Evidence map›Paper›PMID 36829814›Full record

ArticleAntioxidants (Basel, Switzerland)2023

Impact of Prenatal Alcohol Exposure on the Development and Myocardium of Adult Mice: Morphometric Changes, Transcriptional Modulation of Genes Related to Cardiac Dysfunction, and Antioxidant Cardioprotection.

Allan Luís Barboza Atum, Leonardo Paroche de Matos, Bruna Calixto de Jesus, Guilherme Rabelo Nasuk, Gabriel Almeida da Silva, Caio Perez Gomes, João Bosco Pesquero, Stella Regina Zamuner, José Antônio Silva Júnior

Open access · goldAbstract read
In one paragraph

Article in Antioxidants (Basel, Switzerland), 2023. 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
6.4field-weighted citation impact, top 4% 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, 11 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

9 authors at 2 institutions in 1 country.

Allan Luís Barboza AtumMedicine Department, Universidade Nove de Julho-UNINOVE, Rua Vergueiro 249, São Paulo 01504-001, SP, Brazil.ORCID 0000-0003-0980-4390
Leonardo Paroche de MatosMedicine Department, Universidade Nove de Julho-UNINOVE, Rua Vergueiro 249, São Paulo 01504-001, SP, Brazil.
Bruna Calixto de JesusMedicine Department, Universidade Nove de Julho-UNINOVE, Rua Vergueiro 249, São Paulo 01504-001, SP, Brazil.
Guilherme Rabelo NasukMedicine Department, Universidade Nove de Julho-UNINOVE, Rua Vergueiro 249, São Paulo 01504-001, SP, Brazil.
Gabriel Almeida da SilvaMedicine Department, Universidade Nove de Julho-UNINOVE, Rua Vergueiro 249, São Paulo 01504-001, SP, Brazil.
Caio Perez GomesBiophysics Department, Universidade Federal de São Paulo, Rua Pedro de Toledo 669, São Paulo 04039-032, SP, Brazil.ORCID 0000-0002-6553-7701
João Bosco PesqueroBiophysics Department, Universidade Federal de São Paulo, Rua Pedro de Toledo 669, São Paulo 04039-032, SP, Brazil.
Stella Regina ZamunerMedicine Department, Universidade Nove de Julho-UNINOVE, Rua Vergueiro 249, São Paulo 01504-001, SP, Brazil.ORCID 0000-0002-4694-7617
José Antônio Silva JúniorMedicine Department, Universidade Nove de Julho-UNINOVE, Rua Vergueiro 249, São Paulo 01504-001, SP, Brazil.ORCID 0000-0001-6904-9185
Universidade Nove de Julho · BRUniversidade Federal de São Paulo · BR

Funding

National Council for Scientific and Technological Development 312381/2021-2
6 · The paper itself

Abstract

The impact of prenatal alcohol exposure (PAE) varies considerably between individuals, leading to morphological and genetic changes. However, minor changes usually go undetected in PAE children. We investigated PAE's effects on gene transcription of genes related to cardiac dysfunction signaling in mouse myocardium and morphological changes. C57Bl/6 mice were subjected to a 10% PAE protocol. In postnatal days 2 and 60 (PN2 and PN60), morphometric measurements in the offspring were performed. Ventricular samples of the heart were collected in PN60 from male offspring for quantification of mRNA expression of 47 genes of nine myocardial signal transduction pathways related to cardiovascular dysfunction. Animals from the PAE group presented low birth weight than the Control group, but the differences were abolished in adult mice. In contrast, the mice's size was similar in PN2; however, PAE mice were oversized at PN60 compared with the Control group. Cardiac and ventricular indexes were increased in PAE mice. PAE modulated the mRNA expression of 43 genes, especially increasing the expressions of genes essential for maladaptive tissue remodeling. PAE animals presented increased antioxidant enzyme activities in the myocardium. In summary, PAE animals presented morphometric changes, transcription of cardiac dysfunction-related genes, and increased antioxidant protection in the myocardium.

Indexed as

cardiac dysfunctionmyocardiumoxidative stressprenatal alcohol exposuresignal transduction

Identifiers

PMID36829814
PMCPMC9952294
OpenAlexW4317738574

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.