Prenatal exposure to alcohol can result in a variety of morphological and behavioral abnormalities in humans. However, there are wide variations in outcome given similar alcohol exposure histories and it has been proposed that differential tolerance to ethanol might be one reason for this variation. Therefore, one aim of the current proposal is to determine if the degree of tolerance to ethanol influences the severity of alcohol's effects. Rat pups from two selectively bred lines the P and NP lines, will be studied for their susceptibility to the effects of alcohol exposure. While these lines were bred for extremes in alcohol preference they also differ in their development of tolerance to ethanol. These two lines and Sprague-Dawley rats will be exposed to ethanol during a period of rapid brain growth, while ensuring adequate nutrition. Rats exposed to ethanol using this procedure show a variety of central nervous system anomalies and a limited number of studies suggest that behavior may be particularly affected by exposure during this period. Data also indicate that many of the behavioral problems seen in children exposed to alcohol in utero are more severe if the mother drinks throughout her pregnancy than if she stops drinking prior to the third trimester, when the brain growth spurt occurs. Thus in addition to looking at the role differential tolerance may play in alcohol's teratogenic effects, we will further characterize behavioral dysfunctions associated with ethanol exposure during this period and determine the permanence of such effects.

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Research Project (R01)
Project #
5R01AA006902-07
Application #
3110329
Study Section
Biochemistry, Physiology and Medicine Subcommittee (ALCB)
Project Start
1988-09-30
Project End
1994-02-28
Budget Start
1991-03-01
Budget End
1992-02-29
Support Year
7
Fiscal Year
1991
Total Cost
Indirect Cost
Name
San Diego State University
Department
Type
Schools of Arts and Sciences
DUNS #
073371346
City
San Diego
State
CA
Country
United States
Zip Code
92182
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Idrus, Nirelia M; Thomas, Jennifer D (2011) Fetal alcohol spectrum disorders: experimental treatments and strategies for intervention. Alcohol Res Health 34:76-85
Idrus, Nirelia M; McGough, Nancy N H; Spinetta, Michael J et al. (2011) The effects of a single memantine treatment on behavioral alterations associated with binge alcohol exposure in neonatal rats. Neurotoxicol Teratol 33:444-50
Idrus, Nirelia M; McGough, Nancy N H; Riley, Edward P et al. (2011) Administration of memantine during ethanol withdrawal in neonatal rats: effects on long-term ethanol-induced motor incoordination and cerebellar Purkinje cell loss. Alcohol Clin Exp Res 35:355-64
McGough, Nancy N H; Thomas, Jennifer D; Dominguez, Hector D et al. (2009) Insulin-like growth factor-I mitigates motor coordination deficits associated with neonatal alcohol exposure in rats. Neurotoxicol Teratol 31:40-8
Bell, Matthew C; Riley, Edward P (2006) Memory and perseveration on a win-stay, lose-shift task in rats exposed neonatally to alcohol. J Stud Alcohol 67:851-60
Sakata-Haga, Hiromi; Dominguez, Hector D; Sei, Hiroyoshi et al. (2006) Alterations in circadian rhythm phase shifting ability in rats following ethanol exposure during the third trimester brain growth spurt. Alcohol Clin Exp Res 30:899-907
Thomas, J D; Garcia, G G; Dominguez, H D et al. (2004) Administration of eliprodil during ethanol withdrawal in the neonatal rat attenuates ethanol-induced learning deficits. Psychopharmacology (Berl) 175:189-95
Slawecki, Craig J; Thomas, Jennifer D; Riley, Edward P et al. (2004) Neurophysiologic consequences of neonatal ethanol exposure in the rat. Alcohol 34:187-96
Thomas, J D; Leany, B D; Riley, E P (2003) Differential vulnerability to motor deficits in second replicate HAS and LAS rats following neonatal alcohol exposure. Pharmacol Biochem Behav 75:17-24

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