Evidence map›Paper›PMID 33530478›Full record

ArticleCells2021

Regulation of CREB Phosphorylation in Nucleus Accumbens after Relief Conditioning.

Elaheh Soleimanpour, Jorge R Bergado Acosta, Peter Landgraf, Dana Mayer, Evelyn Dankert, Daniela C Dieterich, Markus Fendt

Open access · goldAbstract read
In one paragraph

Article in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 45% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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

7 authors at 2 institutions in 1 country.

Elaheh SoleimanpourInstitute for Pharmacology and Toxicology, Medical Faculty, Otto-von-Guericke University Magdeburg, 39120 Magdeburg, Germany.
Jorge R Bergado AcostaInstitute for Pharmacology and Toxicology, Medical Faculty, Otto-von-Guericke University Magdeburg, 39120 Magdeburg, Germany.
Peter LandgrafInstitute for Pharmacology and Toxicology, Medical Faculty, Otto-von-Guericke University Magdeburg, 39120 Magdeburg, Germany.
Dana MayerInstitute for Pharmacology and Toxicology, Medical Faculty, Otto-von-Guericke University Magdeburg, 39120 Magdeburg, Germany.
Evelyn DankertInstitute for Pharmacology and Toxicology, Medical Faculty, Otto-von-Guericke University Magdeburg, 39120 Magdeburg, Germany.
Daniela C DieterichInstitute for Pharmacology and Toxicology, Medical Faculty, Otto-von-Guericke University Magdeburg, 39120 Magdeburg, Germany.
Markus FendtInstitute for Pharmacology and Toxicology, Medical Faculty, Otto-von-Guericke University Magdeburg, 39120 Magdeburg, Germany.ORCID 0000-0002-3451-1226
Otto-von-Guericke-Universität Magdeburg · DECenter for Behavioral Brain Sciences · DE

Funding

Deutsche Forschungsgemeinschaft SFB779
6 · The paper itself

Abstract

Relief learning is the association of environmental cues with the cessation of aversive events. While there is increasing knowledge about the neural circuitry mediating relief learning, the respective molecular pathways are not known. Therefore, the aim of the present study was to examine different putative molecular pathways underlying relief learning. To this purpose, male rats were subjected either to relief conditioning or to a pseudo conditioning procedure. Forty-five minutes or 6 h after conditioning, samples of five different brain regions, namely the prefrontal cortex, nucleus accumbens (NAC), dorsal striatum, dorsal hippocampus, and amygdala, were collected. Using quantitative Western blots, the expression level of CREB, pCREB, ERK1/2, pERK1/2, CaMKIIα, MAP2K, PKA, pPKA, Akt, pAkt, DARPP-32, pDARPP-32, 14-3-3, and neuroligin2 were studied. Our analyses revealed that relief conditioned rats had higher CREB phosphorylation in NAC 6 h after conditioning than pseudo conditioned rats. The data further revealed that this CREB phosphorylation was mainly induced by dopamine D1 receptor-mediated activation of PKA, however, other kinases, downstream of the NMDA receptor, may also contribute. Taken together, the present study suggests that CREB phosphorylation, induced by a combination of different molecular pathways downstream of dopamine D1 and NMDA receptors, is essential for the acquisition and consolidation of relief learning.

Indexed as

Conditioning, Classical14-3-3 ProteinsAnimalsBehavior, AnimalCalcium-Calmodulin-Dependent Protein Kinase Type 2Cell Adhesion Molecules, NeuronalCyclic AMP-Dependent Protein KinasesCyclic AMP Response Element-Binding ProteinDopamine and cAMP-Regulated Phosphoprotein 32Enzyme ActivationExtracellular Signal-Regulated MAP KinasesMaleMAP Kinase Kinase 1Nerve Tissue ProteinsNucleus AccumbensOrgan Specificity14-3-3 ProteinsCalcium-Calmodulin-Dependent Protein Kinase Type 2Cell Adhesion Molecules, NeuronalCyclic AMP-Dependent Protein KinasesCyclic AMP Response Element-Binding ProteinDopamine and cAMP-Regulated Phosphoprotein 32Extracellular Signal-Regulated MAP KinasesMAP Kinase Kinase 1Nerve Tissue Proteinsneuroligin 2Proto-Oncogene Proteins c-aktReceptors, Dopamine D1Receptors, N-Methyl-D-AspartateCREBnucleus accumbensrelief learningWestern blot

Identifiers

PMID33530478
PMCPMC7912172
OpenAlexW3124803704

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.