Literature DB >> 12798963

Effects of perinatal exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin on spatial and visual reversal learning in rats.

John J Widholm1, Byung Woun Seo, Barbara J Strupp, Richard F Seegal, Susan L Schantz.   

Abstract

2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) is a ubiquitous environmental contaminant that has been shown to alter spatial and visual learning following developmental exposure. The current study examined the effects of gestational and lactational exposure to TCDD on spatial and visual discrimination/reversal learning (spatial and visual RL) in rats using two-lever operant testing chambers. Pregnant Sprague-Dawley rats (10 per dose) received either 0 or 0.1 microg/kg TCDD per orem in corn oil from gestational day (GD) 10 to GD 16. One male and one female from each litter were tested beginning at 100 days of age. For spatial RL, animals were reinforced for pressing the lever associated with the correct spatial location (either left or right). For visual RL, the animals were reinforced for pressing the lever associated with the correct visual stimulus (either the illuminated or nonilluminated cuelight). After reaching 85% correct for two consecutive days, the opposite spatial location or visual cue was reinforced. Five reversals were conducted for spatial RL, and two reversals for visual RL. For spatial RL, there were no differences between the TCDD-exposed and control rats in total number of errors committed. However, an in-depth analysis of errors in four different phases of the learning process revealed that TCDD-exposed rats made more errors early in learning when they were just beginning to learn the new reinforcement contingencies. The importance of this increase in errors during the initial stage of learning is unclear, given that there was no increase in overall errors to criterion. For visual RL, there was a reduction in errors on original learning (OL) for TCDD-exposed males, while TCDD-exposed females exhibited a reduction in errors on the second reversal. Subsequent response pattern analyses revealed that the facilitation in performance was due to a more rapid transition through the early phase of learning. Why males were improved on OL and females were not until the second reversal is unknown, but the different patterns could reflect differences in learning style in male and female rats. In keeping with previous research, the results of the current study underscore the fact that (1) alterations in cognitive function observed following early TCDD exposure are very subtle and (2) under some conditions, learning is actually facilitated, rather than impaired, in TCDD-exposed animals.

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Year:  2003        PMID: 12798963     DOI: 10.1016/s0892-0362(03)00014-x

Source DB:  PubMed          Journal:  Neurotoxicol Teratol        ISSN: 0892-0362            Impact factor:   3.763


  21 in total

1.  Testosterone impairs the acquisition of an operant delayed alternation task in male rats.

Authors:  Steven L Neese; Susan L Schantz
Journal:  Horm Behav       Date:  2011-10-25       Impact factor: 3.587

2.  Ahr and Cyp1a2 genotypes both affect susceptibility to motor deficits following gestational and lactational exposure to polychlorinated biphenyls.

Authors:  Breann T Colter; Helen Frances Garber; Sheila M Fleming; Jocelyn Phillips Fowler; Gregory D Harding; Molly Kromme Hooven; Amy Ashworth Howes; Smitha Krishnan Infante; Anna L Lang; Melinda Curran MacDougall; Melinda Stegman; Kelsey Rae Taylor; Christine Perdan Curran
Journal:  Neurotoxicology       Date:  2018-03       Impact factor: 4.294

3.  Prenatal dioxin exposure and neuropsychological functioning in the Seveso Second Generation Health Study.

Authors:  Jennifer Ames; Marcella Warner; Claudia Siracusa; Stefano Signorini; Paolo Brambilla; Paolo Mocarelli; Brenda Eskenazi
Journal:  Int J Hyg Environ Health       Date:  2019-01-09       Impact factor: 5.840

4.  Effects of multiple daily genistein treatments on delayed alternation and a differential reinforcement of low rates of responding task in middle-aged rats.

Authors:  Steven L Neese; Suren B Bandara; Daniel R Doerge; William G Helferich; Donna L Korol; Susan L Schantz
Journal:  Neurotoxicol Teratol       Date:  2011-09-14       Impact factor: 3.763

5.  Voluntary exercise impairs initial delayed spatial alternation performance in estradiol treated ovariectomized middle-aged rats.

Authors:  Steven L Neese; Donna L Korol; Susan L Schantz
Journal:  Horm Behav       Date:  2013-09-03       Impact factor: 3.587

6.  Cognitive flexibility deficits in male mice exposed to neonatal hyperoxia followed by concentrated ambient ultrafine particles.

Authors:  Keith Morris-Schaffer; Marissa Sobolewski; Kevin Welle; Katherine Conrad; Min Yee; Michael A O'Reilly; Deborah A Cory-Slechta
Journal:  Neurotoxicol Teratol       Date:  2018-10-11       Impact factor: 3.763

7.  Revealing Behavioral Learning Deficit Phenotypes Subsequent to In Utero Exposure to Benzo(a)pyrene.

Authors:  Monique M McCallister; Zhu Li; Tongwen Zhang; Aramandla Ramesh; Ryan S Clark; Mark Maguire; Blake Hutsell; M Christopher Newland; Darryl B Hood
Journal:  Toxicol Sci       Date:  2015-09-29       Impact factor: 4.849

Review 8.  The neural basis of reversal learning: An updated perspective.

Authors:  A Izquierdo; J L Brigman; A K Radke; P H Rudebeck; A Holmes
Journal:  Neuroscience       Date:  2016-03-12       Impact factor: 3.590

9.  Prenatal exposure to benzo(a)pyrene impairs later-life cortical neuronal function.

Authors:  Monique M McCallister; Mark Maguire; Aramandla Ramesh; Qiao Aimin; Sheng Liu; Habibeh Khoshbouei; Michael Aschner; Ford F Ebner; Darryl B Hood
Journal:  Neurotoxicology       Date:  2008-08-09       Impact factor: 4.294

10.  Behavioral changes in aging but not young mice after neonatal exposure to the polybrominated flame retardant decaBDE.

Authors:  Deborah C Rice; W Douglas Thompson; Elizabeth A Reeve; Kristen D Onos; Mina Assadollahzadeh; Vincent P Markowski
Journal:  Environ Health Perspect       Date:  2009-06-17       Impact factor: 9.031

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