A program of studies will investigate the neurophysiological basis of noradrenergic actions in neuronal circuits in the central nervous system.
The aim will be to establish a basis for the examination of the potential interactions between the noradrenergic system and three drugs of abuse: Amphetamine; cocaine and morphine. Function of the noradrenergic system will be examined in the cerebellum and cerebral cortex by employing microiontophoresis of drugs, stimulation of the locus corruleus, and physiological activation of somatosensory and visual afferent pathways. A new hypothesis will be explored which proposes that norepinephrine exerts a modulatory influence on synaptic efficacy in neuronal circuits. Specific studies on amphetamine will test for enhancement of noradrenergic synaptic function due to a combination of enhanced release of endogenous norepinephrine and direct agonist effects. Assays of noradrenergic NE action will also allow tests of the concept that cocaine in the central nervous system blocks norepinephrine release and reuptake processes. The improved criteria for identifying altered noradrenergic function will also be used to test whether morphine lowers tonic physiological noradrenergic activity by acting at terminals or within the locus coeruleus. Overall, the proposed research will contribute to a basic understanding of noradrenergic function, in parallel with tests to clarify the modes of action of drugs of abuse.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
5R01DA002338-07
Application #
3207268
Study Section
(SRC)
Project Start
1979-05-01
Project End
1986-11-30
Budget Start
1985-08-01
Budget End
1986-11-30
Support Year
7
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Type
Overall Medical
DUNS #
City
Dallas
State
TX
Country
United States
Zip Code
75390
Chang, J-Y; Chen, L; Luo, F et al. (2002) Neuronal responses in the frontal cortico-basal ganglia system during delayed matching-to-sample task: ensemble recording in freely moving rats. Exp Brain Res 142:67-80
Chang, J Y; Janak, P H; Woodward, D J (2000) Neuronal and behavioral correlations in the medial prefrontal cortex and nucleus accumbens during cocaine self-administration by rats. Neuroscience 99:433-43
Woodward, D J; Chang, J Y; Janak, P et al. (2000) Activity patterns in mesolimbic regions in rats during operant tasks for reward. Prog Brain Res 126:303-22
Kampman, K M; Volpicelli, J R; Alterman, A I et al. (2000) Amantadine in the treatment of cocaine-dependent patients with severe withdrawal symptoms. Am J Psychiatry 157:2052-4
Woodward, D J; Chang, J Y; Janak, P et al. (1999) Mesolimbic neuronal activity across behavioral states. Ann N Y Acad Sci 877:91-112
Chang, J Y; Janak, P H; Woodward, D J (1998) Comparison of mesocorticolimbic neuronal responses during cocaine and heroin self-administration in freely moving rats. J Neurosci 18:3098-115
Chang, J Y; Sawyer, S F; Paris, J M et al. (1997) Single neuronal responses in medial prefrontal cortex during cocaine self-administration in freely moving rats. Synapse 26:22-35
Chang, J Y; Zhang, L; Janak, P H et al. (1997) Neuronal responses in prefrontal cortex and nucleus accumbens during heroin self-administration in freely moving rats. Brain Res 754:12-20
Chang, J Y; Paris, J M; Sawyer, S F et al. (1996) Neuronal spike activity in rat nucleus accumbens during cocaine self-administration under different fixed-ratio schedules. Neuroscience 74:483-97
Lee, R S; Smith, S S; Chapin, J K et al. (1995) Effects of systemic and local ethanol on responses of rat cerebellar Purkinje neurons to iontophoretically applied gamma-aminobutyric acid. Brain Res 687:1-11

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