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D-Cycloserine and Early Ethanol Exposure in Developing Rats

Bibliographic Data

ID13659013
AuthorsWalter Isaac (Georgia College & State University, corresponding author), W L Isaac (Georgia College & State University), William F McDaniel (Georgia College & State University), J D Corley (Georgia College & State University), S Emard (Georgia College & State University), Casey McDonald (0000-0002-9574-1711, Georgia College & State University), Lana K Young (Georgia College & State University), Christopher Ray (0000-0002-7925-5617, Georgia College & State University)
Year2009
Volume105
Issue2
Pages472-476
Publication date2009-10-01
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenuePsychological Reports (JOURNAL)
Journal identifiersISSN: 0033-2941 • E-ISSN: 1558-691X
PublisherSAGE Publishing (PUBLISHER • US)
DOI10.2466/pr0.105.2.472-476
PMID19928608
OpenAlexW2013007678
LanguageEN
References cited8

Pregnant rats were exposed to one of the following treatments: 20% aqueous sucrose (w/v; Control), 20% aqueous sucrose with 20 mg D-cycloserine (DCS), 20% aqueous sucrose with 5% ethanol (ETH), or 20% aqueous sucrose with both 20 mg DCS and 5% ethanol (DCS+ ETH). Treatments were delivered in 20 ml of drinking water provided daily, as pilot work had determined that this was the average daily water consumption for female rats. Treatments began on Day 10 or 11 of pregnancy and terminated on postnatal Day 10. As juveniles, offspring were tested for activity in an open field and motor coordination using a rotating rod. Ethanol and DCS+ Ethanol groups were the most active groups in the open field, and DCS and DCS+ Ethanol groups had fewer falls than the Control and Ethanol groups on the rod test. Results suggest that DCS might provide protection from ethanol's adverse effects on some developmental behaviors

Animal science · Aqueous solution · Biology · Ethanol · Offspring · Open field · Pregnancy · Sucrose · Biochemistry · Birth, Development, and Health · Chemistry · Internal Medicine · Medicine · Metabolism and Genetic Disorders · Prenatal Substance Exposure Effects

Citation velocityhistorical
Highly citedNo

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