Evidence map›Paper›PMID 27285859›Full record

ArticleEndocrinology2016

Neonatal Masculinization Blocks Increased Excitatory Synaptic Input in Female Rat Nucleus Accumbens Core.

Jinyan Cao, David M Dorris, John Meitzen

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
6.4field-weighted citation impact, top 4% 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

32 citing papers in PubMed, 49 citations in OpenAlex.

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  12. Perinatal activation of ERJournal of neurophysiology · 2021
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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

3 authors at 1 institution in 1 country.

Jinyan CaoDepartment of Biological Sciences (J.C., D.M.D., J.M.), North Carolina State University, Raleigh, North Carolina 27695; W.M. Keck Center for Behavioral Biology (J.C., J.M.), North Carolina State University, Raleigh, North Carolina 27695; Center for Human Health and the Environment (J.M.), North Carolina State University, Raleigh, North Carolina 27695; and Comparative Medicine Institute (J.M.), North Carolina State University, Raleigh, North Carolina 27695.
David M DorrisDepartment of Biological Sciences (J.C., D.M.D., J.M.), North Carolina State University, Raleigh, North Carolina 27695; W.M. Keck Center for Behavioral Biology (J.C., J.M.), North Carolina State University, Raleigh, North Carolina 27695; Center for Human Health and the Environment (J.M.), North Carolina State University, Raleigh, North Carolina 27695; and Comparative Medicine Institute (J.M.), North Carolina State University, Raleigh, North Carolina 27695.
John MeitzenDepartment of Biological Sciences (J.C., D.M.D., J.M.), North Carolina State University, Raleigh, North Carolina 27695; W.M. Keck Center for Behavioral Biology (J.C., J.M.), North Carolina State University, Raleigh, North Carolina 27695; Center for Human Health and the Environment (J.M.), North Carolina State University, Raleigh, North Carolina 27695; and Comparative Medicine Institute (J.M.), North Carolina State University, Raleigh, North Carolina 27695.
North Carolina State University · US

Funding

Translational Research Support CoreP30ES025128 · NIEHS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI Andrew R. Binder · 2015 to 2026
$18.3M
Elucidating the mechanisms by which estradiol regulates female striatal neuron excitabilityR01MH109471 · NIMH · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI MEITZEN, JOHN · 2016 to 2020
$1.8M
NIEHS NIH HHS P30 ES025128NIMH NIH HHS R01 MH109471
6 · The paper itself

Abstract

Steroid sex hormones and genetic sex regulate the phenotypes of motivated behaviors and relevant disorders. Most studies seeking to elucidate the underlying neuroendocrine mechanisms have focused on how 17β-estradiol modulates the role of dopamine in striatal brain regions, which express membrane-associated estrogen receptors. Dopamine action is an important component of striatal function, but excitatory synaptic neurotransmission has also emerged as a key striatal substrate and target of estradiol action. Here, we focus on excitatory synaptic input onto medium spiny neurons (MSNs) in the striatal region nucleus accumbens core (AcbC). In adult AcbC, miniature excitatory postsynaptic current (mEPSC) frequency is increased in female compared with male MSNs. We tested whether increased mEPSC frequency in female MSNs exists before puberty, whether this increased excitability is due to the absence of estradiol or testosterone during the early developmental critical period, and whether it is accompanied by stable neuron intrinsic membrane properties. We found that mEPSC frequency is increased in female compared with male MSNs before puberty. Increased mEPSC frequency in female MSNs is abolished after neonatal estradiol or testosterone exposure. MSN intrinsic membrane properties did not differ by sex. These data indicate that neonatal masculinization via estradiol and/or testosterone action is sufficient for down-regulating excitatory synaptic input onto MSNs. We conclude that excitatory synaptic input onto AcbC MSNs is organized long before adulthood via steroid sex hormone action, providing new insight into a mechanism by which sex differences in motivated behavior and other AbcC functions may be generated or compromised.

Indexed as

AnimalsAnimals, NewbornEstradiolExcitatory Postsynaptic PotentialsFemaleFeminizationMaleNucleus AccumbensRatsRats, Sprague-DawleySex CharacteristicsSexual MaturationSynaptic TransmissionEstradiol

Identifiers

PMID27285859
PMCPMC4967116
OpenAlexW2414923741

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.