Evidence map›Paper›PMID 28575455›Full record

ArticleThe international journal of neuropsychopharmacology2017

Adolescent Alcohol Exposure-Induced Changes in Alpha-Melanocyte Stimulating Hormone and Neuropeptide Y Pathways via Histone Acetylation in the Brain During Adulthood.

Dadasaheb M Kokare, Evan J Kyzar, Huaibo Zhang, Amul J Sakharkar, Subhash C Pandey

Open access · goldAbstract read
In one paragraph

Article in The international journal of neuropsychopharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

32 citing papers in PubMed, 55 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

5 authors at 1 institution in 1 country.

Dadasaheb M KokareCenter for Alcohol Research in Epigenetics, Department of Psychiatry, and Department of Anatomy and Cell Biology, University of Illinois at Chicago, Chicago; Jesse Brown Veterans Affairs Medical Center, Chicago, Illinois.
Evan J KyzarCenter for Alcohol Research in Epigenetics, Department of Psychiatry, and Department of Anatomy and Cell Biology, University of Illinois at Chicago, Chicago; Jesse Brown Veterans Affairs Medical Center, Chicago, Illinois.
Huaibo ZhangCenter for Alcohol Research in Epigenetics, Department of Psychiatry, and Department of Anatomy and Cell Biology, University of Illinois at Chicago, Chicago; Jesse Brown Veterans Affairs Medical Center, Chicago, Illinois.
Amul J SakharkarCenter for Alcohol Research in Epigenetics, Department of Psychiatry, and Department of Anatomy and Cell Biology, University of Illinois at Chicago, Chicago; Jesse Brown Veterans Affairs Medical Center, Chicago, Illinois.
Subhash C PandeyCenter for Alcohol Research in Epigenetics, Department of Psychiatry, and Department of Anatomy and Cell Biology, University of Illinois at Chicago, Chicago; Jesse Brown Veterans Affairs Medical Center, Chicago, Illinois.
University of Illinois Chicago · US

Funding

Pilot Project Program P50AA022538 · NIAAA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI DENNIS R GRAYSON · 2015 to 2026
$21.3M
Role of AIE in Epigenetic and Behavioral Changes at AdulthoodU01AA019971 · NIAAA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI PANDEY, SUBHASH C. · 2010 to 2024
$5.6M
2/2 NADIA U24 Epigenetic/Molecular CoreU24AA024605 · NIAAA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI PANDEY, SUBHASH C. · 2015 to 2024
$3.6M
Signaling Mechanisms in Alcohol Drinking BehaviorsR01AA010005 · NIAAA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI PANDEY, SUBHASH C. · 2001 to 2017
$3.0M
Brain histone methylation mechanisms in adulthood after adolescent alcohol exposureF30AA024948 · NIAAA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI KYZAR, EVAN · 2016 to 2019
$197k
Cellular Signaling in AlcoholismI01BX000143 · VA · JESSE BROWN VA MEDICAL CENTER · PI PANDEY, SUBHASH C. · 2011 to 2014
–
BLRD VA I01 BX000143NIAAA NIH HHS F30 AA024948NIAAA NIH HHS P50 AA022538NIAAA NIH HHS R01 AA010005NIAAA NIH HHS U01 AA019971NIAAA NIH HHS U24 AA024605
6 · The paper itself

Abstract

Background: Adolescent intermittent ethanol exposure causes long-lasting alterations in brain epigenetic mechanisms. Melanocortin and neuropeptide Y signaling interact and are affected by ethanol exposure in the brain. Here, the persistent effects of adolescent intermittent ethanol on alpha-melanocyte stimulating hormone, melanocortin 4 receptor, and neuropeptide Y expression and their regulation by histone acetylation mechanisms were investigated in adulthood. Methods: Male rats were exposed to adolescent intermittent ethanol (2 g/kg, i.p.) or volume-matched adolescent intermittent saline from postnatal days 28 to 41 and allowed to grow to postnatal day 92. Anxiety-like behaviors were measured by the elevated plus-maze test. Brain regions from adult rats were used to examine changes in alpha-melanocyte stimulating hormone, melanocortin 4 receptor, and neuropeptide Y expression and the histone acetylation status of their promoters. Results: Adolescent intermittent ethanol-exposed adult rats displayed anxiety-like behaviors and showed increased pro-opiomelanocortin mRNA levels in the hypothalamus and increased melanocortin 4 receptor mRNA levels in both the amygdala and hypothalamus compared with adolescent intermittent saline-exposed adult rats. The alpha-Melanocyte stimulating hormone and melanocortin 4 receptor protein levels were increased in the central and medial nucleus of the amygdala, paraventricular nucleus, and arcuate nucleus of the hypothalamus in adolescent intermittent ethanol-exposed compared with adolescent intermittent saline-exposed adult rats. Neuropeptide Y protein levels were decreased in the central and medial nucleus of the amygdala of adolescent intermittent ethanol-exposed compared with adolescent intermittent saline-exposed adult rats. Histone H3K9/14 acetylation was decreased in the neuropeptide Y promoter in the amygdala but increased in the melanocortin 4 receptor gene promoter in the amygdala and the melanocortin 4 receptor and pro-opiomelanocortin promoters in the hypothalamus of adolescent intermittent ethanol-exposed adult rats compared with controls. Conclusions: Increased melanocortin and decreased neuropeptide Y activity due to changes in histone acetylation in emotional brain circuitry may play a role in adolescent intermittent ethanol-induced anxiety phenotypes in adulthood.

Indexed as

BrainAcetylationalpha-MSHAnimalsAnxietyCentral Nervous System DepressantsChromatin ImmunoprecipitationEthanolFemaleGene Expression Regulation, DevelopmentalHistonesHumansMaleNeuropeptide YPregnancyPro-Opiomelanocortinalpha-MSHCentral Nervous System DepressantsEthanolHistonesNeuropeptide YPro-OpiomelanocortinReceptor, Melanocortin, Type 4RNA, Messengeradolescencealcoholalpha-melanocyte stimulating hormonehistone H3 acetylationmelanocortin 4 receptorneuropeptide Y

Identifiers

PMID28575455
PMCPMC5581492
OpenAlexW2619598574

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.