Evidence map›Paper›PMID 25284318›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2015

Excitatory synaptic function and plasticity is persistently altered in ventral tegmental area dopamine neurons after prenatal ethanol exposure.

Kathryn Hausknecht, Samir Haj-Dahmane, Ying-Ling Shen, Paul Vezina, Cynthia Dlugos, Roh-Yu Shen

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

25 citing papers in PubMed, 37 citations in OpenAlex.

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  17. Neurobiology of maternal regulation of infant fear: the role of mesolimbic dopamine and its disruption by maltreatment.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2019
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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 1 country.

Kathryn HausknechtResearch Institute on Addictions, University at Buffalo, State University of New York, Buffalo, NY, USA.
Samir Haj-DahmaneResearch Institute on Addictions, University at Buffalo, State University of New York, Buffalo, NY, USA.
Ying-Ling ShenResearch Institute on Addictions, University at Buffalo, State University of New York, Buffalo, NY, USA.
Paul VezinaDepartment of Psychiatry and Behavioral Neurosciences, University of Chicago, Chicago, IL, USA.
Cynthia DlugosDepartment of Pathology and Anatomical Sciences, University at Buffalo, Buffalo, NY, USA.
Roh-Yu ShenResearch Institute on Addictions, University at Buffalo, State University of New York, Buffalo, NY, USA.
University at Buffalo, State University of New York · USUniversity of Chicago · US

Funding

Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
Sensitization and Stimulant Self-AdministrationR01DA009397 · NIDA · UNIVERSITY OF CHICAGO · PI VEZINA, PAUL R · 1995 to 2017
$4.0M
Addiction Propensity After Prenatal Ethanol ExposureR01AA019482 · NIAAA · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI SHEN, ROH-YU · 2011 to 2015
$1.7M
DOPAMINE FUNCTION AFTER PRENATAL ETHANOL EXPOSURER01AA012435 · NIAAA · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI SHEN, ROH-YU · 1999 to 2008
$1.6M
NCATS NIH HHS UL1 TR000430NIAAA NIH HHS AA019482NIAAA NIH HHS AA12435NIAAA NIH HHS R01 AA012435NIAAA NIH HHS R01 AA019482NIDA NIH HHS R01 DA009397
6 · The paper itself

Abstract

Prenatal ethanol exposure (PE) is one of the developmental factors leading to increased addiction propensity (risk). However, the neuronal mechanisms underlying this effect remain unknown. We examined whether increased excitatory synaptic transmission in ventral tegmental area (VTA) dopamine (DA) neurons, which is associated with drug addiction, was impacted by PE. Pregnant rats were exposed to ethanol (0 or 6 g/kg/day) via intragastric intubation from gestational day 8-20. Amphetamine self-administration, whole-cell recordings, and electron microscopy were performed in male offspring between 2 and 12-week-old. The results showed enhanced amphetamine self-administration in PE animals. In PE animals, we observed a persistent augmentation in calcium-permeable AMPA receptor (CP-AMPAR) expression, indicated by increased rectification and reduced decay time of AMPAR-mediated excitatory postsynaptic currents (AMPAR-EPSCs), enhanced depression of AMPAR-EPSCs by NASPM (a selective CP-AMPAR antagonist), and increased GluA3 subunits in VTA DA neuron dendrites. Increased CP-AMPAR expression in PE animals led to enhanced excitatory synaptic strength and the induction of CP-AMPAR-dependent long-term potentiation (LTP), an anti-Hebbian form of LTP. These observations suggest that, in PE animals, increased excitatory synaptic strength in VTA DA neurons might be susceptible to further strengthening even in the absence of impulse flow. The PE-induced persistent increase in CP-AMPAR expression, the resulting enhancement in excitatory synaptic strength, and CP-AMPAR-dependent LTP are similar to effects observed after repeated exposure to drugs of abuse, conditions known to increase addiction risk. Therefore, these mechanisms could be important neuronal substrates underlying PE-induced enhancement in amphetamine self-administration and increased addiction risk in individuals with fetal alcohol spectrum disorders.

Indexed as

Adrenergic AgentsAmphetamineAnalysis of VarianceAnimalsBiophysicsCentral Nervous System DepressantsDopaminergic NeuronsElectric StimulationEthanolExcitatory Postsynaptic PotentialsFemaleIn Vitro TechniquesMaleMicroscopy, Electron, TransmissionPatch-Clamp TechniquesPregnancyAdrenergic AgentsAmphetamineCentral Nervous System DepressantsEthanolReceptors, AMPATyrosine 3-Monooxygenase

Identifiers

PMID25284318
PMCPMC4330503
OpenAlexW2033961862

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.