Evidence map›Paper›PMID 35185478›Full record

ArticleFrontiers in neural circuits2022

Alterations of the Hippocampal Networks in Valproic Acid-Induced Rat Autism Model.

Veronika Bódi, Tímea Májer, Viktor Kelemen, Ildikó Világi, Attila Szűcs, Petra Varró

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neural circuits, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 23 citations in OpenAlex.

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  8. Long-Term Epigenetic Regulation ofInternational journal of molecular sciences · 2024
    Article
  9. Article
  10. The effect of inhibiting hindbrain A2 noradrenergic neurons by 6-Hydroxydopamine on lipopolysaccharide-treated male rats autistic animal model.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2024
    Article
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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 1 institution in 1 country.

Veronika BódiEx vivo Electrophysiology Laboratory, Department of Physiology and Neurobiology, Institute of Biology, Eötvös Loránd University, Budapest, Hungary.
Tímea MájerEx vivo Electrophysiology Laboratory, Department of Physiology and Neurobiology, Institute of Biology, Eötvös Loránd University, Budapest, Hungary.
Viktor KelemenEx vivo Electrophysiology Laboratory, Department of Physiology and Neurobiology, Institute of Biology, Eötvös Loránd University, Budapest, Hungary.
Ildikó VilágiEx vivo Electrophysiology Laboratory, Department of Physiology and Neurobiology, Institute of Biology, Eötvös Loránd University, Budapest, Hungary.
Attila SzűcsEx vivo Electrophysiology Laboratory, Department of Physiology and Neurobiology, Institute of Biology, Eötvös Loránd University, Budapest, Hungary.
Petra VarróEx vivo Electrophysiology Laboratory, Department of Physiology and Neurobiology, Institute of Biology, Eötvös Loránd University, Budapest, Hungary.
Eötvös Loránd University · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autism Spectrum Disorder (ASD) is one of the most frequently diagnosed neurodevelopmental disorders, characterized among others by impairments in social interactions and repetitive behavior. According to one of the leading hypotheses about its origin, ASD is caused by the imbalance of excitatory and inhibitory circuit activity. ASD-related morphological and functional changes can be observed in several brain regions i.e., in the prefrontal cortex and the hippocampus. It is well-established that prenatal valproic-acid (VPA) exposure of rats on day 12.5 leads to neurodevelopmental alterations with autism-like clinical and behavioral symptoms. The aim of this study was to investigate potential changes in the excitability of neuronal networks and individual neurons of the hippocampus elicited by prenatal VPA treatment. As there are marked sex differences in ASD, offspring of both sexes were systematically tested, using two different age groups, to elucidate eventual differences in neurodevelopment after VPA treatment. Excitatory connections and long-term synaptic plasticity as well as intrinsic excitability of CA1 pyramidal cells were examined. Pregnant female Wistar rats received saline or 500 mg/kg VPA i. p. on gestation day 12.5. Brain slices of 6-week-old and 3-month-old offspring were investigated using extra- and intracellular electrophysiological techniques. Field potential- and whole-cell patch clamp recordings were carried out to measure network excitability and single cell activity in the CA1 region hippocampus. Enhanced excitability of hippocampal networks was detected in the 6-week-old VPA-treated male rats; however, this change could not be observed in 3-month-old males. Intrinsic excitability of single neurons, however, was increased in 3-month-old males. In 6-week-old treated females, the most prominent effect of VPA was an increase in voltage sag, to a similar degree to the neurons of the older age group. In 3-month-old females, a network excitability increase could be demonstrated, in a lesser degree than in younger males. It can be concluded, that VPA treatment had diverse effects on hippocampal excitability depending on the sex and the age of the animals. We found that certain alterations manifested in 6-week-old rats were compensated later, on the other hand, other changes persisted until the age of 3 months.

Indexed as

Autism Spectrum DisorderAutistic DisorderPrenatal Exposure Delayed EffectsAnimalsDisease Models, AnimalFemaleHippocampusMalePregnancyRatsRats, WistarValproic AcidValproic Acidautism (ASD)electrophysiologyhippocampuspatch clampVPA

Identifiers

PMID35185478
PMCPMC8854362
OpenAlexW4210312715

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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.