Evidence map›Paper›PMID 21092742›Full record

ArticlePhysiology & behavior2011

Disruption of the neuregulin 1 gene in the rat alters HPA axis activity and behavioral responses to environmental stimuli.

S B Taylor, A R Taylor, J A Markham, A M Geurts, B Z Kanaskie, J I Koenig

Abstract read
In one paragraph

Article in Physiology & behavior, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 32% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

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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

6 authors at 2 institutions in 1 country.

S B TaylorProgram in Neuroscience, University of Maryland School of Medicine, Baltimore, MD 21201, USA. staylor@mprc.umaryland.edu
A R Taylor
J A Markham
A M Geurts
B Z Kanaskie
J I Koenig
University of Maryland, Baltimore · USMedical College of Wisconsin · US

Funding

PHYSIOGENOMICS OF STRESSORS IN DERIVED CONSOMIC RATSU01HL066579 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI JACOB, HOWARD J · 2000 to 2007
$26.6M
Tretment of negative symptoms and cognitive impairment in schizopreniaP50MH082999 · NIMH · UNIVERSITY OF MARYLAND BALTIMORE · PI CARPENTER, WILLIAM T. · 2008 to 2012
$9.7M
Multidisciplinary Schizophrenia Research TrainingT32MH067533 · NIMH · UNIVERSITY OF MARYLAND BALTIMORE · PI CARPENTER, WILLIAM T., ELMER, GREGORY I · 2004 to 2025
$4.3M
Neuropeptide Involvement In Male Social BehaviorR01MH073826 · NIMH · UNIVERSITY OF MARYLAND BALTIMORE · PI KOENIG, JAMES I · 2006 to 2009
$978k
Neurobiology of Stress Workshop 2010R13MH090623 · NIMH · UNIVERSITY OF COLORADO · PI HERMAN, JAMES P, KOENIG, JAMES I · 2010 to 2010
$19k
NHLBI NIH HHS 5U01HL066579NHLBI NIH HHS U01 HL066579NIDA NIH HHS N01 DA059909NIMH NIH HHS MH73826NIMH NIH HHS MH82999NIMH NIH HHS P50 MH082999NIMH NIH HHS R01 MH073826NIMH NIH HHS R13 MH090623NIMH NIH HHS R13MH090623NIMH NIH HHS T32 MH067533
6 · The paper itself

Abstract

Exposure to stress can result in an increased risk for psychiatric disorders, especially among genetically predisposed individuals. Neuregulin 1 (NRG1) is a susceptibility gene for schizophrenia and is also associated with psychotic bipolar disorder. In the rat, the neurons of the hypothalamic paraventricular nucleus show strong expression of Nrg1 mRNA. In patients with schizophrenia, a single nucleotide polymorphism in the 5' region of NRG1 interacts with psychosocial stress to affect reactivity to expressed emotion. However, there is virtually no information on the role of NRG1 in hypothalamic-pituitary-adrenal axis function, and whether the protein is expressed in the paraventricular nucleus is unknown. The present studies utilize a unique line of Nrg1 hypomorphic rats (Nrg1(Tn)) generated by gene trapping with the Sleeping Beauty transposon. We first established that the Nrg1(Tn) rats displayed reduced expression of both the mRNA and protein corresponding to the Type II NRG1 isoform. After confirming, using wild type animals, that Type II NRG1 is expressed in the neurocircuitry involved in regulating hypothalamic-pituitary-adrenal axis responses to environmental stimuli, the Nrg1(Tn) rats were then used to test the hypothesis that altered expression of Type II NRG1 disrupts stress regulation and reactivity. In support of this hypothesis, Nrg1(Tn) rats have disrupted basal and acute stress recovery corticosterone secretion, differential changes in expression of glucocorticoid receptors in the pituitary, paraventricular nucleus and hippocampus, and a failure to habituate to an open field. Together, these findings point to NRG1 as a potential novel regulator of neuroendocrine responses to stress as well as behavioral reactivity.

Indexed as

EnvironmentAnalysis of VarianceAnimalsAnimals, NewbornBehavior, AnimalCorticosteroneExploratory BehaviorFemaleGlucocorticoidsHabituation, PsychophysiologicHypothalamo-Hypophyseal SystemMaleMaternal BehaviorMutationNeuregulin-1Pituitary-Adrenal SystemCorticosteroneGlucocorticoidsNeuregulin-1Receptors, MineralocorticoidRNA, Messenger

Identifiers

PMID21092742
PMCPMC3081908
OpenAlexW2052356288

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.