Evidence map›Paper›PMID 23197707›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2012

Anxiety-like behavior of prenatally stressed rats is associated with a selective reduction of glutamate release in the ventral hippocampus.

Jordan Marrocco, Jérôme Mairesse, Richard Teke Ngomba, Viviana Silletti, Gilles Van Camp, Hammou Bouwalerh, Maria Summa, Anna Pittaluga, Ferdinando Nicoletti, Stefania Maccari and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

36 citing papers in PubMed, 99 citations in OpenAlex.

  1. Article
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  11. Genomic modules and intramodular network concordance in susceptible and resilient male mice across models of stress.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
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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

11 authors at 6 institutions in 2 countries.

Jordan MarroccoNeural Plasticity Team-UMR CNRS/USTL 8576 Structural and Functional Glycobiology Unit, North University of Lille, 59655 Villeneuve d'Ascq France, IRCCS Neuromed, 86077 Pozzilli, Italy.
Jérôme Mairesse
Richard Teke Ngomba
Viviana Silletti
Gilles Van Camp
Hammou Bouwalerh
Maria Summa
Anna Pittaluga
Ferdinando Nicoletti
Stefania Maccari
Sara Morley-Fletcher
Université de Lille · FRCentre National de la Recherche Scientifique · FRUniversity of Genoa · ITIstituto Neurologico Mediterraneo · ITSapienza University of Rome · ITUnité de Glycobiologie Structurale et Fonctionnelle · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Abnormalities of synaptic transmission and plasticity in the hippocampus represent an integral part of the altered programming triggered by early life stress. Prenatally restraint stressed (PRS) rats develop long-lasting biochemical and behavioral changes, which are the expression of an anxious/depressive-like phenotype. We report here that PRS rats showed a selective impairment of depolarization- or kainate-stimulated glutamate and [(3)H]d-aspartate release in the ventral hippocampus, a region encoding memories related to stress and emotions. GABA release was unaffected in PRS rats. As a consequence of reduced glutamate release, PRS rats were also highly resistant to kainate-induced seizures. Abnormalities of glutamate release were associated with large reductions in the levels of synaptic vesicle-related proteins, such as VAMP (synaptobrevin), syntaxin-1, synaptophysin, synapsin Ia/b and IIa, munc-18, and Rab3A in the ventral hippocampus of PRS rats. Anxiety-like behavior in male PRS (and control) rats was inversely related to the extent of depolarization-evoked glutamate release in the ventral hippocampus. A causal relationship between anxiety-like behavior and reduction in glutamate release was demonstrated using a mixture of the mGlu2/3 receptor antagonist, LY341495, and the GABA(B) receptor antagonist, CGP52432, which was shown to amplify depolarization-evoked [(3)H]d-aspartate release in the ventral hippocampus. Bilateral microinfusion of CGP52432 plus LY341495 in the ventral hippocampus abolished anxiety-like behavior in PRS rats. These findings indicate that an impairment of glutamate release in the ventral hippocampus is a key component of the neuroplastic program induced by PRS, and that strategies aimed at enhancing glutamate release in the ventral hippocampus correct the "anxious phenotype" caused by early life stress.

Indexed as

Amino AcidsAnimalsAnxietyBehavior, AnimalBenzylaminesExcitatory Amino Acid AntagonistsFemaleGABA-A Receptor AntagonistsGlutamic AcidHippocampusKainic AcidMaleMunc18 ProteinsPhosphinic AcidsPregnancyPrenatal Exposure Delayed EffectsAmino AcidsBenzylaminesCGP 52432Excitatory Amino Acid AntagonistsGABA-A Receptor AntagonistsGlutamic AcidKainic AcidLY 341495Munc18 ProteinsPhosphinic Acidsrab3A GTP-Binding ProteinR-SNARE ProteinsSynapsinsSynaptophysinSyntaxin 1Xanthenes

Identifiers

PMID23197707
PMCPMC6621858
OpenAlexW2001131875

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.