The work outlined in this proposal will examine further the neurobehavioral consequences of early cocaine exposure. Two of the most robust behavioral alterations observed during the previous project period in offspring of sprague-Dawley dams exposed subcutaneously to cocaine from gestational days 8-20, relative to offspring of pair-fed and untreated control dams, were; (a) their unusual behavioral response to stressors and (b) the cognitive deficits they exhibit in complex or presumably stressful testing situations. Apparent attenuations in dopamine (DA) activity were observed on some response measures, but not others, leading to the hypothesis that the underlying DA deficiency may be functionally countered by neural compensatory processes under basal conditions, but may be """"""""unmasked"""""""" under challenging or stressful test circumstances. The work outlined in this proposal will examine the alterations in cocaine-exposed offspring under these two types of """"""""challenges,"""""""" with an emphasis on possible alterations in DA function as contributing factors to these long-term behavioral consequences of gestational cocaine exposure. Experimental Series 1 will examine the behavioral responses to acute stressors in adult offspring prenatally exposed to cocaine as well as their behavioral, neurochemical and hormonal response to acute and repeated stressors. The intent of these studies is to evaluate in what ways the behavioral responsivity to stressors has been altered by prenatal cocaine exposure, and to determine whether similar alterations in stress responsivity are seen using hormonal and neurochemical response measures, with a particular emphasis in the latter on assessment of alterations in responsiveness of the DA systems to stressors. Experimental Series 2 will focus further on behavioral assessments in these offspring. The first studies in this series will examine whether adult cocaine-exposed offspring exhibit not only deficits in reversal performance, but alterations in other behaviors that have been associated with disruption of DA terminal regions. The second part of this series will examine in more detail the cognitive alterations in these offspring by assessing what behavioral features and processes lead to their alterations in cognitive performance. At this early stage in the investigation of the developmental toxicology of cocaine, such animal research is critical to confirm and extend potentially confounded clinical findings, to anticipate other potential consequences of early cocaine exposure, as well as to offer insights into the mechanisms influencing the developmental outcome of the large number of children that have been exposed prenatally to this drug of abuse.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
2R01DA004478-08A1
Application #
2117215
Study Section
Drug Abuse Biomedical Research Review Committee (DABR)
Project Start
1987-09-01
Project End
2000-02-29
Budget Start
1995-03-15
Budget End
1996-02-29
Support Year
8
Fiscal Year
1995
Total Cost
Indirect Cost
Name
State University of NY, Binghamton
Department
Psychology
Type
Schools of Arts and Sciences
DUNS #
090189965
City
Binghamton
State
NY
Country
United States
Zip Code
13902
Hecht, G S; Spear, N E; Spear, L P (1999) Changes in progressive ratio responding for intravenous cocaine throughout the reproductive process in female rats. Dev Psychobiol 35:136-45
Campbell, J; Spear, L P (1999) Effects of early handling on amphetamine-induced locomotor activation and conditioned place preference in the adult rat. Psychopharmacology (Berl) 143:183-9
Campbell, J O; Fogarty, J A; Spear, L P (1999) Inhibition of nitric oxide synthesis with L-NAME suppresses isolation-induced ultrasounds in rat pups. Pharmacol Biochem Behav 63:45-53
Katovic, N M; Gresack, J E; Spear, L P (1999) Schedule-induced polydipsia: gender-specific effects and consequences of prenatal cocaine and postnatal handling. Pharmacol Biochem Behav 64:695-704
Hecht, G S; Spear, N E; Spear, L P (1998) Alterations in the reinforcing efficacy of cocaine in adult rats following prenatal exposure to cocaine. Behav Neurosci 112:410-8
Snyder, K J; Katovic, N M; Spear, L P (1998) Longevity of the expression of behavioral sensitization to cocaine in preweanling rats. Pharmacol Biochem Behav 60:909-14
Spear, L P; Campbell, J; Snyder, K et al. (1998) Animal behavior models. Increased sensitivity to stressors and other environmental experiences after prenatal cocaine exposure. Ann N Y Acad Sci 846:76-88
Wood, R D; Tirelli, E; Snyder, K J et al. (1998) Evidence for behavioral sensitization to cocaine in preweanling rat pups. Psychopharmacology (Berl) 138:114-23
Wood, R D; Spear, L P (1998) Prenatal cocaine alters social competition of infant, adolescent, and adult rats. Behav Neurosci 112:419-31
Laviola, G; Wood, R D; Kuhn, C et al. (1995) Cocaine sensitization in periadolescent and adult rats. J Pharmacol Exp Ther 275:345-57

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