Evidence map›Paper›PMID 28337525›Full record

ArticlePsychopharmacology2017

Phosphodiesterase-1b (Pde1b) knockout mice are resistant to forced swim and tail suspension induced immobility and show upregulation of Pde10a.

Jillian R Hufgard, Michael T Williams, Matthew R Skelton, Olivera Grubisha, Filipa M Ferreira, Helen Sanger, Mary E Wright, Tracy M Reed-Kessler, Kurt Rasmussen, Ronald S Duman and 1 more

Abstract read
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In one paragraph

Article in Psychopharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

16 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Early-Onset Movement Disorder Syndrome Caused by Biallelic Variants in PDE1B Encoding Phosphodiesterase 1B.Movement disorders : official journal of the Movement Disorder Society · 2025
    Article
  3. Article
  4. CaCell reports · 2024
    Article
  5. Circuit-Wide Gene Network Analysis Reveals Sex-Specific Roles for Phosphodiesterase 1b in Cocaine Addiction.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  6. Article
  7. Article
  8. The Emerging Role of Phosphodiesterases in Movement Disorders.Movement disorders : official journal of the Movement Disorder Society · 2021
    Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Additive antidepressant-like effects of fasting with β-estradiol in mice.Journal of cellular and molecular medicine · 2019
    Article
  14. Article
  15. Review
  16. 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

11 authors at 6 institutions in 2 countries.

Jillian R HufgardDivision of Neurology (MLC 7044), Department of Pediatrics, Cincinnati Children's Research Foundation and University of Cincinnati College of Medicine, 3333 Burnet Ave., Cincinnati, OH, USA.
Michael T WilliamsDivision of Neurology (MLC 7044), Department of Pediatrics, Cincinnati Children's Research Foundation and University of Cincinnati College of Medicine, 3333 Burnet Ave., Cincinnati, OH, USA.
Matthew R SkeltonDivision of Neurology (MLC 7044), Department of Pediatrics, Cincinnati Children's Research Foundation and University of Cincinnati College of Medicine, 3333 Burnet Ave., Cincinnati, OH, USA.
Olivera GrubishaNeuroscience Research Division, Lilly Research Centre, Eli Lilly & Co. Ltd., Windlesham, Surrey, UK.
Filipa M FerreiraNeuroscience Research Division, Lilly Research Centre, Eli Lilly & Co. Ltd., Windlesham, Surrey, UK.
Helen SangerNeuroscience Research Division, Lilly Research Centre, Eli Lilly & Co. Ltd., Windlesham, Surrey, UK.
Mary E WrightDepartment of Biology, Mount Saint Joseph University, Cincinnati, OH, 45233, USA.
Tracy M Reed-KesslerDepartment of Biology, Mount Saint Joseph University, Cincinnati, OH, 45233, USA.
Kurt RasmussenLilly Corporate Center, Lilly Research Laboratories, Indianapolis, IN, 46285, USA.
Ronald S DumanDepartment of Psychiatry, Yale University School of Medicine, 34 Park St., New Haven, CT, 06519-1109, USA.
Charles V VorheesDivision of Neurology (MLC 7044), Department of Pediatrics, Cincinnati Children's Research Foundation and University of Cincinnati College of Medicine, 3333 Burnet Ave., Cincinnati, OH, USA. charles.vorhees@cchmc.org.
Eli Lilly (United Kingdom) · GBUniversity of Cincinnati Medical Center · USMount St. Joseph University · USCincinnati Children's Hospital Medical Center · USEli Lilly (United States) · USYale University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationaleMajor depressive disorder is a leading cause of suicide and disability. Despite this, current antidepressants provide insufficient efficacy in more than 60% of patients. Most current antidepressants are presynaptic reuptake inhibitors; postsynaptic signal regulation has not received as much attention as potential treatment targets.

objectivesWe examined the effects of disruption of the postsynaptic cyclic nucleotide hydrolyzing enzyme, phosphodiesterase (PDE) 1b, on depressive-like behavior and the effects on PDE1B protein in wild-type (WT) mice following stress.

methodsLittermate knockout (KO) and WT mice were tested in locomotor activity, tail suspension (TST), and forced swim tests (FST). FST was also used to compare the effects of two antidepressants, fluoxetine and bupropion, in KO versus WT mice. Messenger RNA (mRNA) expression changes were also determined. WT mice underwent acute or chronic stress and markers of stress and PDE1B expression were examined.

resultsPde1b KO mice exhibited decreased TST and FST immobility. When treated with antidepressants, both WT and KO mice showed decreased FST immobility and the effect was additive in KO mice. Mice lacking Pde1b had increased striatal Pde10a mRNA expression. In WT mice, acute and chronic stress upregulated PDE1B expression while PDE10A expression was downregulated after chronic but not acute stress.

conclusionsPDE1B is a potential therapeutic target for depression treatment because of the antidepressant-like phenotype seen in Pde1b KO mice.

Indexed as

AnimalsAntidepressive AgentsCorpus StriatumCyclic Nucleotide Phosphodiesterases, Type 1DepressionFemaleHindlimb SuspensionImmobilizationMaleMiceMice, Inbred C57BLMice, KnockoutPhosphoric Diester HydrolasesSwimmingUp-RegulationAntidepressive AgentsCyclic Nucleotide Phosphodiesterases, Type 1Pde10a protein, mousePde1b protein, mousePhosphoric Diester HydrolasesForced swim testPDE1BPde1b knockout micePde brain gene expressionPhosphodiesteraseStress resistance

Identifiers

PMID28337525
OpenAlexW2601277655

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.