Evidence map›Paper›PMID 39532944›Full record

ArticleScientific reports2024

Sex-dependent effects of early life sensory overstimulation on later life behavioral function in rats.

Abishag Porras, Paolaenid Rodney-Hernández, Jeffy Jackson, Christine H Nguyen, Millie Rincón-Cortés

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Hearing and early life adversity: effects of developmental stress on sensory processing.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    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.

Abishag PorrasDepartment of Neuroscience, School of Behavioral and Brain Sciences, University of Texas at Dallas, Richardson, TX, 75080, USA. abi.porras@utdallas.edu.
Paolaenid Rodney-HernándezDepartment of Neuroscience, School of Behavioral and Brain Sciences, University of Texas at Dallas, Richardson, TX, 75080, USA.
Jeffy JacksonDepartment of Neuroscience, School of Behavioral and Brain Sciences, University of Texas at Dallas, Richardson, TX, 75080, USA.
Christine H NguyenDepartment of Neuroscience, School of Behavioral and Brain Sciences, University of Texas at Dallas, Richardson, TX, 75080, USA.
Millie Rincón-CortésDepartment of Neuroscience, School of Behavioral and Brain Sciences, University of Texas at Dallas, Richardson, TX, 75080, USA. millie.rincon-cortes@utdallas.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Children today are immersed in electronic technology shortly after birth as they now begin regularly watching television earlier than they did in the past. Many new programs geared towards infants contain lots of lights, color, and sounds, which may constitute a form of sensory overstimulation (SOS) that leads to cognitive and behavioral changes in children and adolescents. Here, we examined the impact of early life SOS exposure on later life behavioral and cognitive function in rodents by exposing developing male and female rats to excessive audiovisual stimulation from postnatal days (PND) 10-40 and assessing anxiety-like behavior, social motivation, compulsive behavior, and spatial learning/cognition from PND 50-60. To evaluate potential SOS effects on hypothalamic-pituitary-adrenal (HPA)-axis function, levels of the stress hormone corticosterone (CORT) were measured at 3 timepoints (e.g., PND 23, 41, 61) post-SOS exposure. Sensory overstimulated males exhibited reduced anxiety-like and compulsive behavior compared to controls, whereas females exhibited reduced social motivation but enhanced spatial learning/cognition compared to controls. No differences in baseline CORT levels were found at any age tested, suggesting no impact of early life SOS on later life basal HPA-axis function. Our results demonstrate sex-specific effects of early life SOS on distinct behavioral domains in early adult rats.

Indexed as

AnxietyBehavior, AnimalCorticosteroneAnimalsCognitionCompulsive BehaviorFemaleHypothalamo-Hypophyseal SystemMalePhotic StimulationPituitary-Adrenal SystemRatsSex CharacteristicsSex FactorsSpatial LearningCorticosterone

Identifiers

PMID39532944
PMCPMC11557974

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Registered trials

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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.