Evidence map›Paper›PMID 30209240›Full record

ArticleThe EMBO journal2018

Hypothalamic CNTF volume transmission shapes cortical noradrenergic excitability upon acute stress.

Alán Alpár, Péter Zahola, János Hanics, Zsófia Hevesi, Solomiia Korchynska, Marco Benevento, Christian Pifl, Gergely Zachar, Jessica Perugini, Ilenia Severi and 19 more

Open access · hybridAbstract read
In one paragraph

Article in The EMBO journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

21 citing papers in PubMed, 47 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

29 authors at 9 institutions in 6 countries.

Alán AlpárSE NAP Research Group of Experimental Neuroanatomy and Developmental Biology, Semmelweis University, Budapest, Hungary alpar.alan@med.semmelweis-univ.hu tibor.harkany@meduniwien.ac.at.
Péter ZaholaSE NAP Research Group of Experimental Neuroanatomy and Developmental Biology, Semmelweis University, Budapest, Hungary.
János HanicsSE NAP Research Group of Experimental Neuroanatomy and Developmental Biology, Semmelweis University, Budapest, Hungary.
Zsófia HevesiSE NAP Research Group of Experimental Neuroanatomy and Developmental Biology, Semmelweis University, Budapest, Hungary.
Solomiia KorchynskaDepartment of Molecular Neurosciences, Center for Brain Research, Medical University of Vienna, Vienna, Austria.
Marco BeneventoDepartment of Molecular Neurosciences, Center for Brain Research, Medical University of Vienna, Vienna, Austria.
Christian PiflDepartment of Molecular Neurosciences, Center for Brain Research, Medical University of Vienna, Vienna, Austria.
Gergely ZacharDepartment of Anatomy, Histology, and Embryology, Semmelweis University, Budapest, Hungary.
Jessica PeruginiSection of Neuroscience and Cell Biology, Department of Experimental and Clinical Medicine, Marche Polytechnic University, Ancona, Italy.
Ilenia SeveriSection of Neuroscience and Cell Biology, Department of Experimental and Clinical Medicine, Marche Polytechnic University, Ancona, Italy.
Patrick LeitgebDepartment of Molecular Neurosciences, Center for Brain Research, Medical University of Vienna, Vienna, Austria.
Joanne BakkerDepartment of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Andras G MiklosiDepartment of Molecular Neurosciences, Center for Brain Research, Medical University of Vienna, Vienna, Austria.
Evgenii TretiakovImmanuel Kant Baltic Federal University, Kaliningrad, Russia.
Erik KeimpemaDepartment of Molecular Neurosciences, Center for Brain Research, Medical University of Vienna, Vienna, Austria.
Gloria ArqueDepartment of Molecular Neurosciences, Center for Brain Research, Medical University of Vienna, Vienna, Austria.
Ramon O TasanDepartment of Pharmacology, Medical University Innsbruck, Innsbruck, Austria.
Günther SperkDepartment of Pharmacology, Medical University Innsbruck, Innsbruck, Austria.
Katarzyna MalenczykDepartment of Molecular Neurosciences, Center for Brain Research, Medical University of Vienna, Vienna, Austria.
Zoltán MátéInstitute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, Hungary.
Ferenc ErdélyiInstitute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, Hungary.
Gábor SzabóInstitute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, Hungary.
Gert LubecParacelsus Medical University, Salzburg, Austria.
Miklós PalkovitsDepartment of Anatomy, Histology, and Embryology, Semmelweis University, Budapest, Hungary.
Antonio GiordanoSection of Neuroscience and Cell Biology, Department of Experimental and Clinical Medicine, Marche Polytechnic University, Ancona, Italy.
Tomas Gm HökfeltDepartment of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Roman A RomanovDepartment of Molecular Neurosciences, Center for Brain Research, Medical University of Vienna, Vienna, Austria.
Tamas L HorvathProgram in Integrative Cell Signaling and Neurobiology of Metabolism, Departments of Comparative Medicine and Neuroscience, Kavli Institute for Neuroscience, Yale University School of Medicine, New Haven, CT, USA.
Tibor HarkanyDepartment of Molecular Neurosciences, Center for Brain Research, Medical University of Vienna, Vienna, Austria alpar.alan@med.semmelweis-univ.hu tibor.harkany@meduniwien.ac.at.ORCID 0000-0002-6637-5900
Medical University of Vienna · ATSemmelweis University · HUMarche Polytechnic University · ITHUN-REN Institute of Experimental Medicine · HUImmanuel Kant Baltic Federal University · RUInnsbruck Medical University · ATKarolinska Institutet · SEParacelsus Medical University · ATYale University · US

Funding

The role of AgRP/Auga-ALK pathway in FGF21's brain action on agingP01AG051459 · NIA · YALE UNIVERSITY · PI VISHWA DEEP DIXIT · 2016 to 2026
$25.7M
Austrian Science Fund FWF DOC 33Austrian Science Fund FWF P 29952European Research Council 695136NIA NIH HHS P01 AG051459
6 · The paper itself

Abstract

Stress-induced cortical alertness is maintained by a heightened excitability of noradrenergic neurons innervating, notably, the prefrontal cortex. However, neither the signaling axis linking hypothalamic activation to delayed and lasting noradrenergic excitability nor the molecular cascade gating noradrenaline synthesis is defined. Here, we show that hypothalamic corticotropin-releasing hormone-releasing neurons innervate ependymal cells of the 3

Indexed as

Stress, PhysiologicalAdrenergic NeuronsAnimalsCiliary Neurotrophic FactorHypothalamusLocus CoeruleusMiceMice, KnockoutRatsCiliary Neurotrophic FactorCa2+‐sensor proteinhypothalamus–pituitary–adrenal axisneurotrophinpost‐traumatic stress disorderprefrontal cortex

Identifiers

PMID30209240
PMCPMC6213283
OpenAlexW2890676872

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.