Literature DB >> 18368283

Behavioural characterisation of rats exposed neonatally to bisphenol-A: responses to a novel environment and to methylphenidate challenge in a putative model of attention-deficit hyperactivity disorder.

Motori Kiguchi1, Satoshi Fujita, Hidero Oki, Noriyoshi Shimizu, Alexander R Cools, Noriaki Koshikawa.   

Abstract

Neonatal exposure of rats to bisphenol-A, an endocrine disruptor, has recently been proposed as a possible animal model of attention-deficit hyperactivity disorder (ADHD), because such rats exhibit motor hyperactivity. To strengthen the face validity of this animal model, the present study replicated the original experiments and additionally analysed both changes in habituation to a novel environment and behavioural responses to methylphenidate, the two phenomena known to be altered in ADHD. Single intracisternal administration of bisphenol-A (20 and 40 microg) into 5-day-old male Wistar rats impaired habituation to a novel environment in the light, but not the dark, phase at 4 weeks of age. Thus, habituation as assessed by time-dependent decrease of locomotor activity, rearing, sniffing and grooming was significantly reduced in bisphenol-A-pretreated rats. Methylphenidate (1 and 3 mg/kg, i.p.) dose-dependently enhanced locomotor activity in both vehicle-pretreated and bisphenol-A-pretreated rats during both the dark and the light phases. Thus, the effects of methylphenidate did not differ between bisphenol-A-pretreated and vehicle-pretreated rats. Apart from a slight methylphenidate-induced increase in rearing and sniffing in bisphenol-A (20 microg)-pretreated rats, the overall effects of methylphenidate on rearing, sniffing and grooming were similar in both vehicle- and bisphenol-A-pretreated rats. It is concluded that neonatal exposure of rats to bisphenol-A is an animal model with limited face validity for ADHD, because the motor hyperactivity and reduced habituation to a novel environment are not accompanied by altered responses to methylphenidate.

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Year:  2008        PMID: 18368283     DOI: 10.1007/s00702-008-0044-5

Source DB:  PubMed          Journal:  J Neural Transm (Vienna)        ISSN: 0300-9564            Impact factor:   3.575


  39 in total

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Journal:  Science       Date:  1999-01-15       Impact factor: 47.728

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Journal:  Pharmacol Biochem Behav       Date:  1995-10       Impact factor: 3.533

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Journal:  J Pharmacol Exp Ther       Date:  1983-11       Impact factor: 4.030

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  7 in total

1.  Neurobehavioral deficits, diseases, and associated costs of exposure to endocrine-disrupting chemicals in the European Union.

Authors:  Martine Bellanger; Barbara Demeneix; Philippe Grandjean; R Thomas Zoeller; Leonardo Trasande
Journal:  J Clin Endocrinol Metab       Date:  2015-03-05       Impact factor: 5.958

2.  Bisphenol-A exposure during adolescence leads to enduring alterations in cognition and dendritic spine density in adult male and female rats.

Authors:  Rachel E Bowman; Victoria Luine; Samantha Diaz Weinstein; Hameda Khandaker; Sarah DeWolf; Maya Frankfurt
Journal:  Horm Behav       Date:  2014-12-30       Impact factor: 3.587

3.  Topiramate via NMDA, AMPA/kainate, GABAA and Alpha2 receptors and by modulation of CREB/BDNF and Akt/GSK3 signaling pathway exerts neuroprotective effects against methylphenidate-induced neurotoxicity in rats.

Authors:  Majid Motaghinejad; Manijeh Motevalian; Sulail Fatima; Tabassom Beiranvand; Shiva Mozaffari
Journal:  J Neural Transm (Vienna)       Date:  2017-08-09       Impact factor: 3.575

4.  Combinations of physiologic estrogens with xenoestrogens alter calcium and kinase responses, prolactin release, and membrane estrogen receptor trafficking in rat pituitary cells.

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Journal:  Environ Health       Date:  2010-10-15       Impact factor: 5.984

5.  Transgenerational effects of prenatal bisphenol A on social recognition.

Authors:  Jennifer T Wolstenholme; Jessica A Goldsby; Emilie F Rissman
Journal:  Horm Behav       Date:  2013-10-05       Impact factor: 3.587

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

Authors:  Rachel E Bowman; Victoria Luine; Hameda Khandaker; Joseph J Villafane; Maya Frankfurt
Journal:  Synapse       Date:  2014-07-15       Impact factor: 2.562

7.  Diacylglycerol kinase β knockout mice exhibit attention-deficit behavior and an abnormal response on methylphenidate-induced hyperactivity.

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Journal:  PLoS One       Date:  2012-05-10       Impact factor: 3.240

  7 in total

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