Evidence map›Paper›PMID 24975924›Full record

ArticleSynapse (New York, N.Y.)2014

Adolescent bisphenol-A exposure decreases dendritic spine density: role of sex and age.

Rachel E Bowman, Victoria Luine, Hameda Khandaker, Joseph J Villafane, Maya Frankfurt

Open access · greenAbstract read
In one paragraph

Article in Synapse (New York, N.Y.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 8% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Sex differences in cognition following variations in endocrine status.Learning & memory (Cold Spring Harbor, N.Y.) · 2022
    Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Bisphenol A Impairs Synaptic Plasticity by Both Pre- and Postsynaptic Mechanisms.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2017
    Article
  14. Effects of Water Bottle Materials and Filtration on Bisphenol A Content in Laboratory Animal Drinking Water.Journal of the American Association for Laboratory Animal Science : JAALAS · 2017
    Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. 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

5 authors at 3 institutions in 1 country.

Rachel E BowmanDepartment of Psychology, Sacred Heart University, Fairfield, Connecticut, 06825.
Victoria Luine
Hameda Khandaker
Joseph J Villafane
Maya Frankfurt
Hunter College · USSacred Heart University · USHofstra University · US

Funding

BP-ENDURE at Hunter and NYUR25NS080686 · NINDS · HUNTER COLLEGE · PI Nesha Star Burghardt, GLENN E SCHAFE · 2012 to 2026
$9.2M
Neurobiology of Addiction &Impulsive BehaviorR24DA012136 · NIDA · HUNTER COLLEGE · PI QUINONES-JENAB, VANYA · 1999 to 2016
$5.2M
NIDA NIH HHS R24 DA012136NINDS NIH HHS R25 NS080686NINDS NIH HHS R25-NS080686
6 · The paper itself

Abstract

Bisphenol-A (BPA), a common environmental endocrine disruptor, modulates estrogenic, androgenic, and antiandrogenic effects throughout the lifespan. We recently showed that low dose BPA exposure during adolescence increases anxiety and impairs spatial memory independent of sex. In this study, six week old Sprague Dawley rats (n=24 males, n=24 females) received daily subcutaneous injections (40 µg/kg bodyweight) of BPA or vehicle for one week. Serum corticosterone levels in response to a 1 h restraint stress and spine density were examined at age 7 (cohort 1) and 11 (cohort 2) weeks. Adolescent BPA exposure did not alter stress dependent corticosterone responses but decreased spine density on apical and basal dendrites of pyramidal cells in the medial prefrontal cortex (mPFC) and hippocampal CA1 region (CA1). Sex differences in spine density were observed on basal dendrites of the mPFC and CA1 with females having greater spine density than males. This sex difference was further augmented by both age and treatment, with results indicating that BPA-dependent decreases in spine density were more pronounced in males than females on mPFC basal dendrites. Importantly, the robust neuronal alterations were observed in animals exposed to BPA levels below the current U.S.E.P.A. recommended safe daily limit. These results are the first demonstrating that BPA given during adolescence leads to enduring effects on neural morphology at adulthood. Given that humans are routinely exposed to low levels of BPA through a variety of sources, the decreased spine density reported in both male and female rats after BPA exposure warrants further investigation.

Indexed as

Age FactorsAnimalsBenzhydryl CompoundsBisphenol A CompoundsCA1 Region, HippocampalCorticosteroneDendritic SpinesEndocrine DisruptorsFemaleMalePhenolsPrefrontal CortexPyramidal CellsRatsRats, Sprague-DawleySex FactorsBenzhydryl Compoundsbisphenol ABisphenol A CompoundsCorticosteroneEndocrine DisruptorsPhenolscorticosteronehippocampusmedial prefrontal cortex

Identifiers

PMID24975924
PMCPMC6112112
OpenAlexW1483632196

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.