Evidence map›Paper›PMID 41157203›Full record

ArticleLife (Basel, Switzerland)2025

Docosahexaenoic Acid Increases the Pro-Resolving Brain Lipid Mediators of Inflammation in Rat Pups Prenatally Exposed to Alcohol.

Enrique M Ostrea, Deepak Yadav, Charlie T Cheng, Esther D Kisseih, Krishna R Maddipati, Ronald L Thomas

Abstract read
In one paragraph

Article in Life (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

6 authors.

Enrique M OstreaDivision of Neonatal-Perinatal Medicine, Department of Pediatrics, Hutzel Women's Hospital and Children's Hospital of Michigan, Wayne State University School of Medicine, 3901 Beaubien St., Detroit, MI 48201, USA.ORCID 0000-0002-5516-7102
Deepak YadavDivision of Neonatal-Perinatal Medicine, Department of Pediatrics, Hutzel Women's Hospital and Children's Hospital of Michigan, Wayne State University School of Medicine, 3901 Beaubien St., Detroit, MI 48201, USA.ORCID 0000-0003-2571-3958
Charlie T ChengDivision of Neonatal-Perinatal Medicine, Department of Pediatrics, Hutzel Women's Hospital and Children's Hospital of Michigan, Wayne State University School of Medicine, 3901 Beaubien St., Detroit, MI 48201, USA.
Esther D KisseihDivision of Neonatal-Perinatal Medicine, Department of Pediatrics, Hutzel Women's Hospital and Children's Hospital of Michigan, Wayne State University School of Medicine, 3901 Beaubien St., Detroit, MI 48201, USA.
Krishna R MaddipatiBioactive Lipids Research Program, Wayne State University, Detroit, MI 48202, USA.ORCID 0000-0003-1445-791X
Ronald L ThomasDivision of Neonatal-Perinatal Medicine, Department of Pediatrics, Hutzel Women's Hospital and Children's Hospital of Michigan, Wayne State University School of Medicine, 3901 Beaubien St., Detroit, MI 48201, USA.

Funding

Sarnaik Endowment Research Foundation of the Children's Research Center of the Children's Hospital of Michigan. Detroit, Michigan. 2018-01
6 · The paper itself

Abstract

Fetal alcohol spectrum disorder (FASD/FAS) is a chronic inflammatory process of the fetal brain induced by alcohol and mediated by pro-inflammatory (PILM) and pro-resolving (PRLM) lipid mediators of inflammation. DHA (docosahexaenoic acid) is an essential precursor of PRLM. A study examining the response of lipid mediators of inflammation to alcohol insult and DHA supplementation can provide vital information on the pathogenesis of FASD/FAS and the potential ameliorative role of DHA. Four groups of timed pregnant rats were studied: control, low-dose (1.6 g/kg/day) and high-dose (2.4 g/kg/day) alcohol, and high-dose alcohol (2.4 g/kg/day) + DHA (1250 mg/kg/day). The pups were delivered on day 20, and their whole brain was examined for lipid mediators by liquid chromatography mass spectroscopy. The following biomarkers of brain lipid mediators were studied, namely, PILM (LTB4, PGE2, PGF2α, TXB2) and PRLM (LXA5, 4-HDoHE, 17-HDoHE, and MaR1n-3, DPA). The brain PILM and PRLM concentrations decreased significantly (

Indexed as

alcoholic pregnant ratsdocosahexaenoic acidinflammationnewborn rat pupspro-inflammatory brain lipid mediatorpro-resolving brain lipid mediators

Identifiers

PMID41157203
PMCPMC12564984

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Registered trials

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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.