Evidence map›Paper›PMID 22957036›Full record

ArticlePloS one2012

Anxiogenic effects of developmental bisphenol A exposure are associated with gene expression changes in the juvenile rat amygdala and mitigated by soy.

Heather B Patisaul, Alana W Sullivan, Meghan E Radford, Deena M Walker, Heather B Adewale, Bozena Winnik, Janis L Coughlin, Brian Buckley, Andrea C Gore

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 1 pooled it
8.5field-weighted citation impact, top 2% 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

61 citing papers in PubMed, 1 synthesis or guideline pooled it, 106 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
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  11. Article
  12. Achieving CLARITY on bisphenol A, brain and behaviour.Journal of neuroendocrinology · 2020
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Neuro-toxic and Reproductive Effects of BPA.Current neuropharmacology · 2019
    Review
  20. Review

1 more citing papers are in PubMed but not listed here.

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 4 institutions in 1 country.

Heather B PatisaulDepartment of Biology, North Carolina State University, Raleigh, North Carolina, United States of America. hbpatisa@ncsu.edu
Alana W Sullivan
Meghan E Radford
Deena M Walker
Heather B Adewale
Bozena Winnik
Janis L Coughlin
Brian Buckley
Andrea C Gore
North Carolina State University · USRutgers, The State University of New Jersey · USThe University of Texas at Austin · USEnvironmental and Occupational Health Sciences Institute · US

Funding

Translational Research Support CoreP30ES005022 · NIEHS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Emily S Barrett · 1988 to 2026
$47.4M
Pilot Project ProgramP30ES007784 · NIEHS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI RICHIE, ELLEN R · 1996 to 2011
$16.4M
TRAINING IN EVIRONMENTAL TOXICOLOGYT32ES007148 · NIEHS · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI Lauren M Aleksunes · 1987 to 2026
$11.4M
Endocrine Disruption of the Hypothalamic Signaling That Regulates PubertyR01ES016001 · NIEHS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI PATISAUL, HEATHER B · 2007 to 2011
$2.0M
Sexually dimorphic effects of endocrine disruptors on brain & behaviorR01ES020662 · NIEHS · UNIVERSITY OF TEXAS AT AUSTIN · PI CREWS, DAVID P, GORE, ANDREA C · 2011 to 2015
$1.8M
Transgenerational epigenetic effects of PCBs on neuroendocrine systemsRC1ES018139 · NIEHS · UNIVERSITY OF TEXAS AT AUSTIN · PI GORE, ANDREA C · 2009 to 2010
$838k
Interaction of BPA and soy isoflavones on sociosexual behaviorR21ES021233 · NIEHS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI PATISAUL, HEATHER B · 2012 to 2013
$435k
Sexually dimorphic effects of endocrine disruptors on brain and behaviorR56ES020662 · NIEHS · UNIVERSITY OF TEXAS AT AUSTIN · PI CREWS, DAVID P, GORE, ANDREA C · 2017 to 2017
$297k
Epigenetic Molecular Mechanisms and Reproductive TransitionsF31AG034813 · NIA · UNIVERSITY OF TEXAS AT AUSTIN · PI WALKER, DEENA M. · 2010 to 2011
$62k
NIA NIH HHS AG034813NIA NIH HHS F31 AG034813NIEHS NIH HHS ES018139NIEHS NIH HHS ES020662NIEHS NIH HHS ES05022NIEHS NIH HHS ES07784NIEHS NIH HHS ES16001NIEHS NIH HHS P30 ES005022NIEHS NIH HHS P30 ES007784NIEHS NIH HHS R01 ES016001NIEHS NIH HHS R01 ES020662NIEHS NIH HHS R21 ES021233NIEHS NIH HHS R56 ES020662NIEHS NIH HHS RC1 ES018139NIEHS NIH HHS T32 ES007148
6 · The paper itself

Abstract

Early life exposure to Bisphenol A (BPA), a component of polycarbonate plastics and epoxy resins, alters sociosexual behavior in numerous species including humans. The present study focused on the ontogeny of these behavioral effects beginning in adolescence and assessed the underlying molecular changes in the amygdala. We also explored the mitigating potential of a soy-rich diet on these endpoints. Wistar rats were exposed to BPA via drinking water (1 mg/L) from gestation through puberty, and reared on a soy-based or soy-free diet. A group exposed to ethinyl estradiol (50 µg/L) and a soy-free diet was used as a positive estrogenic control. Animals were tested as juveniles or adults for anxiety-like and exploratory behavior. Assessment of serum BPA and genistein (GEN), a soy phytoestrogen, confirmed that internal dose was within a human-relevant range. BPA induced anxiogenic behavior in juveniles and loss of sexual dimorphisms in adult exploratory behavior, but only in the animals reared on the soy-free diet. Expression analysis revealed a suite of genes, including a subset known to mediate sociosexual behavior, associated with BPA-induced juvenile anxiety. Notably, expression of estrogen receptor beta (Esr2) and two melanocortin receptors (Mc3r, Mc4r) were downregulated. Collectively, these results show that behavioral impacts of BPA can manifest during adolescence, but wane in adulthood, and may be mitigated by diet. These data also reveal that, because ERβ and melanocortin receptors are crucial to their function, oxytocin/vasopressin signaling pathways, which have previously been linked to human affective disorders, may underlie these behavioral outcomes.

Indexed as

Gene Expression ProfilingAmygdalaAnimalsAnxietyBenzhydryl CompoundsBisphenol A CompoundsEstrogen Receptor betaFemaleGenisteinGlycine maxMaternal ExposurePhenolsPregnancyPregnancy, AnimalRatsRats, WistarBenzhydryl Compoundsbisphenol ABisphenol A CompoundsEstrogen Receptor betaGenisteinPhenolsReceptors, MelanocortinWater

Identifiers

PMID22957036
PMCPMC3434201
OpenAlexW2025397596

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.