Evidence map›Paper›PMID 22366076›Full record

ArticleNeuropharmacology2012

Neonatal exposure to phenobarbital potentiates schizophrenia-like behavioral outcomes in the rat.

S K Bhardwaj, P A Forcelli, G Palchik, K Gale, L K Srivastava, A Kondratyev

Abstract readComparative Study
In one paragraph

Article in Neuropharmacology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 2 pooled it
1.7field-weighted citation impact, top 17% 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

37 citing papers in PubMed, 2 syntheses or guidelines pooled it, 52 citations in OpenAlex.

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  12. Clonidine versus phenobarbital as adjunctive therapy for neonatal abstinence syndrome.Journal of perinatology : official journal of the California Perinatal Association · 2020
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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 2 institutions in 2 countries.

S K BhardwajDouglas Mental Health University Institute, Department of Psychiatry, McGill University, Montreal, Quebec, Canada.
P A Forcelli
G Palchik
K Gale
L K Srivastava
A Kondratyev
Georgetown University · USDouglas Mental Health University Institute · CA

Funding

Neonatal Seizure Therapy and Susceptibility to SchizophreniaR21MH079991 · NIMH · GEORGETOWN UNIVERSITY · PI KONDRATYEV, ALEXEI D · 2007 to 2008
$373k
Striatal Sequelae of Perinatal Anticonvulsant Drug TreatmentF31NS066822 · NINDS · GEORGETOWN UNIVERSITY · PI FORCELLI, PATRICK ALEXANDER · 2009 to 2011
$58k
CIHR MOP-68922NIMH NIH HHS MH02040NIMH NIH HHS R21 MH079991NINDS NIH HHS F31 NS066822NINDS NIH HHS NS066822
6 · The paper itself

Abstract

Previous work has indicated an association between seizures early in life and increased risk of psychiatric disorders, including schizophrenia. However, because early-life seizures are commonly treated with antiepileptic drugs (AEDs) such as phenobarbital, the possibility that drug treatment may affect later-life psychiatric outcomes needs to be evaluated. We therefore tested the hypothesis that phenobarbital exposure in the neonatal rat increases the risk of schizophrenia-like behavioral abnormalities in adulthood. Thus, in this study, we examined the effects of a single acute neonatal exposure to phenobarbital on adult behavioral outcomes in the rat neonatal ventral hippocampal (nVH) lesion model of schizophrenia. We compared these outcomes to those in rats a) without nVH lesions and b) with nVH lesions, without phenobarbital. The tasks used for behavioral evaluation were: amphetamine-induced locomotion, prepulse inhibition, elevated plus-maze, and novel object recognition task. We found that neonatal phenobarbital treatment (in the absence of nVH lesions) was sufficient to disrupt sensorimotor gating (as tested by prepulse inhibition) in adulthood to an extent equivalent to nVH lesions. Additionally, neonatal phenobarbital exposure enhanced the locomotor response to amphetamine in adult animals with and without nVH lesions. Our findings suggest that neonatal exposure to phenobarbital can predispose to schizophrenia-like behavioral abnormalities. Our findings underscore the importance of examining AED exposure early in life as a potential risk factor for later-life neuropsychiatric abnormalities in clinical populations.

Indexed as

Age FactorsAnimalsAnimals, NewbornFemalePhenobarbitalPregnancyRatsRats, Sprague-DawleySchizophreniaPhenobarbital

Identifiers

PMID22366076
PMCPMC3318973
OpenAlexW2087643578

What OpenQuestion holds

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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.