Gestational-lactational exposure to Aroclor 1254 impairs radial-arm maze performance in male rats

被引:78
|
作者
Roegge, CS
Seo, BW
Crofton, KM
Schantz, SL
机构
[1] Univ Illinois, Dept Vet Biosci, Coll Vet Med, Urbana, IL 61802 USA
[2] Univ Illinois, Program Neurosci, Urbana, IL 61801 USA
[3] GD Searle & Co, Global Healthcare Resources, Skokie, IL 60077 USA
[4] US EPA, Natl Hlth & Environm Effects Res Lab, Div Neurotoxicol, Res Triangle Pk, NC 27711 USA
关键词
PCB; Aroclor; 1254; gestational-lactational exposure; spatial learning and memory; radial-arm maze; rats; drug challenges;
D O I
10.1093/toxsci/57.1.121
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Developmental exposure to polychlorinated biphenyls (PCBs) has been associated with cognitive deficits in children. The current study assessed effects of gestational and lactational exposure to a commercial PCB mixture, Aroclor 1254 (A1254), on spatial learning and memory in rats, using the radial-arm maze (RAM). Pregnant Long-Evans females (10/dose group) were exposed to 0 or 6-mg/kg/day A1254 (po in corn oil) from gestation day (GD)6 to weaning at postnatal day (PND) 21, After they reached adulthood, 1 male and 1 female from each litter were tested on a working/reference memory task using a 12-arm RAM. Eight of the 12 arms were baited, with the pattern of baited arms remaining the same on every trial for each rat. Compared to control males, the A1254-exposed males made significantly more working memory errors (2.15 +/- 0.13 and 3.20 +/- 0.18 errors +/- SEM for control and A1254 males, respectively) and reference memory errors (3.17 +/- 0.10 and 4.13 +/- 0.14 errors +/- SEM for control and A1254 males, respectively) on the RAM. In contrast, A1254-exposed females were not impaired relative to control females on the RAM. Drug challenges with dizocilpine (MK-801) and scopolamine did not differentially affect working or reference memory of control and exposed rats. These data suggest that perinatal exposure to A1254 may cause sex-specific deficits in spatial learning and memory, and that NMDA-mediated and muscarinic neurotransmission, as assessed with the drug challenges, were not markedly impaired in the A1254-exposed animals.
引用
收藏
页码:121 / 130
页数:10
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