Toxicological Sciences 60, 315-326 (2001)
Copyright © 2001 by the Society of Toxicology
NEUROTOXICOLOGY |
Neurotoxicological Outcomes of Perinatal Heptachlor Exposure in the Rat
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* Neurotoxicology Division, National Health and Environmental Effects Research Laboratory, Office of Research and Development, U.S. EPA, Research Triangle Park, North Carolina;
Reproductive Toxicology Group, National Toxicology Program, NIEHS, Research Triangle Park, North Carolina
The developing nervous system has been identified as a potential target of pesticide exposure. Heptachlor is a cyclodiene pesticide that was widely used for many years, and for which inadvertent exposure to children and fetuses took place in the early 1980s; yet little is known regarding the developmental neurotoxicity of it and other cyclodienes. The aim of this study was to determine whether perinatal heptachlor exposure results in persistent alterations in nervous system function. Pregnant Sprague-Dawley dams were dosed from gestational day (GD) 12 to postnatal day (PND) 7, whereupon the rat pups were dosed directly until PND 21 (group A) or PND 42 (group B). Dose levels were 0, 0.03, 0.3, or 3 mg/kg/day, po. There were no dose-related effects on maternal weight, litter size, or pup growth. GABAA receptor binding (using [35S] tert-butylbicyclophosphorothionate; TBPS) and GABA-stimulated Cl– flux were evaluated in control and high-dose brain tissues taken on PND 7, 21, and 43. The Bmax values for [35S]-TBPS binding in brainstem, but not cortex, were decreased in female rats across all ages tested. There were no such changes in male rats, nor were KD values altered in either tissue or gender. GABA-stimulated Cl– flux was decreased in female cortex synaptoneurosomes only on PND 21. The ontogeny of the righting response (PND 2–5) was delayed in the high-dose females. All subsequent testing took place a week to months after dosing ceased. The functional observational battery (FOB) showed treatment-related, but not necessarily dose-related, changes in different aspects of the rat's reactivity and activity levels. Group-A rats also showed altered within-session habituation of motor activity. There were no heptachlor-related differences in motor activity following challenge with a range of chlordiazepoxide doses. Cognitive assessments were conducted in both groups of rats. There were no statistically significant differences among treatment groups in a one-trial passive avoidance test, although there was a trend toward less learning. In group B, rats (both sexes), heptachlor altered spatial learning in the Morris water maze during two weeks of daily training (2 trials/day). On probe trials, heptachlor-treated rats did not show significant preference for the correct quadrant (all dose groups in males, high dose in females). These rats did not show alterations on subsequent working-memory training (where the platform position was relearned each day). Thus, perinatal exposure to heptachlor produced neurochemical and persistent neurobehavioral changes, including alterations in spatial learning and memory.
Key Words: heptachlor; developmental neurotoxicity; Morris water maze; pesticide exposure.
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