Literature DB >> 17466489

Prenatal methylmercury exposure increases responding under clocked and unclocked fixed interval schedules of reinforcement.

Miranda N Reed1, M Christopher Newland.   

Abstract

Recent experiments have suggested that developmental methylmercury exposure produces perseverative behavior in adulthood. In the present experiment, interactions between developmental low-level methylmercury (MeHg) and nutritionally relevant dietary selenium (Se) on operant behavior and its persistence were examined in aged animals. Female rats were exposed, in utero, to 0, 0.5, or 5 ppm mercury as MeHg via drinking water, approximating mercury exposures of 0, 40, and 400 microg/kg/day. They also received both pre- and chronic post-natal exposure to a diet that was marginal (0.06 ppm) or rich (0.6 ppm) in Se, a nutrient believed to protect against MeHg's toxicity. This created a 2 (chronic Se)x3 (gestational MeHg) full factorial design, with 6-8 female rats per cell. At eleven months of age, a multiple schedule consisting of alternating fixed interval (FI) and clocked FI (CFI) components was arranged. The CFI component was divided into 5, 24-second bins, each associated with a different auditory stimulus, providing a "clock." Low and high response rates were evaluated using the initial 40% (bins 1 and 2) and last 20% (bin 5) of the FI and CFI components, respectively. Rats exposed to 5 ppm Hg made more responses than the other two groups during the last 20% of the intervals, regardless of selenium exposure or presence of the clock stimuli. They did not differ from the other groups during the initial 40% of the FI and CFI components. Following reinforcement omission for half of the intervals at 21 months of age, the 5 ppm Hg group continued to respond at higher rates than the other groups in both components.

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Year:  2007        PMID: 17466489     DOI: 10.1016/j.ntt.2007.03.002

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


  7 in total

1.  Sex-dependent and non-monotonic enhancement and unmasking of methylmercury neurotoxicity by prenatal stress.

Authors:  Hiromi I Weston; Marissa E Sobolewski; Joshua L Allen; Doug Weston; Katherine Conrad; Sean Pelkowski; Gene E Watson; Grazyna Zareba; Deborah A Cory-Slechta
Journal:  Neurotoxicology       Date:  2014-02-03       Impact factor: 4.294

Review 2.  A hypothesis about how early developmental methylmercury exposure disrupts behavior in adulthood.

Authors:  M Christopher Newland; Miranda N Reed; Erin Rasmussen
Journal:  Behav Processes       Date:  2015-03-17       Impact factor: 1.777

Review 3.  Behavioral effects of developmental methylmercury drinking water exposure in rodents.

Authors:  Emily B Bisen-Hersh; Marcelo Farina; Fernando Barbosa; Joao B T Rocha; Michael Aschner
Journal:  J Trace Elem Med Biol       Date:  2013-10-07       Impact factor: 3.849

4.  Developmental exposure to PCBs and/or MeHg: effects on a differential reinforcement of low rates (DRL) operant task before and after amphetamine drug challenge.

Authors:  Helen J K Sable; Paul A Eubig; Brian E Powers; Victor C Wang; Susan L Schantz
Journal:  Neurotoxicol Teratol       Date:  2009-01-21       Impact factor: 3.763

5.  Response inhibition is impaired by developmental methylmercury exposure: acquisition of low-rate lever-pressing.

Authors:  M Christopher Newland; Daniel J Hoffman; John C Heath; Wendy D Donlin
Journal:  Behav Brain Res       Date:  2013-05-27       Impact factor: 3.332

Review 6.  Prenatal influences on temperament development: The role of environmental epigenetics.

Authors:  Maria A Gartstein; Michael K Skinner
Journal:  Dev Psychopathol       Date:  2017-12-12

7.  Limited developmental neurotoxicity from neonatal inhalation exposure to diesel exhaust particles in C57BL/6 mice.

Authors:  Keith Morris-Schaffer; Alyssa K Merrill; Candace Wong; Katrina Jew; Marissa Sobolewski; Deborah A Cory-Slechta
Journal:  Part Fibre Toxicol       Date:  2019-01-07       Impact factor: 9.400

  7 in total

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