Evidence map›Paper›PMID 25568126›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2015

Overexpression of the type 1 adenylyl cyclase in the forebrain leads to deficits of behavioral inhibition.

Xuanmao Chen, Hong Cao, Amit Saraf, Larry S Zweifel, Daniel R Storm

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.0field-weighted citation impact, top 29% 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

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
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  4. CaFrontiers in pharmacology · 2022
    Review
  5. Article
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  8. Induction of activity synchronization among primed hippocampal neurons out of random dynamics is key for trace memory formation and retrieval.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
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  12. Article
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  14. Article
  15. Type 3 adenylyl cyclase: a key enzyme mediating the cAMP signaling in neuronal cilia.International journal of physiology, pathophysiology and pharmacology · 2016
    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

5 authors at 2 institutions in 2 countries.

Xuanmao ChenDepartment of Pharmacology, School of Medicine, University of Washington, Seattle, Washington 98195, chenx8@uw.edu dstorm@uw.edu.
Hong CaoDepartment of Pharmacology, School of Medicine, University of Washington, Seattle, Washington 98195, Institute of Neurobiology, Institute of Brain Science and State Key Laboratory of Medical Neurobiology, Shanghai Medical College, Fudan University, Shanghai 200032, China.
Amit SarafDepartment of Pharmacology, School of Medicine, University of Washington, Seattle, Washington 98195.
Larry S ZweifelDepartment of Pharmacology, School of Medicine, University of Washington, Seattle, Washington 98195.
Daniel R StormDepartment of Pharmacology, School of Medicine, University of Washington, Seattle, Washington 98195, chenx8@uw.edu dstorm@uw.edu.
University of Washington · USShanghai Medical College of Fudan University · CN

Funding

REGULATION OF CAMP TRANSIENTS IN NEURONSR01DC004156 · NIDCD · UNIVERSITY OF WASHINGTON · PI STORM, DANIEL R · 1999 to 2013
$4.3M
Memory Enhancement by A Genetic Increase in cAMP SignalsR01MH073601 · NIMH · UNIVERSITY OF WASHINGTON · PI STORM, DANIEL R · 2006 to 2015
$3.5M
Functional Mapping of Dopamine-Dependent Fear Circuitry Through Advanced GeneticR01MH094536 · NIMH · UNIVERSITY OF WASHINGTON · PI ZWEIFEL, LARRY S · 2011 to 2015
$2.3M
Cell type-specific calcium imaging during hippocampus-dependent memoryR21MH098177 · NIMH · UNIVERSITY OF WASHINGTON · PI ZWEIFEL, LARRY S · 2012 to 2013
$417k
NIDCD NIH HHS DC004156NIDCD NIH HHS R01 DC004156NIMH NIH HHS MH073601NIMH NIH HHS MH098177NIMH NIH HHS R01 MH073601NIMH NIH HHS R01 MH094536NIMH NIH HHS R21 MH098177
6 · The paper itself

Abstract

The type 1 adenylyl cyclase (AC1) is an activity-dependent, calcium-stimulated adenylyl cyclase expressed in the nervous system that is implicated in memory formation. We examined the locomotor activity, and impulsive and social behaviors of AC1+ mice, a transgenic mouse strain overexpressing AC1 in the forebrain. Here we report that AC1+ mice exhibit hyperactive behaviors and demonstrate increased impulsivity and reduced sociability. In contrast, AC1 and AC8 double knock-out mice are hypoactive, and exhibit increased sociability and reduced impulsivity. Interestingly, the hyperactivity of AC1+ mice can be corrected by valproate, a mood-stabilizing drug. These data indicate that increased expression of AC1 in the forebrain leads to deficits in behavioral inhibition.

Indexed as

Gene Expression Regulation, EnzymologicInhibition, PsychologicalAdenylyl CyclasesAnimalsMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicPrepulse InhibitionProsencephalonRandom Allocationadenylyl cyclase 1Adenylyl CyclasesADHDbehavioral inhibitionhyperactivityimpulsivitysociabilitytype I adenylyl cyclase

Identifiers

PMID25568126
PMCPMC4287152
OpenAlexW2084438520

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.