Evidence map›Paper›PMID 28822057›Full record

ArticleMolecular neurobiology2018

Short-Term Exposure to Enriched Environment in Adult Rats Restores MK-801-Induced Cognitive Deficits and GABAergic Interneuron Immunoreactivity Loss.

Ane Murueta-Goyena, Naiara Ortuzar, Pascual Ángel Gargiulo, José Vicente Lafuente, Harkaitz Bengoetxea

Erratum issuedOpen access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Molecular neurobiology, 2018. 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 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.1field-weighted citation impact, top 27% 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

16 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  5. Enriched environment as a nonpharmacological neuroprotective strategy.Experimental biology and medicine (Maywood, N.J.) · 2023
    Review
  6. Article
  7. Transcranial Ultrasound Stimulation Reverses Behavior Changes and the Expression of Calcium-Binding Protein in a Rodent Model of Schizophrenia.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2022
    Article
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  9. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 3 countries.

Ane Murueta-GoyenaLaNCE, Department of Neuroscience, University of the Basque Country (UPV/EHU), Barrio Sarriena, E-48940, Leioa, Bizkaia, Spain. ane.muruetagoyena@ehu.eus.
Naiara OrtuzarLaNCE, Department of Neuroscience, University of the Basque Country (UPV/EHU), Barrio Sarriena, E-48940, Leioa, Bizkaia, Spain.
Pascual Ángel GargiuloLaboratory of Neurosciences and Experimental Psychology, Area of Pharmacology, Department of Pathology, Faculty of Medical Sciences, National University of Cuyo, National Council of Scientific and Technical Research, Mendoza, Argentina.
José Vicente LafuenteLaNCE, Department of Neuroscience, University of the Basque Country (UPV/EHU), Barrio Sarriena, E-48940, Leioa, Bizkaia, Spain.
Harkaitz BengoetxeaLaNCE, Department of Neuroscience, University of the Basque Country (UPV/EHU), Barrio Sarriena, E-48940, Leioa, Bizkaia, Spain.
University of the Basque Country · ESBioCruces Health research Institute · ESUniversidad Nacional de Cuyo · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Perinatal injections of N-methyl-D-aspartate (NMDA) receptor antagonist in rodents emulate some cognitive impairments and neurochemical alterations, such as decreased GABAergic (gamma aminobutyric acid) interneuron immunoreactivity, also found in schizophrenia. These features are pervasive, and developing neuroprotective or neurorestorative strategies is of special interest. In this work, we aimed to investigate if a short exposure to enriched environment (EE) in early adulthood (P55-P73) was an effective strategy to improve cognitive dysfunction and to restore interneuron expression in medial prefrontal cortex (mPFC) and hippocampus (HPC). For that purpose, we administered MK-801 intraperitoneally to Long Evans rats from postnatal days 10 to 20. Twenty-four hours after the last injection, MK-801 produced a transient decrease in spontaneous motor activity and exploration, but those abnormalities were absent at P24 and P55. The open field test on P73 manifested that EE reduced anxiety-like behavior. In addition, MK-801-treated rats showed cognitive impairment in novel object recognition test that was reversed by EE. We quantified different interneuron populations based on their calcium-binding protein expression (parvalbumin, calretinin, and calbindin), glutamic acid decarboxylase 67, and neuronal nuclei-positive cells by means of unbiased stereology and found that EE enhanced interneuron immunoreactivity up to normal values in MK-801-treated rats. Our results demonstrate that a timely intervention with EE is a powerful tool to reverse long-lasting changes in cognition and neurochemical markers of interneurons in an animal model of schizophrenia.

Indexed as

EnvironmentAge FactorsAnimalsAnimals, NewbornCognitive DysfunctionDizocilpine MaleateExcitatory Amino Acid AntagonistsFemaleGABAergic NeuronsInterneuronsMaleRatsRats, Long-EvansTime FactorsDizocilpine MaleateExcitatory Amino Acid AntagonistsCalcium-binding proteinsCognitive dysfunctionEnriched environmentInterneuronsMK-801

Identifiers

PMID28822057
OpenAlexW2750092076

What OpenQuestion holds

Textmetadata
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.