Evidence map›Paper›PMID 29075360›Full record

ArticleClinical epigenetics2017

Turnover of histones and histone variants in postnatal rat brain: effects of alcohol exposure.

Nadia Rachdaoui, Ling Li, Belinda Willard, Takhar Kasumov, Stephen Previs, Dipak Sarkar

Open access · goldAbstract read
In one paragraph

Article in Clinical epigenetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.1field-weighted citation impact, top 7% 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

11 citing papers in PubMed, 18 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 4 institutions in 1 country.

Nadia RachdaouiDepartment of Animal Sciences, Rutgers Endocrine Research Program, Rutgers, the State University of New Jersey, 67 Poultry Farm Lane, New Brunswick, NJ 08901 USA.
Ling LiDepartment of Research Core Services, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44106 USA.
Belinda WillardDepartment of Research Core Services, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44106 USA.
Takhar KasumovDepartment of Pharmaceutical Sciences, Northeast Ohio Medical University, Rootstown, OH 44272 USA.
Stephen PrevisCardiometabolic Disease, Merck & Co., Inc, Kenilworth, NJ USA.
Dipak SarkarDepartment of Animal Sciences, Rutgers Endocrine Research Program, Rutgers, the State University of New Jersey, 67 Poultry Farm Lane, New Brunswick, NJ 08901 USA.
Cleveland Clinic Lerner College of Medicine · USRutgers, The State University of New Jersey · USMerck & Co., Inc., Rahway, NJ, USA (United States) · USNortheast Ohio Medical University · US

Funding

ALCOHOL AND HYPERPROLACTINEMIAR01AA011591 · NIAAA · WASHINGTON STATE UNIVERSITY · PI SARKAR, DIPAK KUMAR · 1998 to 2022
$5.0M
Role of Opiates in Alcohol-Induced Neurotoxicity- Diversity supplementR37AA008757 · NIAAA · RUTGERS, THE STATE UNIV OF N.J. · PI SARKAR, DIPAK KUMAR · 2009 to 2018
$4.0M
High-End Instrumentation (HEI) Grant Program (S10)S10OD023436 · OD · CLEVELAND CLINIC LERNER COM-CWRU · PI WILLARD, BELINDA BELLE · 2017 to 2017
$873k
LTQ-Orbitrap Velos instrumentS10RR031537 · NCRR · CLEVELAND CLINIC LERNER COM-CWRU · PI WILLARD, BELINDA BELLE · 2011 to 2011
$600k
Rates of histone turnover and functional significance in fetal alcohol syndromeR21AA024641 · NIAAA · RUTGERS, THE STATE UNIV OF N.J. · PI RACHDAOUI, NADIA, SARKAR, DIPAK KUMAR · 2016 to 2017
$409k
NCRR NIH HHS S10 RR031537NIAAA NIH HHS R01 AA011591NIAAA NIH HHS R21 AA024641NIAAA NIH HHS R37 AA008757NIH HHS S10 OD023436
6 · The paper itself

Abstract

backgroundAlcohol consumption during pregnancy is a significant public health problem and can result in a continuum of adverse outcomes to the fetus known as fetal alcohol spectrum disorders (FASD). Subjects with FASD show significant neurological deficits, ranging from microencephaly, neurobehavioral, and mental health problems to poor social adjustment and stress tolerance. Neurons are particularly sensitive to alcohol exposure. The neurotoxic action of alcohol, i.e., through ROS production, induces DNA damage and neuronal cell death by apoptosis. In addition, epigenetics, including DNA methylation, histone posttranslational modifications (PTMs), and non-coding RNA, play an important role in the neuropathology of FASD. However, little is known about the temporal dynamics and kinetics of histones and their PTMs in FASD.

resultsWe examined the effects of postnatal alcohol exposure (PAE), an animal model of human third-trimester equivalent, on the kinetics of various histone proteins in two distinct brain regions, the frontal cortex, and the hypothalamus, using in vivo

conclusionAlterations in histone turnover might interfere with histone deposition and chromatin stability, resulting in deregulated cell-specific gene expression and therefore contribute to the development of the neurological disorders associated with FASD. Using in vivo

Indexed as

Genetic VariationAcetylationAnimalsCell ProliferationDisease Models, AnimalDNA DamageEpigenesis, GeneticFemaleFetal Alcohol Spectrum DisordersHistonesHumansPregnancyProtein Processing, Post-TranslationalProteomicsRatsRats, Sprague-DawleyHistones2H2O-labelingBrainHistoneMass spectrometryPostnatal alcohol exposurePost-translational modificationsTurnover

Identifiers

PMID29075360
PMCPMC5654083
OpenAlexW2767069031

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.