals Reward Value.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Daniel J ChristoffelNancy Pritzker Laboratory, Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA 94305.ORCID 0000-0002-6303-5134
Jessica J WalshNancy Pritzker Laboratory, Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA 94305.ORCID 0000-0001-8466-8451
Paul HoerbeltNancy Pritzker Laboratory, Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA 94305.ORCID 0000-0002-8707-5376
Boris D HeifetsNancy Pritzker Laboratory, Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA 94305.
Pierre LlorachDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University School of Medicine, Stanford, CA 94305.
Ricardo C LopezNancy Pritzker Laboratory, Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA 94305.ORCID 0000-0002-1136-9511
Charu RamakrishnanDepartment of Bioengineering, Stanford University, Stanford, CA 94305.
Karl DeisserothDepartment of Bioengineering, Stanford University, Stanford, CA 94305.
Robert C MalenkaNancy Pritzker Laboratory, Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA 94305; malenka@stanford.edu.ORCID 0000-0002-5428-5211
Stanford University · US

Funding

Training CoreP50DA042012 · NIDA · STANFORD UNIVERSITY · PI Karl A. Deisseroth · 2017 to 2026
$27.1M
Interdisciplinary Research Training in Pain and Substance Use DisordersT32DA035165 · NIDA · STANFORD UNIVERSITY · PI SEAN C MACKEY · 2013 to 2026
$7.2M
Neural circuitry and synaptic physiology underlying MDMA's prosocial effectK08MH110610 · NIMH · STANFORD UNIVERSITY · PI HEIFETS, BORIS DOV · 2017 to 2020
$780k
Role of Nucleus Accumbens and Its Glutamatergic Inputs in High-Fat intakeR00DK115895 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CHRISTOFFEL, DANIEL JOSEPH · 2021 to 2023
$736k
Elucidating the Function of Inhibitory Brain Circuits Involved in AnxietyF32MH115668 · NIMH · STANFORD UNIVERSITY · PI HOERBELT, PAUL · 2017 to 2020
$190k
Role of Nucleus Accumbens and Its Glutamatergic Inputs in High-Fat intakeK99DK115895 · NIDDK · STANFORD UNIVERSITY · PI CHRISTOFFEL, DANIEL JOSEPH · 2018 to 2019
$182k
NIDA NIH HHS P50 DA042012NIDA NIH HHS T32 DA035165NIDDK NIH HHS K99 DK115895NIDDK NIH HHS R00 DK115895NIMH NIH HHS F32 MH115668NIMH NIH HHS K08 MH110610
6 · The paper itself

Abstract

The detailed mechanisms by which dopamine (DA) and serotonin (5-HT) act in the nucleus accumbens (NAc) to influence motivated behaviors in distinct ways remain largely unknown. Here, we examined whether DA and 5-HT selectively modulate excitatory synaptic transmission in NAc medium spiny neurons in an input-specific manner. DA reduced excitatory postsynaptic currents (EPSCs) generated by paraventricular thalamus (PVT) inputs but not by ventral hippocampus (vHip), basolateral amygdala (BLA), or medial prefrontal cortex (mPFC) inputs. In contrast, 5-HT reduced EPSCs generated by inputs from all areas except the mPFC. Release of endogenous DA and 5-HT by methamphetamine (METH) and (±)3,4-methylenedioxymethamphetamine (MDMA), respectively, recapitulated these input-specific synaptic effects. Optogenetic inhibition of PVT inputs enhanced cocaine-conditioned place preference, whereas mPFC input inhibition reduced the enhancement of sociability elicited by MDMA. These findings suggest that the distinct, input-specific filtering of excitatory inputs in the NAc by DA and 5-HT contribute to their discrete behavioral effects.

Indexed as

Excitatory Postsynaptic PotentialsAnimalsBehavior, AnimalDopamineMethamphetamineMiceMice, Inbred C57BLNeuronsN-Methyl-3,4-methylenedioxyamphetamineNucleus AccumbensSerotoninSocial InteractionSynaptic TransmissionDopamineMethamphetamineN-Methyl-3,4-methylenedioxyamphetamineSerotonindopamineneuromodulatorsnucleus accumbensrewardserotonin

Identifiers

PMID34103400
PMCPMC8214692
OpenAlexW3171015631

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.