Evidence map›Paper›PMID 27194328›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2016

Npas1+ Pallidal Neurons Target Striatal Projection Neurons.

Kelly E Glajch, Daniel A Kelver, Daniel J Hegeman, Qiaoling Cui, Harry S Xenias, Elizabeth C Augustine, Vivian M Hernández, Neha Verma, Tina Y Huang, Minmin Luo and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed, 1 pooled it
7.2field-weighted citation impact, top 3% 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

62 citing papers in PubMed, 1 synthesis or guideline pooled it, 120 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Cognitive functions of the GPe.Trends in neurosciences · 2026
    Review
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  11. Reciprocal projections between the globus pallidus externa and cortex span motor and nonmotor regions.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  12. Article
  13. Article
  14. Article
  15. Neuronal PAS domain 1 identifies a major subpopulation of wakefulness-promoting GABAergic neurons in the basal forebrain.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  16. Article
  17. Review
  18. Article
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2 more citing papers are in PubMed but not listed here.

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

12 authors at 2 institutions in 2 countries.

Kelly E GlajchDepartment of Physiology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611.
Daniel A KelverDepartment of Physiology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611.ORCID 0000-0001-9136-5440
Daniel J HegemanDepartment of Physiology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611.
Qiaoling CuiDepartment of Physiology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611.
Harry S XeniasDepartment of Physiology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611.ORCID 0000-0002-9502-0973
Elizabeth C AugustineDepartment of Physiology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611.
Vivian M HernándezDepartment of Physiology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611.
Neha VermaDepartment of Physiology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611.
Tina Y HuangDepartment of Physiology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611.
Minmin LuoNational Institute of Biological Sciences, Beijing 102206, China, School of Life Sciences, Tsinghua University, Beijing 100084, China, and.ORCID 0000-0003-3535-6624
Nicholas J JusticeInstitute of Molecular Medicine, University of Texas, Houston, Texas 77030.
C Savio ChanDepartment of Physiology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611, saviochan@gmail.com.ORCID 0000-0002-3474-1718
Northwestern University · USNational Institute of Biological Sciences, Beijing · CN

Funding

SYNAPTIC CONTROLOF PALLIDAL ACTIVITYP50NS047085 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SURMEIER, DALTON JAMES · 2003 to 2018
$19.2M
General Motor Control Mechanisms and Disease Training ProgramT32NS041234 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI BEVAN, MARK D · 2001 to 2022
$6.0M
Striatopallidal GABAergic Signaling in Mouse Models of Parkinson's DiseaseR01NS069777 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI CHAN, SAVIO · 2010 to 2021
$3.9M
Investigation of Pallidal Neurons in Motor InhibitionR56NS069777 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI CHAN, SAVIO · 2022 to 2022
$536k
Central and Endocrine Stress Pathway Contributions to Alzheimers DiseaseK01AG036738 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI JUSTICE, NICHOLAS J · 2010 to 2013
$502k
NIA NIH HHS K01 AG036738NINDS NIH HHS P50 NS047085NINDS NIH HHS R01 NS069777NINDS NIH HHS R56 NS069777NINDS NIH HHS T32 NS041234
6 · The paper itself

Abstract

unlabelledCompelling evidence demonstrates that the external globus pallidus (GPe) plays a key role in processing sensorimotor information. An anatomical projection from the GPe to the dorsal striatum has been described for decades. However, the cellular target and functional impact of this projection remain unknown. Using cell-specific transgenic mice, modern monosynaptic tracing techniques, and optogenetics-based mapping, we discovered that GPe neurons provide inhibitory inputs to direct and indirect pathway striatal projection neurons (SPNs). Our results indicate that the GPe input to SPNs arises primarily from Npas1-expressing neurons and is strengthened in a chronic Parkinson's disease (PD) model. Alterations of the GPe-SPN input in a PD model argue for the critical position of this connection in regulating basal ganglia motor output and PD symptomatology. Finally, chemogenetic activation of Npas1-expressing GPe neurons suppresses motor output, arguing that strengthening of the GPe-SPN connection is maladaptive and may underlie the hypokinetic symptoms in PD. SIGNIFICANCE STATEMENT: An anatomical projection from the pallidum to the striatum has been described for decades, but little is known about its connectivity pattern. The authors dissect the presynaptic and postsynaptic neurons involved in this projection, and show its cell-specific remodeling and strengthening in parkinsonian mice. Chemogenetic activation of Npas1(+) pallidal neurons that give rise to the principal pallidostriatal projection increases the time that the mice spend motionless. This argues that maladaptive strengthening of this connection underlies the paucity of volitional movements, which is a hallmark of Parkinson's disease.

Indexed as

Synaptic PotentialsAnimalsBasic Helix-Loop-Helix ProteinsGlobus PallidusMiceMice, Inbred C57BLMotor ActivityNerve Tissue ProteinsNeuronsOptogeneticsParkinson DiseaseBasic Helix-Loop-Helix ProteinsNerve Tissue ProteinsNpas1 protein, mouse6-OHDAarkypallidal neuronsextrinsic inhibitionNpas1-Crepallidostriatal projection

Identifiers

PMID27194328
PMCPMC4871984
OpenAlexW2395156094

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.