Evidence map›Paper›PMID 39154755›Full record

ArticleBehavioural brain research2024

Late-term moderate prenatal alcohol exposure impairs tactile, but not spatial, discrimination in a T-maze continuous performance task in juvenile rats.

Caleb S Bailey, Ashley J Craig, Julia E Jagielo-Miller, Cassidy T Leibold, Peggy S Keller, Joshua S Beckmann, Mark A Prendergast

Abstract read
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Article in Behavioural brain research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Caleb S BaileyDepartment of Psychology, University of Kentucky, United States; Department of Neuroscience, University of Kentucky, United States. Electronic address: caleb.bailey@uky.edu.
Ashley J CraigDepartment of Neuroscience, University of Kentucky, United States.
Julia E Jagielo-MillerDepartment of Psychology, University of Kentucky, United States.
Cassidy T LeiboldDepartment of Psychology, University of Kentucky, United States.
Peggy S KellerDepartment of Psychology, University of Kentucky, United States.
Joshua S BeckmannDepartment of Psychology, University of Kentucky, United States.
Mark A PrendergastDepartment of Psychology, University of Kentucky, United States.

Funding

Training in Translational Research in Alzheimer's and Related Dementias (TRIAD)T32AG078110 · NIA · UNIVERSITY OF KENTUCKY · PI Michael Paul Murphy, LINDA J VAN ELDIK · 2022 to 2026
$2.3M
Interdisciplinary Training in Alcohol ResearchT32AA027488 · NIAAA · UNIVERSITY OF KENTUCKY · PI Mark T Fillmore, Mark A Prendergast · 2019 to 2026
$2.0M
NIAAA NIH HHS T32 AA027488NIA NIH HHS T32 AG078110
6 · The paper itself

Abstract

Existing maze apparatuses used in rodents often exclusively assess spatial discriminability as a means to evaluate learning impairments. Spatial learning in such paradigms is reportedly spared by moderate prenatal alcohol exposure in rats, suggesting that spatial reinforcement alone is insufficient to delineate executive dysfunction, which consistently manifests in humans prenatally-exposed to alcohol. To address this, we designed a single-session continuous performance task in the T-maze apparatus that requires rats to discriminate within and between simultaneously-presented spatial (left or right) and tactile (sandpaper or smooth) stimuli for food reinforcement across four sequential discrimination stages: simple discrimination, intradimensional reversal 1, extradimensional shift, and intradimensional reversal 2. This design incorporates elements of working memory, attention, and goal-seeking behavior which collectively contribute to the executive function construct. Here, we found that rats prenatally-exposed to alcohol performed worse in both the tactile intradimensional reversal and extradimensional shift; alternatively, rats prenatally-exposed to alcohol acquired the extradimensional shift faster when shifting from the tactile to spatial dimension. In line with previous work, moderate prenatal alcohol exposure spared specifically spatial discrimination in this paradigm. However, when tactile stimuli were mapped into the spatial dimension, rats prenatally-exposed to alcohol required more trials to discriminate between the dimensions. We demonstrate that tactile stimuli can be operantly employed in a continuous performance T-maze task to detect discriminatory learning impairments in rats exposed to moderate prenatal alcohol. The current paradigm may be useful for assessing features of executive dysfunction in rodent models of fetal alcohol spectrum disorders.

Indexed as

EthanolMaze LearningPrenatal Exposure Delayed EffectsAnimalsDiscrimination, PsychologicalFemaleFetal Alcohol Spectrum DisordersMaleMemory, Short-TermPregnancyRatsRats, Long-EvansSpace PerceptionTouchTouch PerceptionEthanolExecutive functionLearningPrenatal alcohol exposureT-mazeWorking memory

Identifiers

PMID39154755
PMCPMC11418090

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.