Evidence map›Paper›PMID 29867437›Full record

ArticleFrontiers in synaptic neuroscience2018

Cell-Type Specific Development of the Hyperpolarization-Activated Current, Ih, in Prefrontal Cortical Neurons.

Sha-Sha Yang, Yan-Chun Li, Austin A Coley, Linda A Chamberlin, Ping Yu, Wen-Jun Gao

Open access · goldAbstract read
In one paragraph

Article in Frontiers in synaptic neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.9field-weighted citation impact, top 32% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  11. Distinct Roles for Prefrontal Dopamine D1 and D2 Neurons in Social Hierarchy.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  12. Review
  13. Review
  14. Constitutive Genetic Deletion ofBrain sciences · 2020
    Article
  15. Disruption of Critical Period Plasticity in a Mouse Model of Neurofibromatosis Type 1.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  16. 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 2 institutions in 2 countries.

Sha-Sha YangBeijing Key Laboratory of Learning and Cognition, College of Psychology, Capital Normal University, Beijing, China.
Yan-Chun LiDepartment of Neurobiology and Anatomy, College of Medicine, Drexel University, Philadelphia, PA, United States.
Austin A ColeyDepartment of Neurobiology and Anatomy, College of Medicine, Drexel University, Philadelphia, PA, United States.
Linda A ChamberlinDepartment of Neurobiology and Anatomy, College of Medicine, Drexel University, Philadelphia, PA, United States.
Ping YuBeijing Key Laboratory of Learning and Cognition, College of Psychology, Capital Normal University, Beijing, China.
Wen-Jun GaoDepartment of Neurobiology and Anatomy, College of Medicine, Drexel University, Philadelphia, PA, United States.
Drexel University · USCapital Normal University · CN

Funding

Development of NMDAR hypofunction and cognitive deficitsR01MH085666 · NIMH · DREXEL UNIVERSITY · PI GAO, WEN-JUN · 2009 to 2018
$3.8M
Targeting parvalbumin neurons in the PFC for cognitive deficitsR21MH111609 · NIMH · DREXEL UNIVERSITY · PI GAO, WEN-JUN · 2017 to 2018
$430k
Role of prefrontal cortical dopamine in aggressionR21MH110678 · NIMH · DREXEL UNIVERSITY · PI GAO, WEN-JUN · 2016 to 2017
$425k
NIMH NIH HHS R01 MH085666NIMH NIH HHS R21 MH110678NIMH NIH HHS R21 MH111609
6 · The paper itself

Abstract

H-current, also known as hyperpolarization-activated current (Ih), is an inward current generated by the hyperpolarization-activated cyclic nucleotide-gated (HCN) cation channels. Ih plays an essential role in regulating neuronal properties, synaptic integration and plasticity, and synchronous activity in the brain. As these biological factors change across development, the brain undergoes varying levels of vulnerability to disorders like schizophrenia that disrupt prefrontal cortex (PFC)-dependent function. However, developmental changes in Ih in PFC neurons remains untested. Here, we examine Ih in pyramidal neurons vs. gamma-aminobutyric acid (GABA)ergic parvalbumin-expressing (PV+) interneurons in developing mouse PFC. Our findings show that the amplitudes of Ih in these cell types are identical during the juvenile period but differ at later time points. In pyramidal neurons, Ih amplitude significantly increases from juvenile to adolescence and follows a similar trend into adulthood. In contrast, the amplitude of Ih in PV+ interneurons decreases from juvenile to adolescence, and does not change from adolescence to adulthood. Moreover, the kinetics of HCN channels in pyramidal neurons is significantly slower than in PV+ interneurons, with a gradual decrease in pyramidal neurons and a gradual increase in PV+ cells across development. Our study reveals distinct developmental trajectories of Ih in pyramidal neurons and PV+ interneurons. The cell-type specific alteration of Ih during the critical period from juvenile to adolescence reflects the contribution of Ih to the maturation of the PFC and PFC-dependent function. These findings are essential for a better understanding of normal PFC function, and for elucidating Ih's crucial role in the pathophysiology of neurodevelopmental disorders.

Indexed as

developmentGABAergic interneuronsHCN channelH-currentmouseparvalbuminprefrontal cortexpyramidal neurons

Identifiers

PMID29867437
PMCPMC5958189
OpenAlexW2800215535

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.