Evidence map›Paper›PMID 26223289›Full record

ArticleAddiction biology2017

Substance P in the anterior thalamic paraventricular nucleus: promotion of ethanol drinking in response to orexin from the hypothalamus.

Jessica R Barson, Kinning Poon, Hui Tin Ho, Mohammad I Alam, Lilia Sanzalone, Sarah F Leibowitz

Open access · greenAbstract read
In one paragraph

Article in Addiction biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

28 citing papers in PubMed, 41 citations in OpenAlex.

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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.

Jessica R BarsonLaboratory of Behavioral Neurobiology, The Rockefeller University, New York, NY, USA.
Kinning PoonLaboratory of Behavioral Neurobiology, The Rockefeller University, New York, NY, USA.
Hui Tin HoLaboratory of Behavioral Neurobiology, The Rockefeller University, New York, NY, USA.
Mohammad I AlamLaboratory of Behavioral Neurobiology, The Rockefeller University, New York, NY, USA.
Lilia SanzaloneLaboratory of Behavioral Neurobiology, The Rockefeller University, New York, NY, USA.
Sarah F LeibowitzLaboratory of Behavioral Neurobiology, The Rockefeller University, New York, NY, USA.
Rockefeller University · USDrexel University · US

Funding

Transforming Translational Science and Education to Benefit Human HealthUL1TR000043 · NCATS · ROCKEFELLER UNIVERSITY · PI COLLER, BARRY · 2012 to 2015
$26.8M
HYPOTHALAMIC PEPTIDES IN THE CONTROL OF ALCOHOL INTAKER01AA012882 · NIAAA · ROCKEFELLER UNIVERSITY · PI LEIBOWITZ, SARAH F. · 2001 to 2015
$4.0M
Excess ethanol drinking after prenatal exposure to ethanol: chemokine signaling and orexigenic neuropeptidesR01AA024798 · NIAAA · ROCKEFELLER UNIVERSITY · PI LEIBOWITZ, SARAH F. · 2016 to 2020
$1.9M
Paraventricular thalamic nucleus: Role of orexin and opioids in ethanol intakeR00AA021782 · NIAAA · DREXEL UNIVERSITY · PI BARSON, JESSICA ROSE · 2015 to 2017
$747k
Paraventricular thalamic nucleus: Role of orexin and opioids in ethanol intakeK99AA021782 · NIAAA · ROCKEFELLER UNIVERSITY · PI BARSON, JESSICA ROSE · 2013 to 2014
$265k
CXCL12 promotes development of hypothalamic peptide neurons responsive to fatF32DK100058 · NIDDK · ROCKEFELLER UNIVERSITY · PI POON, KINNING · 2013 to 2015
$112k
NCATS NIH HHS UL1 TR000043NIAAA NIH HHS K99 AA021782NIAAA NIH HHS R00 AA021782NIAAA NIH HHS R01 AA012882NIAAA NIH HHS R01 AA024798NIDDK NIH HHS F32 DK100058
6 · The paper itself

Abstract

The paraventricular nucleus of the thalamus (PVT) appears to participate in drug addiction. Recent evidence in rats shows that ethanol drinking is increased by orexin/hypocretin (OX) afferents from the hypothalamus, acting specifically in the anterior (aPVT) rather than posterior (pPVT) PVT subregion. The present study sought to identify neuropeptides transcribed within the PVT, which themselves might contribute to ethanol drinking and possibly mediate the actions of OX. We discovered that substance P (SP) in the aPVT can stimulate intermittent-access ethanol drinking, similar to OX, and that SP receptor [neurokinin 1 receptor/tachykinin receptor 1 (NK1R)] antagonists in this subregion reduce ethanol drinking. As with OX, this effect is site specific, with SP in the pPVT or dorsal third ventricle having no effect on ethanol drinking, and it is behaviorally specific, with SP in the aPVT reducing the drinking of sucrose and stimulating it in the pPVT. A close relationship between SP and OX was demonstrated by a stimulatory effect of local OX injection on SP mRNA and peptide levels, specifically in the aPVT but not pPVT, and a stimulatory effect of OX on SP expression in isolated thalamic neurons, reflecting postsynaptic actions. A functional relationship between OX and SP in the aPVT is suggested by our additional finding that ethanol drinking induced by OX is blocked by a local NK1R antagonist administered at a sub-threshold dose. These results, suggesting that SP in the aPVT mediates the stimulatory effect of OX on ethanol drinking, identify a new role for SP in the control of this behavior.

Indexed as

Behavior, AnimalAnimalsCentral Nervous System DepressantsEthanolHypothalamusMaleModels, AnimalNeurotransmitter AgentsOrexinsRatsRats, Long-EvansSubstance PThalamic NucleiCentral Nervous System DepressantsEthanolNeurotransmitter AgentsOrexinsSubstance PNeurokinin 1 receptorposterior paraventricular thalamustachykinin receptor 1

Identifiers

PMID26223289
PMCPMC4732940
OpenAlexW1584716954

What OpenQuestion holds

Textmetadata
LicenceTDM
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.