A Limited Access Mouse Model of Prenatal Alcohol Exposure that Produces Long-Lasting Deficits in Hippocampal-Dependent Learning and Memory

被引:95
作者
Brady, Megan L. [1 ]
Allan, Andrea M. [1 ]
Caldwell, Kevin K. [1 ]
机构
[1] Univ New Mexico, Sch Med, Dept Neurosci, Albuquerque, NM 87131 USA
关键词
Prenatal Ethanol Exposure; Learning; Memory; Hippocampus; Dentate Gyrus; DENTATE GYRUS; SPECTRUM DISORDERS; PATTERN SEPARATION; ETHANOL EXPOSURE; C57BL/6J MICE; SYNAPTIC PLASTICITY; DORSAL HIPPOCAMPUS; VOLUNTARY DRINKING; SPATIAL MEMORY; BEHAVIOR;
D O I
10.1111/j.1530-0277.2011.01644.x
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
100404 [儿少卫生与妇幼保健学];
摘要
Background: It has been estimated that approximately 12% of women consume alcohol at some time during their pregnancy, and as many as 5% of children born in the United States are impacted by prenatal alcohol exposure (PAE). The range of physical, behavioral, emotional, and social dysfunctions that are associated with PAE are collectively termed fetal alcohol spectrum disorder (FASD). Methods: Using a saccharin-sweetened ethanol solution, we developed a limited access model of PAE. C57BL/6J mice were provided access to a solution of either 10% (w/v) ethanol and 0.066% (w/v) saccharin or 0.066% (w/v) saccharin (control) for 4 h/d. After establishing consistent drinking, mice were mated and continued drinking during gestation. Following parturition, solutions were decreased to 0% in a stepwise fashion over a period of 6 days. Characterization of the model included measurements of maternal consumption patterns, blood ethanol levels, litter size, pup weight, maternal care, and the effects of PAE on fear-conditioned and spatial learning, and locomotor activity. Results: Mothers had mean daily ethanol intake of 7.17 +/- 0.17 g ethanol/kg body weight per day, with average blood ethanol concentrations of 68.5 +/- 9.2 mg/dl after 2 hours of drinking and 88.3 +/- 11.5 mg/dl after 4 hours of drinking. Food and water consumption, maternal weight gain, litter size, pup weight, pup retrieval times, and time on nest did not differ between the alcohol-exposed and control animals. Compared with control offspring, mice that were exposed to ethanol prenatally displayed no difference in spontaneous locomotor activity but demonstrated learning deficits in 3 hippocampal-dependent tasks: delay fear conditioning, trace fear conditioning, and the delay nonmatch to place radial-arm maze task. Conclusions: These results indicate that this model appropriately mimics the human condition of PAE and will be a useful tool in studying the learning deficits seen in FASD.
引用
收藏
页码:457 / 466
页数:10
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