The Journal of Neuroscience, December 1, 2000, 20(23):8902-8908
Prenatal Cocaine Exposure Increases Sensitivity to the
Attentional Effects of the Dopamine D1 Agonist SKF81297
Lorna E.
Bayer1,
Alison
Brown1,
Charles F.
Mactutus3,
Rose M.
Booze4, and
Barbara J.
Strupp1, 2
1 Department of Psychology and 2 Division
of Nutritional Sciences, Cornell University, Ithaca, New York 14853, and 3 Division of Pharmacology and Experimental
Therapeutics, College of Pharmacy, Tobacco and Health Research
Institute, Graduate Center for Toxicology, and 4 Department
of Anatomy and Neurobiology, College of Medicine, University of
Kentucky, Lexington, Kentucky 40546
Sensitivity to the attentional effects of SKF81297, a selective
full agonist at dopamine D1 receptors, was assessed in
adult rats exposed to cocaine prenatally (via intravenous injections) and controls. The task assessed the ability of the subjects to monitor
an unpredictable light cue of either 300 or 700 msec duration and to
maintain performance when presented with olfactory distractors. SKF81297 decreased nose pokes before cue presentation and increased latencies and response biases (the tendency to respond to the same port
used on the previous trial), suggesting an effect of SKF81297 on the
dopamine (DA) systems responsible for response initiation and
selection. The cocaine-exposed (COC) and control animals did not differ
in sensitivity to the effects of SKF81297 on these measures. In
contrast, the COC animals were significantly more sensitive than were
controls to the impairing effect of SKF81297 on omission errors, a
measure of sustained attention. This pattern of results provides
evidence that prenatal cocaine exposure produces lasting changes in the
DA system(s) subserving sustained attention but does not alter the DA
system(s) underlying response selection and initiation. These findings
also provide support for the role of D1 receptor activation
in attentional functioning.
Key words:
prenatal cocaine; intravenous injection; catecholamine; dopamine; attention; response initiation; response selection
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