Evidence map›Paper›PMID 29969146›Full record

ArticleAlcoholism, clinical and experimental research2018

Pituitary Adenylate Cyclase-Activating Polypeptide-27 (PACAP-27) in the Thalamic Paraventricular Nucleus Is Stimulated by Ethanol Drinking.

Anuranita Gupta, Andrew T Gargiulo, Genevieve R Curtis, Preeti S Badve, Surya Pandey, Jessica R Barson

Abstract read
In one paragraph

Article in Alcoholism, clinical and experimental research, 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
1.9field-weighted citation impact, top 15% 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, 31 citations in OpenAlex.

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  12. Pituitary adenylate cyclase-activating polypeptide (PACAP) modulates dependence-induced alcohol drinking and anxiety-like behavior in male rats.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 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

6 authors at 1 institution in 1 country.

Anuranita GuptaDepartment of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, Pennsylvania.
Andrew T GargiuloDepartment of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, Pennsylvania.
Genevieve R CurtisDepartment of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, Pennsylvania.
Preeti S BadveDepartment of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, Pennsylvania.
Surya PandeyDepartment of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, Pennsylvania.
Jessica R BarsonDepartment of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, Pennsylvania.ORCID 0000-0001-7227-5730
Drexel University · US

Funding

Paraventricular thalamic nucleus: Role of orexin and opioids in ethanol intakeR00AA021782 · NIAAA · DREXEL UNIVERSITY · PI BARSON, JESSICA ROSE · 2015 to 2017
$747k
NIAAA NIH HHS R00 AA021782
6 · The paper itself

Abstract

backgroundThe paraventricular nucleus of the thalamus (PVT) is a limbic brain structure that affects ethanol (EtOH) drinking, but the neurochemicals transcribed in this nucleus that may participate in this behavior have yet to be fully characterized. The neuropeptide, pituitary adenylate cyclase-activating polypeptide (PACAP), is known to be transcribed in other limbic areas and to be involved in many of the same behaviors as the PVT itself, possibly including EtOH drinking. It exists in 2 isoforms, PACAP-38 and PACAP-27, with the former expressed at higher levels in most brain regions. The purpose of this study was to characterize PACAP in the PVT and to assess its response to EtOH drinking.

methodsFirst, EtOH-naïve, Sprague Dawley rats were examined using quantitative real-time polymerase chain reaction (qPCR) and immunohistochemistry, to characterize PACAP mRNA and peptide throughout the rostrocaudal axis of the PVT. Next, EtOH-naïve, vGLUT2-GFP transgenic mice were examined using immunohistochemistry, to identify the neurochemical phenotype of the PACAPergic cells in the PVT. Finally, Long Evans rats were trained to drink 20% EtOH under the intermittent-access paradigm and then examined with PCR and immunohistochemistry, to determine the effects of EtOH on endogenous PACAP in the PVT.

resultsGene expression of PACAP was detected across the entire PVT, denser in the posterior than the anterior portion of this nucleus. The protein isoform, PACAP-27, was present in a high percentage of cell bodies in the PVT, again particularly in the posterior portion, while PACAP-38 was instead dense in fibers. All PACAP-27

conclusionsThis study characterizes the PVT neuropeptide, PACAP, and its understudied protein isoform, PACAP-27, and demonstrates that it is involved in pharmacologically relevant EtOH drinking. This indicates that PACAP-27 should be further investigated for its possible role in EtOH drinking.

Indexed as

Alcohol DrinkingAnimalsMaleMiceMice, Inbred C57BLMice, TransgenicMidline Thalamic NucleiPituitary Adenylate Cyclase-Activating PolypeptideRatsRats, Sprague-DawleyPituitary Adenylate Cyclase-Activating PolypeptideAnterior Paraventricular Nucleus of the ThalamusIntermittent AccessPACAP-38Pituitary Adenylate Cyclase-Activating PolypeptidePosterior Paraventricular Nucleus of the Thalamus

Identifiers

PMID29969146
PMCPMC6120804
OpenAlexW2809999992

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.