Evidence map›Paper›PMID 29197324›Full record

ArticleBMC neuroscience2017

Altered phosphorylation, electrophysiology, and behavior on attenuation of PDE4B action in hippocampus.

Susan L Campbell, Thomas van Groen, Inga Kadish, Lisa High Mitchell Smoot, Graeme B Bolger

Open access · goldAbstract read
In one paragraph

Article in BMC neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

19 citing papers in PubMed, 35 citations in OpenAlex.

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  11. What is obesity? : Obesity Musings.International journal of obesity (2005) · 2022
    Article
  12. RORγt-Expressing Pathogenic CD4Journal of immunology (Baltimore, Md. : 1950) · 2022
    Article
  13. Review
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  15. Article
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  17. Latent Sex Differences in Molecular Signaling That Underlies Excitatory Synaptic Potentiation in the Hippocampus.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  18. Review
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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

5 authors at 2 institutions in 1 country.

Susan L CampbellDepartment of Neurobiology, University of Alabama at Birmingham, Birmingham, AL, 35294, USA.
Thomas van GroenDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, AL, 35294, USA.
Inga KadishDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, AL, 35294, USA.
Lisa High Mitchell SmootDepartment of Medicine, University of Alabama at Birmingham, NP 2501, 1720 2nd Ave S, Birmingham, AL, 35294-3300, USA.
Graeme B BolgerDepartment of Pharmacology, University of Alabama at Birmingham, Birmingham, AL, 35294, USA. gbbolger@uab.edu.
University of Alabama at Birmingham · USCarilion Clinic · US

Funding

XRAY CRYSTALLOGRAPHYP30CA013148 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Robert S Welner · 1985 to 2026
$165.9M
National Cancer Institute P30 CA013148NCI NIH HHS P30 CA013148
6 · The paper itself

Abstract

backgroundPDE4 cyclic nucleotide phosphodiesterases regulate 3', 5' cAMP abundance in the CNS and thereby regulate PKA activity and phosphorylation of CREB, which has been implicated in learning and memory, depression and other functions. The PDE4 isoform PDE4B1 also interacts with the DISC1 protein, implicated in neural development and behavioral disorders. The cellular functions of PDE4B1 have been investigated extensively, but its function(s) in the intact organism remained unexplored.

resultsTo specifically disrupt PDE4B1, we developed mice that express a PDE4B1-D564A transgene in the hippocampus and forebrain. The transgenic mice showed enhanced phosphorylation of CREB and ERK1/2 in hippocampus. Hippocampal neurogenesis was increased in the transgenic mice. Hippocampal electrophysiological studies showed increased baseline synaptic transmission and enhanced LTP in male transgenic mice. Behaviorally, male transgenic mice showed increased activity in prolonged open field testing, but neither male nor female transgenic mice showed detectable anxiety-like behavior or antidepressant effects in the elevated plus-maze, tail-suspension or forced-swim tests. Neither sex showed any significant differences in associative fear conditioning or showed any demonstrable abnormalities in pre-pulse inhibition.

conclusionsThese data support the use of an isoform-selective approach to the study of PDE4B1 function in the CNS and suggest a probable role of PDE4B1 in synaptic plasticity and behavior. They also provide additional rationale and a refined approach to the development of small-molecule PDE4B1-selective inhibitors, which have potential functions in disorders of cognition, memory, mood and affect.

Indexed as

AnimalsAnxietyAssociation LearningConditioning, PsychologicalCyclic AMP Response Element-Binding ProteinCyclic Nucleotide Phosphodiesterases, Type 4DepressionFearFemaleHippocampusIsoenzymesLong-Term PotentiationMaleMemoryMice, TransgenicMitogen-Activated Protein Kinase 1Creb1 protein, mouseCyclic AMP Response Element-Binding ProteinCyclic Nucleotide Phosphodiesterases, Type 4IsoenzymesMapk1 protein, mouseMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3PDE4B protein, mouseCREBDepressionDISC1LearningMemoryPDE4PDE4B1PKA

Identifiers

PMID29197324
PMCPMC5712142
OpenAlexW2775550557

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.