The primary long-term goal of this project is to understand the neural mechanisms that contribute to the self-administration of opiate and stimulant drugs of abuse. Behavioral pharmacological methodologies will be applied to address three specific aims each of which builds upon and/or extends work conducted during the first fourteen years of this project. These are: 1) To dissociate the underlying motivational processes that serve to initiate drug-seeking behavior, from the reinforcing processes that are activated as a consequence of drug self-administration; 2) To continue and extend investigations of the mechanisms involved in the """"""""relapse"""""""" of drug-abuse behavior as modeled in an operant runway test of response-reinstatement; and 3) To continue investigation of the nature and neurobiology of the putative anxiogenic/aversive properties of self-administered cocaine. The primary self-administration methodology employed in this work is a unique operant runway test of IV drug reinforcement. Animals are trained to traverse a straight arm runway once each day for a reward consisting of IV drug reinforcement (i.e., cocaine, heroin, speedball, nomefensine, cocaethylene) delivered upon the Ss' entry into the goal box. In this context, the speed with which the undrugged animal traverses the runway to return to a place where it had previously received the drug reinforcer, provides a valid and highly reliable index of the Ss' motivation to obtain the reinforcer. In addition, because the animals are tested on a single trial per day, the resulting operant data are devoid of nonspecific effects produced by the drug reinforcers themselves. Since motivated states (including those activate drug-seeking behavior) are defined, in part, by the presence of internal activation or arousal, the project has begun the use of small implanted radio-telemetric devices that provide physiological data (heart rate, respiration, ECG, core temperature...) about the internal state of the animal during behavioral testing. The combination of these behavioral and physiological measures will permit the initiation of studies intended to investigate the complex relationship between central and sympathetic nervous systems in the production of motivated behavior. Experiments are planned on the IV and IC self-administration of reinforcing drugs in the runway, on the underlying mechanisms that produce the """"""""activation"""""""" of drug-seeking behavior upon presentation of drug-predictive environmental stimuli.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
5R01DA005041-19
Application #
7231390
Study Section
Integrative, Functional and Cognitive Neuroscience 8 (IFCN)
Program Officer
Lynch, Minda
Project Start
1988-03-01
Project End
2008-04-30
Budget Start
2007-05-01
Budget End
2008-04-30
Support Year
19
Fiscal Year
2007
Total Cost
$209,785
Indirect Cost
Name
University of California Santa Barbara
Department
Psychology
Type
Schools of Arts and Sciences
DUNS #
094878394
City
Santa Barbara
State
CA
Country
United States
Zip Code
93106
Ettenberg, Aaron; Fomenko, Vira; Kaganovsky, Konstantin et al. (2015) On the positive and negative affective responses to cocaine and their relation to drug self-administration in rats. Psychopharmacology (Berl) 232:2363-75
Wenzel, Jennifer M; Cotten, Samuel W; Dominguez, Hiram M et al. (2014) Noradrenergic ?-receptor antagonism within the central nucleus of the amygdala or bed nucleus of the stria terminalis attenuates the negative/anxiogenic effects of cocaine. J Neurosci 34:3467-74
Su, Zu-In; Santoostaroam, Ashley; Wenzel, Jennifer et al. (2013) On the persistence of cocaine-induced place preferences and aversions in rats. Psychopharmacology (Berl) 229:115-23
Kerstetter, Kerry A; Su, Zu-In; Ettenberg, Aaron et al. (2013) Sex and estrous cycle differences in cocaine-induced approach-avoidance conflict. Addict Biol 18:222-9
Wenzel, Jennifer M; Su, Zu-In; Shelton, Kerisa et al. (2013) The dopamine antagonist cis-flupenthixol blocks the expression of the conditioned positive but not the negative effects of cocaine in rats. Pharmacol Biochem Behav 114-115:90-6
Su, Zu-In; Kichaev, Gleb; Wenzel, Jennifer et al. (2012) Weakening of negative relative to positive associations with cocaine-paired cues contributes to cue-induced responding after drug removal. Pharmacol Biochem Behav 100:458-63
Ettenberg, Aaron; Ofer, Oren A; Mueller, Carl L et al. (2011) Inactivation of the dorsal raphe nucleus reduces the anxiogenic response of rats running an alley for intravenous cocaine. Pharmacol Biochem Behav 97:632-9
Wenzel, Jennifer M; Waldroup, Stephanie A; Haber, Zachary M et al. (2011) Effects of lidocaine-induced inactivation of the bed nucleus of the stria terminalis, the central or the basolateral nucleus of the amygdala on the opponent-process actions of self-administered cocaine in rats. Psychopharmacology (Berl) 217:221-30
Su, Zu-In; Wenzel, Jennifer; Baird, Rebeccah et al. (2011) Comparison of self-administration behavior and responsiveness to drug-paired cues in rats running an alley for intravenous heroin and cocaine. Psychopharmacology (Berl) 214:769-78
Moscarello, J M; Ben-Shahar, O; Ettenberg, A (2010) External incentives and internal states guide goal-directed behavior via the differential recruitment of the nucleus accumbens and the medial prefrontal cortex. Neuroscience 170:468-77

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