Evidence map›Paper›PMID 23104117›Full record

ArticleThe Journal of steroid biochemistry and molecular biology2013

Cholecalciferol attenuates perseverative behavior associated with developmental alcohol exposure in rats in a dose-dependent manner.

N M Idrus, J P Happer, J D Thomas

Abstract read
In one paragraph

Article in The Journal of steroid biochemistry and molecular biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.7field-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

7 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Vitamin DBMC medical genetics · 2019
    Article
  3. Effects of prenatal alcohol exposure (PAE): insights into FASD using mouse models of PAE.Biochemistry and cell biology = Biochimie et biologie cellulaire · 2018
    Review
  4. Article
  5. Article
  6. Article
  7. Article
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

3 authors at 1 institution in 1 country.

N M IdrusCenter for Behavioral Teratology, Dept. Psychology, San Diego State University, 6330 Alvarado Court, Ste 100, San Diego, CA 92120, USA. nidrus@projects.sdsu.edu
J P Happer
J D Thomas
San Diego State University · US

Funding

Fetal Alcohol Effects and Choline InterventionR01AA012446 · NIAAA · SAN DIEGO STATE UNIVERSITY · PI THOMAS, JENNIFER D · 2001 to 2015
$3.8M
Fetal Alcohol Effects and Choline InterventionR37AA012446 · NIAAA · SAN DIEGO STATE UNIVERSITY · PI JENNIFER D THOMAS · 2018 to 2026
$3.1M
NIAAA NIH HHS AA12446NIAAA NIH HHS R01 AA012446NIAAA NIH HHS R37 AA012446
6 · The paper itself

Abstract

Alcohol is a known teratogen that is estimated to affect 2-5% of the births in the U.S. Prenatal alcohol exposure can produce physical features such as facial dysmorphology, physiological alterations such as cell loss in the central nervous system (CNS), and behavioral changes that include hyperactivity, cognitive deficits, and motor dysfunction. The range of effects associated with prenatal alcohol exposure is referred to as fetal alcohol spectrum disorders (FASD). Despite preventative measures, some women continue to drink while pregnant. Therefore, identifying interventions that reduce the severity of FASD is critical. This study investigated one such potential intervention, vitamin D3, a nutrient that exerts neuroprotective properties. The present study determined whether cholecalciferol, a common vitamin D3 nutritional supplement, could serve as a means of mitigating alcohol-related learning deficits. Using a rat model of FASD, cholecalciferol was given before, during, and after 3rd trimester equivalent alcohol exposure. Three weeks after cholecalciferol treatment, subjects were tested on a serial spatial discrimination reversal learning task. Animals exposed to ethanol committed significantly more errors compared to controls. Cholecalciferol treatment reduced perseverative behavior that is associated with developmental alcohol exposure in a dose-dependent manner. These data have important implications for the treatment of FASD and suggest that cholecalciferol may reduce some aspects of FASD. This article is part of a Special Issue entitled 'Vitamin D Workshop'.

Indexed as

AnimalsBehavior, AnimalCholecalciferolDiscrimination LearningDisease Models, AnimalDose-Response Relationship, DrugEthanolFemaleFetal Alcohol Spectrum DisordersMaze LearningNeuroprotective AgentsPregnancyPrenatal Exposure Delayed EffectsRatsRats, Sprague-DawleyCholecalciferolEthanolNeuroprotective Agents

Identifiers

PMID23104117
PMCPMC3586753
OpenAlexW1971477726

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.