Evidence map›Paper›PMID 24651125›Full record

ArticlePloS one2014

Lifetime stress cumulatively programs brain transcriptome and impedes stroke recovery: benefit of sensory stimulation.

Fabíola C R Zucchi, Youli Yao, Yaroslav Ilnytskyy, Jerrah C Robbins, Nasrin Soltanpour, Igor Kovalchuk, Olga Kovalchuk, Gerlinde A S Metz

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-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

10 citing papers in PubMed, 21 citations in OpenAlex.

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4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

8 authors at 2 institutions in 2 countries.

Fabíola C R ZucchiCanadian Centre for Behavioural Neuroscience, University of Lethbridge, Lethbridge, Alberta, Canada; Departments of Medicine and Biological Sciences, University of Mato Grosso State, Cáceres, MT, Brazil.
Youli YaoCanadian Centre for Behavioural Neuroscience, University of Lethbridge, Lethbridge, Alberta, Canada; Department of Biological Sciences, University of Lethbridge, Lethbridge, Alberta, Canada.
Yaroslav IlnytskyyDepartment of Biological Sciences, University of Lethbridge, Lethbridge, Alberta, Canada.
Jerrah C RobbinsCanadian Centre for Behavioural Neuroscience, University of Lethbridge, Lethbridge, Alberta, Canada.
Nasrin SoltanpourCanadian Centre for Behavioural Neuroscience, University of Lethbridge, Lethbridge, Alberta, Canada.
Igor KovalchukDepartment of Biological Sciences, University of Lethbridge, Lethbridge, Alberta, Canada.
Olga KovalchukDepartment of Biological Sciences, University of Lethbridge, Lethbridge, Alberta, Canada.
Gerlinde A S MetzCanadian Centre for Behavioural Neuroscience, University of Lethbridge, Lethbridge, Alberta, Canada.
University of Lethbridge · CAUniversidade do Estado de Mato Grosso · BR

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

Prenatal stress (PS) represents a critical variable affecting lifetime health trajectories, metabolic and vascular functions. Beneficial experiences may attenuate the effects of PS and its programming of health outcomes in later life. Here we investigated in a rat model (1) if PS modulates recovery following cortical ischemia in adulthood; (2) if a second hit by adult stress (AS) exaggerates stress responses and ischemic damage; and (3) if tactile stimulation (TS) attenuates the cumulative effects of PS and AS. Prenatally stressed and non-stressed adult male rats underwent focal ischemic motor cortex lesion and were tested in skilled reaching and skilled walking tasks. Two groups of rats experienced recurrent restraint stress in adulthood and one of these groups also underwent daily TS therapy. Animals that experienced both PS and AS displayed the most severe motor disabilities after lesion. By contrast, TS promoted recovery from ischemic lesion and reduced hypothalamic-pituitary-adrenal axis activity. The data also showed that cumulative effects of adverse and beneficial lifespan experiences interact with disease outcomes and brain plasticity through the modulation of gene expression. Microarray analysis of the lesion motor cortex revealed that cumulative PS and AS interact with genes related to growth factors and transcription factors, which were not affected by PS or lesion alone. TS in PS+AS animals reverted these changes, suggesting a critical role for these factors in activity-dependent motor cortical reorganization after ischemic lesion. These findings suggest that beneficial experience later in life can moderate adverse consequences of early programming to improve cerebrovascular health.

Indexed as

SensationAgingAnimalsBrainBrain IschemiaGene Expression ProfilingGene Expression RegulationHypothalamo-Hypophyseal SystemMaleMotor ActivityMotor CortexMovementOligonucleotide Array Sequence AnalysisPhysical StimulationPituitary-Adrenal SystemRats, Long-Evans

Identifiers

PMID24651125
PMCPMC3961295
OpenAlexW2058052694

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.