Literature DB >> 15811588

Chronic exposure to low doses bisphenol A interferes with pair-bonding and exploration in female Mongolian gerbils.

M Razzoli1, P Valsecchi, P Palanza.   

Abstract

Estrogenic endocrine disruptors, synthetic or naturally occurring substances found in the environment, can interfere with the vertebrate endocrine system and, mimicking estrogens, interact with the neuroendocrine substrates of behavior. Since species vary in their sensitivity to steroids, it is of great interest to widen the range of species included in the researches on neurobehavioral effects of estrogenic endocrine disruptors. We examined socio-sexual and exploratory behavior of Mongolian gerbil females (Meriones unguiculatus), a monogamous rodent, in response to chronic exposure to the estrogenic endocrine disruptor bisphenol A. Paired females were daily administered with one of the following treatments: bisphenol A (2 or 20 microg/kg body weight/day); 17alpha-ethynil estradiol (0.04 microg/kg body weight/day 17alphaE); oil (vehicle). Females were treated for 3 weeks after pairing. Starting on day of pairing, social interactions within pairs were daily recorded. Three weeks after pairing, females were individually tested in a free exploratory paradigm. Bisphenol A and 17alphaE affected male-female social interactions by increasing social investigation. Bisphenol A reduced several exploratory parameters, indicating a decreased exploratory propensity of females. These results highlight the sensitivity of adult female gerbils to bisphenol A during the hormonally sensitive period of pair formation, also considering that the bisphenol A doses tested are well below the suggested human tolerable daily intake.

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Year:  2004        PMID: 15811588     DOI: 10.1016/j.brainresbull.2004.11.013

Source DB:  PubMed          Journal:  Brain Res Bull        ISSN: 0361-9230            Impact factor:   4.077


  7 in total

Review 1.  Hormones and endocrine-disrupting chemicals: low-dose effects and nonmonotonic dose responses.

Authors:  Laura N Vandenberg; Theo Colborn; Tyrone B Hayes; Jerrold J Heindel; David R Jacobs; Duk-Hee Lee; Toshi Shioda; Ana M Soto; Frederick S vom Saal; Wade V Welshons; R Thomas Zoeller; John Peterson Myers
Journal:  Endocr Rev       Date:  2012-03-14       Impact factor: 19.871

Review 2.  In vivo effects of bisphenol A in laboratory rodent studies.

Authors:  Catherine A Richter; Linda S Birnbaum; Francesca Farabollini; Retha R Newbold; Beverly S Rubin; Chris E Talsness; John G Vandenbergh; Debby R Walser-Kuntz; Frederick S vom Saal
Journal:  Reprod Toxicol       Date:  2007-06-26       Impact factor: 3.143

Review 3.  Bisphenol A and phthalate endocrine disruption of parental and social behaviors.

Authors:  Cheryl S Rosenfeld
Journal:  Front Neurosci       Date:  2015-03-03       Impact factor: 4.677

4.  Effects of developmental bisphenol A exposure on reproductive-related behaviors in California mice (Peromyscus californicus): a monogamous animal model.

Authors:  Scott A Williams; Eldin Jasarevic; Gregory M Vandas; Denise A Warzak; David C Geary; Mark R Ellersieck; R Michael Roberts; Cheryl S Rosenfeld
Journal:  PLoS One       Date:  2013-02-06       Impact factor: 3.240

5.  Bisphenol A induces hepatotoxicity through oxidative stress in rat model.

Authors:  Zeinab K Hassan; Mai A Elobeid; Promy Virk; Sawsan A Omer; Maha ElAmin; Maha H Daghestani; Ebtisam M AlOlayan
Journal:  Oxid Med Cell Longev       Date:  2012-07-24       Impact factor: 6.543

Review 6.  Effects of bisphenol-A and other endocrine disruptors compared with abnormalities of schizophrenia: an endocrine-disruption theory of schizophrenia.

Authors:  James S Brown
Journal:  Schizophr Bull       Date:  2008-01-31       Impact factor: 9.306

7.  Vitamin D mitigates adult onset diseases in male and female mice induced by early-life exposure to endocrine disruptor BPA.

Authors:  Mohamed A Al-Griw; Zohour M Marwan; Ismail M Hdud; Taher Shaibi
Journal:  Open Vet J       Date:  2021-08-12
  7 in total

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