Evidence map›Paper›PMID 32950210›Full record

ArticleBiological psychiatry2021

Vulnerable and Resilient Phenotypes in a Mouse Model of Anorexia Nervosa.

Jeff A Beeler, Devry Mourra, Roseanna M Zanca, Abigail Kalmbach, Celia Gellman, Benjamin Y Klein, Rebecca Ravenelle, Peter Serrano, Holly Moore, Stephen Rayport and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Biological psychiatry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.8field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 56 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 6 institutions in 2 countries.

Jeff A BeelerDepartment of Psychology, Queens College, City University of New York, Flushing, New York; Psychology Program, The Graduate Center, City University of New York, New York, New York; Biology Program, The Graduate Center, City University of New York, New York. Electronic address: jbeeler@qc.cuny.edu.
Devry MourraDepartment of Psychology, Queens College, City University of New York, Flushing, New York; Psychology Program, The Graduate Center, City University of New York, New York, New York.
Roseanna M ZancaPsychology Program, The Graduate Center, City University of New York, New York, New York; Department of Psychology, Hunter College, City University of New York, New York.
Abigail KalmbachDepartment of Psychiatry, Columbia University, New York, New York.
Celia GellmanDepartment of Psychiatry, Columbia University, New York, New York; Department of Molecular Therapeutics, New York State Psychiatric Institute, New York, New York.
Benjamin Y KleinDepartment of Psychiatry, Columbia University, New York, New York; Developmental Neuroscience, New York State Psychiatric Institute, New York, New York; Department of Microbiology and Molecular Genetics, Hebrew University, Jerusalem, Israel.
Rebecca RavenelleBiology Program, The Graduate Center, City University of New York, New York.
Peter SerranoPsychology Program, The Graduate Center, City University of New York, New York, New York; Department of Psychology, Hunter College, City University of New York, New York.
Holly MooreDepartment of Psychiatry, Columbia University, New York, New York; Integrative Neuroscience, New York State Psychiatric Institute, New York, New York; National Institute on Drug Abuse, National Institutes of Health, Bethesda, Maryland.
Stephen RayportDepartment of Psychiatry, Columbia University, New York, New York; Department of Molecular Therapeutics, New York State Psychiatric Institute, New York, New York.
Susana MingoteDepartment of Psychiatry, Columbia University, New York, New York; Department of Molecular Therapeutics, New York State Psychiatric Institute, New York, New York; Advanced Science Research Center, The Graduate Center, City University of New York, New York.
Nesha S BurghardtPsychology Program, The Graduate Center, City University of New York, New York, New York; Department of Psychology, Hunter College, City University of New York, New York; Department of Psychiatry, Columbia University, New York, New York. Electronic address: nb844@hunter.cuny.edu.
The Graduate Center, CUNY · USNew York Psychoanalytic Society and Institute · USQueens College, CUNY · USColumbia University · USHebrew University of Jerusalem · ILNational Institutes of Health · US

Funding

RISE Program Hunter College Option IIIR25GM060665 · NIGMS · HUNTER COLLEGE · PI ORTIZ, BENJAMIN D.,, SERRANO, PETER A · 2000 to 2022
$22.8M
Basic and Translational Research Center for Reducing Health DisparitiesG12MD007599 · NIMHD · HUNTER COLLEGE · PI ANGULO, JESUS A · 2012 to 2017
$14.6M
Training in Schizophrenia and Psychotic Disorders: From Animal Models to PatientsT32MH018870 · NIMH · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Guillermo Horga, Christoph Kellendonk · 1988 to 2026
$9.8M
Dopamine Dysfunction in SchizophreniaP50MH086404 · NIMH · NEW YORK STATE PSYCHIATRIC INSTITUTE DBA RESEARCH FOUNDATION FOR MENTAL HYGIENE, INC · PI ABI-DARGHAM, ANISSA · 2010 to 2014
$9.4M
BP-ENDURE at Hunter and NYUR25NS080686 · NINDS · HUNTER COLLEGE · PI Nesha Star Burghardt, GLENN E SCHAFE · 2012 to 2026
$9.2M
Dissecting contributions of different D2R populations to activity and appetiteR15DA046058 · NIDA · QUEENS COLLEGE · PI BEELER, JEFF A. · 2018 to 2018
$462k
Circuit-Level Regulation of Fear and Safety Learning in Chronically Stressed MiceR21MH114182 · NIMH · HUNTER COLLEGE · PI BURGHARDT, NESHA STAR, LIKHTIK, EKATERINA · 2018 to 2019
$429k
NIDA NIH HHS R15 DA046058NIGMS NIH HHS R25 GM060665NIMHD NIH HHS G12 MD007599NIMH NIH HHS P50 MH086404NIMH NIH HHS R21 MH114182NIMH NIH HHS T32 MH018870NINDS NIH HHS R25 NS080686
6 · The paper itself

Abstract

backgroundIncreased physical activity is a common feature of anorexia nervosa (AN). Although high activity levels are associated with greater risk of developing AN, particularly when combined with dieting, most individuals who diet and exercise maintain a healthy body weight. It is unclear why some individuals develop AN while most do not. A rodent model of resilience and vulnerability to AN would be valuable to research. Dopamine, which is believed to play a crucial role in AN, regulates both reward and activity and may modulate vulnerability.

methodsAdolescent and young adult female C57BL/6N mice were tested in the activity-based anorexia (ABA) model, with an extended period of food restriction in adult mice. ABA was also tested in dopamine transporter knockdown mice and wild-type littermates. Mice that adapted to conditions and maintained a stable body weight were characterized as resilient.

resultsIn adults, vulnerable and resilient phenotypes emerged in both the ABA and food-restricted mice without wheels. Vulnerable mice exhibited a pronounced increase in running throughout the light cycle, which dramatically peaked prior to requiring removal from the experiment. Resilient mice exhibited an adaptive decrease in total running, appropriate food anticipatory activity, and increased consumption, thereby achieving stable body weight. Hyperdopaminergia accelerated progression of the vulnerable phenotype.

conclusionsOur demonstration of distinct resilient and vulnerable phenotypes in mouse ABA significantly advances the utility of the model for identifying genes and neural substrates mediating AN risk and resilience. Modulation of dopamine may play a central role in the underlying circuit.

Indexed as

Anorexia NervosaAnimalsAnorexiaDisease Models, AnimalFemaleMiceMice, Inbred C57BLPhenotypeActivity-based anorexiaAnorexia nervosaDopamineExerciseFood restrictionHyperdopaminergicResilienceStarvationVulnerability

Identifiers

PMID32950210
PMCPMC7855473
OpenAlexW3042808987

What Socratic 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 Socratic graph.