Evidence map›Paper›PMID 35143549›Full record

ArticlePloS one2022

Transgenerational inheritance of fetal alcohol effects on proopiomelanocortin gene expression and methylation, cortisol response to stress, and anxiety-like behaviors in offspring for three generations in rats: Evidence for male germline transmission.

Omkaram Gangisetty, Shaista Chaudhary, Ajay Palagani, Dipak K Sarkar

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. 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
6.1field-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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Epigenetics of Trauma Transmission and Fetal Alcohol Spectrum Disorder: What Does the Evidence Support?International journal of environmental research and public health · 2023
    Review
  8. Article
  9. Fetal alcohol spectrum disorders.Nature reviews. Disease primers · 2023
    Review
  10. Review
  11. 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

4 authors at 1 institution in 1 country.

Omkaram GangisettyRutgers Endocrine Research Program, Department of Animal Sciences, Rutgers University, New Brunswick, New Jersey, United States of America.
Shaista ChaudharyRutgers Endocrine Research Program, Department of Animal Sciences, Rutgers University, New Brunswick, New Jersey, United States of America.
Ajay PalaganiRutgers Endocrine Research Program, Department of Animal Sciences, Rutgers University, New Brunswick, New Jersey, United States of America.
Dipak K SarkarRutgers Endocrine Research Program, Department of Animal Sciences, Rutgers University, New Brunswick, New Jersey, United States of America.ORCID 0000-0003-3237-9871
Rutgers, The State University of New Jersey · US

Funding

Role of SRY in transgenerational transmission of alcohol epigenetic marks on proopiomelanocortin geneR01AA025359 · NIAAA · RUTGERS, THE STATE UNIV OF N.J. · PI SARKAR, DIPAK KUMAR · 2017 to 2021
$1.7M
NIAAA NIH HHS R01 AA025359
6 · The paper itself

Abstract

Previously it has been shown that fetal alcohol exposure increases the stress response partly due to lowering stress regulatory proopiomelanocortin (Pomc) gene expression in the hypothalamus via epigenetic mechanisms for multiple generations in mixed-breed rats. In this study we assess the induction of heritable epigenetic changes of Pomc-related variants by fetal alcohol exposure in isogenic Fischer 344 rats. Using transgenerational breeding models and fetal alcohol exposure procedures, we determined changes in hypothalamic Pomc gene expression and its methylation levels, plasma corticosterone hormone response to restraint stress, and anxiety-like behaviors using elevated plus maze tests in fetal alcohol-exposed offspring for multiple generations in isogenic Fischer rats. Fetal alcohol-exposed male and female rat offspring showed significant deficits in POMC neuronal functions with increased Pomc gene methylation and reduced expression. These changes in POMC neuronal functions were associated with increased plasma corticosterone response to restraint stress and increased anxiety-like behavior. These effects of fetal alcohol exposure persisted in the F1, F2, and F3 progeny of the male germline but not of the female germline. These data suggest that fetal alcohol exposure induces heritable changes in Pomc-related variants involving stress hyperresponsiveness and anxiety-like behaviors which perpetuate into subsequent generations through the male germline via epigenetic modifications.

Indexed as

AnxietyDNA MethylationPrenatal Exposure Delayed EffectsPro-OpiomelanocortinAnimalsCorticosteroneEpigenesis, GeneticEthanolFemaleFetal Alcohol Spectrum DisordersGerm CellsHydrocortisoneHypothalamusMalePregnancyRatsCorticosteroneEthanolHydrocortisonePro-Opiomelanocortin

Identifiers

PMID35143549
PMCPMC8830645
OpenAlexW4211070872

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.