Evidence map›Paper›PMID 30150359›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2018

Granulocyte Colony Stimulating Factor Enhances Reward Learning through Potentiation of Mesolimbic Dopamine System Function.

Munir Gunes Kutlu, Lillian J Brady, Emily G Peck, Rebecca S Hofford, Jordan T Yorgason, Cody A Siciliano, Drew D Kiraly, Erin S Calipari

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

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  12. The role of gut-immune-brain signaling in substance use disorders.International review of neurobiology · 2021
    Article
  13. Where Is Dopamine and how do Immune Cells See it?: Dopamine-Mediated Immune Cell Function in Health and Disease.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2020
    Review
  14. Article
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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

8 authors at 5 institutions in 2 countries.

Munir Gunes KutluDepartment of Pharmacology.
Lillian J BradyDepartment of Pharmacology.
Emily G PeckDepartment of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, North Carolina 07141.
Rebecca S HoffordDepartment of Psychiatry.
Jordan T YorgasonDepartment of Physiology and Developmental Biology, Brigham Young University, Provo, Utah 84602.
Cody A SicilianoDepartment of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, North Carolina 07141.ORCID 0000-0001-9871-2089
Drew D KiralyDepartment of Psychiatry, erin.calipari@vanderbilt.edu drew.kiraly@mssm.edu.
Erin S CalipariDepartment of Pharmacology, erin.calipari@vanderbilt.edu drew.kiraly@mssm.edu.
Institute of Pharmacology · CZWake Forest University · USAllen Institute for Brain Science · USBrigham Young University · USVanderbilt University · US

Funding

Wake Forest Translational Alcohol Research Center (WF-TARC)P50AA026117 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Jeffrey L. Weiner · 2018 to 2026
$16.2M
MULTI-DISCIPLINARY TRAINING IN THE BIOLOGY OF ALCOHOLISMT32AA007565 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI BRIAN A MCCOOL · 1994 to 2026
$10.1M
The Neurobiology of Drug AbuseT32DA041349 · NIDA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI SARA RAULERSON JONES · 2017 to 2026
$1.8M
Dissecting the role of granulocyte-colony stimulating factor in cocaine-mediated behavioral plasticityK08DA044308 · NIDA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KIRALY, DREW · 2017 to 2021
$938k
Defining the Role of D1 and D2 Medium Spiny Neurons in Relapse to Cocaine SeekingR00DA042111 · NIDA · VANDERBILT UNIVERSITY · PI CALIPARI, ERIN · 2018 to 2020
$747k
Defining the Role of D1 and D2 Medium Spiny Neurons in Relapse to Cocaine SeekingK99DA042111 · NIDA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CALIPARI, ERIN · 2016 to 2017
$301k
Elucidating the role of basolateral amygdala projections to the lateral hypothalamus in associative learningF32MH111216 · NIMH · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI SICILIANO, CODY · 2016 to 2017
$103k
NIAAA NIH HHS P50 AA026117NIAAA NIH HHS T32 AA007565NIDA NIH HHS K08 DA044308NIDA NIH HHS K99 DA042111NIDA NIH HHS R00 DA042111NIDA NIH HHS T32 DA041349NIMH NIH HHS F32 MH111216
6 · The paper itself

Abstract

Deficits in motivation and cognition are hallmark symptoms of multiple psychiatric diseases. These symptoms are disruptive to quality of life and often do not improve with available medications. In recent years there has been increased interest in the role of the immune system in neuropsychiatric illness, but to date no immune-related treatment strategies have come to fruition. The cytokine granulocyte-colony stimulating factor (G-CSF) is known to have trophic and neuroprotective properties in the brain, and we recently identified it as a modulator of neuronal and behavioral plasticity. By combining operant tasks that assess discrete aspects of motivated behavior and decision-making in male mice and rats with subsecond dopamine monitoring via fast-scan cyclic voltammetry, we defined the role of G-CSF in these processes as well as the neural mechanism by which it modulates dopamine function to exert these effects. G-CSF enhanced motivation for sucrose as well as cognitive flexibility as measured by reversal learning. These behavioral outcomes were driven by mesolimbic dopamine system plasticity, as systemically administered G-CSF increased evoked dopamine release in the nucleus accumbens independent of clearance mechanisms. Importantly, sustained increases in G-CSF were required for these effects as acute exposure did not enhance behavioral outcomes and decreased dopamine release. These effects seem to be a result of the ability of G-CSF to alter local inflammatory signaling cascades, particularly tumor necrosis factor α. Together, these data show G-CSF as a potent modulator of the mesolimbic dopamine circuit and its ability to appropriately attend to salient stimuli.

Indexed as

RewardAnimalsConditioning, OperantDecision MakingDopamineGranulocyte Colony-Stimulating FactorMaleMice, Inbred C57BLMotivationNucleus AccumbensRats, Sprague-DawleyReversal LearningSucroseDopamineGranulocyte Colony-Stimulating FactorSucrosecytokinedopamineimmune systemlearning and memorymotivationvoltammetry

Identifiers

PMID30150359
PMCPMC6181308
OpenAlexW2888916042

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.