» Articles » PMID: 39521144

The Effects of Moderate Prenatal Alcohol Exposure on Performance in Object and Spatial Discrimination Tasks by Adult Male Rats

Overview
Journal Behav Brain Res
Date 2024 Nov 9
PMID 39521144
Authors
Affiliations
Soon will be listed here.
Abstract

Exposure to alcohol during pregnancy produces Fetal Alcohol Spectrum Disorders, which in its most severe form is characterized by physical dysmorphology and neurobehavioral alterations. Moderate prenatal alcohol exposure (mPAE) is known to produce deficits in discrimination of spatial locations in adulthood. However, the impact of mPAE on higher-order sensory representations, such as discrimination of perceptually similar stimuli, is currently unknown. In the present study, we tested the hypothesis that mPAE would disrupt performance on hippocampal-sensitive tasks that require discrimination between perceptually similar objects or discrimination between spatial locations in a radial arm maze. Here we report that male mPAE rats exhibited intact performance on three types of object discrimination tasks: one in which rats discriminated between distinct toy objects, a second in which discrimination was made between distinct and similar LEGO objects, and a mnemonic similarity task in which rats discriminated between randomly presented LEGO objects that varied in similarity with a learned object. Although adult male mPAE rats performed similarly to control rats on all three object discrimination tasks, they showed deficits when tested in a radial arm maze spatial discrimination task. Specifically, male mPAE rats expressed a significantly higher number of working memory errors (returns to previously visited arms) and were more likely to use non-spatial strategies during training. Together, the findings of the present study support the conclusion that mPAE produces specific deficits in the online processing of spatial information and executing spatial navigation strategies, but spares the ability to discriminate between perceptually similar stimuli.

References
1.
Cacucci F, Yi M, Wills T, Chapman P, OKeefe J . Place cell firing correlates with memory deficits and amyloid plaque burden in Tg2576 Alzheimer mouse model. Proc Natl Acad Sci U S A. 2008; 105(22):7863-8. PMC: 2396558. DOI: 10.1073/pnas.0802908105. View

2.
Stevens S, Anstice N, Cooper A, Goodman L, ROGERs J, Wouldes T . Multiple Tools Are Needed for the Detection of Prenatal Alcohol Exposure: Findings From a Community Antenatal Setting. Alcohol Clin Exp Res. 2020; 44(4):1001-1011. DOI: 10.1111/acer.14309. View

3.
Rodriguez C, Magcalas C, Barto D, Fink B, Rice J, Bird C . Effects of sex and housing on social, spatial, and motor behavior in adult rats exposed to moderate levels of alcohol during prenatal development. Behav Brain Res. 2016; 313:233-243. PMC: 4987176. DOI: 10.1016/j.bbr.2016.07.018. View

4.
Davies S, Nelson D, Shrestha S, Savage D . Impact of two different rodent diets on maternal ethanol consumption, serum ethanol concentration and pregnancy outcome measures. Alcohol. 2023; 111:39-49. PMC: 10527634. DOI: 10.1016/j.alcohol.2023.05.002. View

5.
Terasaki L, Schwarz J . Effects of Moderate Prenatal Alcohol Exposure during Early Gestation in Rats on Inflammation across the Maternal-Fetal-Immune Interface and Later-Life Immune Function in the Offspring. J Neuroimmune Pharmacol. 2016; 11(4):680-692. PMC: 5525056. DOI: 10.1007/s11481-016-9691-8. View