Evidence map›Paper›PMID 26192746›Full record

ArticleNature neuroscience2015

The role of ventral striatal cAMP signaling in stress-induced behaviors.

Florian Plattner, Kanehiro Hayashi, Adan Hernández, David R Benavides, Tara C Tassin, Chunfeng Tan, Jonathan Day, Maggy W Fina, Eunice Y Yuen, Zhen Yan and 8 more

Abstract read
In one paragraph

Article in Nature neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

47 citing papers in PubMed, 92 citations in OpenAlex.

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  9. Reversing anxiety by targeting a stress-responsive signaling pathway.Proceedings of the National Academy of Sciences of the United States of America · 2024
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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

18 authors at 9 institutions in 3 countries.

Florian PlattnerDepartment of Psychiatry, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Kanehiro HayashiDepartment of Psychiatry, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Adan HernándezDepartment of Psychiatry, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
David R BenavidesDepartment of Psychiatry, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Tara C TassinDepartment of Psychiatry, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Chunfeng TanDepartment of Psychiatry, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Jonathan DayDivision of Neuroscience and Molecular Pharmacology, Institute of Biomedical and Life Sciences, University of Glasgow, Glasgow, UK.
Maggy W FinaDepartment of Pharmacology, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Eunice Y YuenDepartment of Physiology and Biophysics, State University of New York at Buffalo, Buffalo, New York, USA.
Zhen YanDepartment of Physiology and Biophysics, State University of New York at Buffalo, Buffalo, New York, USA.
Matthew S Goldberg1] Department of Psychiatry, The University of Texas Southwestern Medical Center, Dallas, Texas, USA. [2] Department of Neurology and Neurotherapeutics, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Angus C Nairn1] Department of Psychiatry, Yale University School of Medicine, New Haven, Connecticut, USA. [2] Laboratory of Molecular and Cellular Neuroscience, The Rockefeller University, New York, New York, USA.
Paul GreengardLaboratory of Molecular and Cellular Neuroscience, The Rockefeller University, New York, New York, USA.
Eric J NestlerFishberg Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Ronald TaussigDepartment of Pharmacology, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Akinori NishiDepartment of Pharmacology, Kurume University School of Medicine, Fukuoka, Japan.
Miles D HouslayInstitute of Pharmaceutical Science, King's College London, London, UK.
James A Bibb1] Department of Psychiatry, The University of Texas Southwestern Medical Center, Dallas, Texas, USA. [2] Department of Neurology and Neurotherapeutics, The University of Texas Southwestern Medical Center, Dallas, Texas, USA. [3] Harold C. Simmons Comprehensive Cancer Center, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
The University of Texas Southwestern Medical Center · USRockefeller University · USAllen Institute for Brain Science · USBuffalo State University · USKeio University · JPKing's College London · GBKurume University · JPUniversity at Buffalo, State University of New York · USUniversity of Glasgow · GB

