Evidence map›Paper›PMID 24952323›Full record

ArticleJournal of neuroscience methods2014

Automated touch screen device for recording complex rodent behaviors.

O S Mabrouk, I J Dripps, S Ramani, C Chang, J L Han, K C Rice, E M Jutkiewicz

Abstract read
In one paragraph

Article in Journal of neuroscience methods, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.3field-weighted citation impact, top 50% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  6. Analgesic Efficacy and Hematologic Effects of Robenacoxib in Mice.Journal of the American Association for Laboratory Animal Science : JAALAS · 2018
    Article
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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

7 authors at 3 institutions in 1 country.

O S MabroukNeurolytical LLC, Ann Arbor, MI, United States; Department of Pharmacology, Ann Arbor, MI, United States; Department of Chemistry, University of Michigan, Ann Arbor, MI, United States.
I J DrippsDepartment of Pharmacology, Ann Arbor, MI, United States.
S RamaniDepartment of Pharmacology, Ann Arbor, MI, United States.
C ChangDepartment of Pharmacology, Ann Arbor, MI, United States.
J L HanDepartment of Chemistry, University of Michigan, Ann Arbor, MI, United States.
K C RiceChemical Biology Research Branch, National Institute on Drug Abuse and National Institute on Alcohol Abuse and Alcoholism, Bethesda, MD, United States.
E M JutkiewiczDepartment of Pharmacology, Ann Arbor, MI, United States. Electronic address: ejutkiew@umich.edu.
Michigan Medicine · USUniversity of Michigan–Ann Arbor · USNational Institute on Alcohol Abuse and Alcoholism · US

Funding

Medicinal Chemistry of Drugs Acting on Central and Peripheral Opioid ReceptorsZIADA000527 · NIDA · NATIONAL INSTITUTE ON DRUG ABUSE · PI RICE, KENNER · 2009 to 2025
$23.2M
Intramural NIH HHS ZIA DA000527
6 · The paper itself

Abstract

backgroundMonitoring mouse behavior is a critical step in the development of modern pharmacotherapies. NEW

methodHere we describe the application of a novel method that utilizes a touch display computer (tablet) and software to detect, record, and report fine motor behaviors. A consumer-grade tablet device is placed in the bottom of a specially made acrylic cage allowing the animal to walk on the device (MouseTrapp). We describe its application in open field (for general locomotor studies) which measures step lengths and velocity. The device can perform light-dark (anxiety) tests by illuminating half of the screen and keeping the other half darkened. A divider is built into the lid of the device allowing the animal free access to either side.

resultsTreating mice with amphetamine and the delta opioid peptide receptor agonist SNC80 stimulated locomotor activity on the device. Amphetamine increased step velocity but not step length during its peak effect (40-70min after treatment), thus indicating detection of subtle amphetamine-induced effects. Animals showed a preference (74% of time spent) for the darkened half compared to the illuminated side. COMPARISON WITH EXISTING

methodAnimals were videotaped within the chamber to compare quadrant crosses to detect motion on the device. The slope, duration and magnitude of quadrant crosses tightly correlated with overall locomotor activity as detected by MouseTrapp.

conclusionsWe suggest that modern touch display devices such as MouseTrapp will be an important step toward automation of behavioral analyses for characterizing phenotypes and drug effects.

Indexed as

ActigraphyMicrocomputersMotor ActivitySoftwareAmphetamineAnalgesics, OpioidAnimalsAnxietyBehavior, AnimalBenzamidesBiomechanical PhenomenaCentral Nervous System StimulantsFemaleMaleMice, Inbred C57BLPattern Recognition, Automated4-(alpha-(4-allyl-2,5-dimethyl-1-piperazinyl)-3-methoxybenzyl)-N,N-diethylbenzamideAmphetamineAnalgesics, OpioidBenzamidesCentral Nervous System StimulantsPiperazinesReceptors, Opioid, deltaAnxietyBehaviorLight–dark boxMotor functionMouseMovementOpen fieldTechnology

Identifiers

PMID24952323
PMCPMC4948120
OpenAlexW1974969952

What OpenQuestion holds

Textmetadata
LicenceTDM
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.