Funding

Yale/NIDA Neuroproteomics Research CenterP30DA018343 · NIDA · YALE UNIVERSITY · PI ANGUS C. NAIRN, Kenneth Robert WILLIAMS · 2004 to 2026
$37.1M
THE ROLE OF DARPPS IN THE ACUTE AND CHRONIC EFFECTS OF COCAINE AND AMPHETAMINEP01DA010044 · NIDA · ROCKEFELLER UNIVERSITY · PI GREENGARD, PAUL · 1996 to 2015
$23.6M
REPRESSIVE HISTONE AND DNA METHYLATION IN RODENT DEPRESSION MODELSP50MH096890 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ALLIS, CHARLES DAVID · 2012 to 2021
$20.2M
Using neuroeconomics to disentangle the transcriptional mechanisms underlying resilience versus susceptibility to stressR01MH051399 · NIMH · YALE UNIVERSITY · PI NESTLER, ERIC J. · 1994 to 2023
$10.2M
Striatal Cell-specific Analysis of the Molecular Mechanisms of Antipsychotic DrugP50MH090963 · NIMH · ROCKEFELLER UNIVERSITY · PI FLAJOLET, MARC · 2010 to 2014
$9.8M
REGION-SPECIFIC PHOSPHOPROTEINS IN THE BASAL GANGLIAP01MH040899 · NIMH · ROCKEFELLER UNIVERSITY · PI GREENGARD, PAUL · 1985 to 2004
$7.0M
The Role of Cdk5 in AddictionR01DA016672 · NIDA · UT SOUTHWESTERN MEDICAL CENTER · PI BIBB, JAMES A · 2003 to 2010
$2.5M
Physiological and Pathophysiological Basis of StressR01MH108842 · NIMH · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI YAN, ZHEN · 2015 to 2019
$2.0M
Novel Signal Transduction Mechanisms in Learning and MemoryR01MH083711 · NIMH · UT SOUTHWESTERN MEDICAL CENTER · PI BIBB, JAMES A · 2010 to 2014
$2.0M
The Role of Cdk5 in StrokeR01NS073855 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI BIBB, JAMES A · 2012 to 2017
$1.7M
Functions of D4 Dopamine Receptors in Prefrontal CortexR01DA037618 · NIDA · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI YAN, ZHEN · 2014 to 2018
$1.7M
The Regulation of Dopamine Neurotransmission by CDK5R01MH079710 · NIMH · UT SOUTHWESTERN MEDICAL CENTER · PI BIBB, JAMES A · 2008 to 2011
$1.7M
NIDA NIH HHS DA016672NIDA NIH HHS DA018343NIDA NIH HHS DA033485NIDA NIH HHS DA10044NIDA NIH HHS P01 DA010044NIDA NIH HHS P30 DA018343NIDA NIH HHS R01 DA016672NIDA NIH HHS R01 DA033485NIDA NIH HHS R01 DA037618NIGMS NIH HHS GM084249NIGMS NIH HHS R01 GM084249NIMH NIH HHS MH083711NIMH NIH HHS MH090963NIMH NIH HHS MH51399NIMH NIH HHS MH79710NIMH NIH HHS P01 MH040899NIMH NIH HHS P50 MH090963NIMH NIH HHS P50 MH096890NIMH NIH HHS R01 MH051399NIMH NIH HHS R01 MH079710NIMH NIH HHS R01 MH083711NIMH NIH HHS R01 MH108842NINDS NIH HHS F32 NS010161NINDS NIH HHS NS073855NINDS NIH HHS R01 NS073855
6 · The paper itself

Abstract

The cAMP and cAMP-dependent protein kinase A (PKA) signaling cascade is a ubiquitous pathway acting downstream of multiple neuromodulators. We found that the phosphorylation of phosphodiesterase-4 (PDE4) by cyclin-dependent protein kinase 5 (Cdk5) facilitated cAMP degradation and homeostasis of cAMP/PKA signaling. In mice, loss of Cdk5 throughout the forebrain elevated cAMP levels and increased PKA activity in striatal neurons, and altered behavioral responses to acute or chronic stressors. Ventral striatum- or D1 dopamine receptor-specific conditional knockout of Cdk5, or ventral striatum infusion of a small interfering peptide that selectively targeted the regulation of PDE4 by Cdk5, produced analogous effects on stress-induced behavioral responses. Together, our results demonstrate that altering cAMP signaling in medium spiny neurons of the ventral striatum can effectively modulate stress-induced behavioral states. We propose that targeting the Cdk5 regulation of PDE4 could be a new therapeutic approach for clinical conditions associated with stress, such as depression.

Indexed as

AnimalsBehavior, AnimalCyclic AMPCyclic AMP-Dependent Protein KinasesCyclic Nucleotide Phosphodiesterases, Type 4Cyclin-Dependent Kinase 5MaleMiceMice, Inbred C57BLMice, KnockoutSignal TransductionStress, PsychologicalVentral StriatumCdk5 protein, mouseCyclic AMPCyclic AMP-Dependent Protein KinasesCyclic Nucleotide Phosphodiesterases, Type 4Cyclin-Dependent Kinase 5

Identifiers

PMID26192746
PMCPMC4519694
OpenAlexW1913344680

What OpenQuestion holds

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Registered trials

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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.