Damage to the orbitofrontal cortex (OFC) may contribute to persistent craving and compulsive drug seeking in former drug users. Consistent with this, lOFC lesions induced prior to self-administration training potentiate context-induced cocaine seeking in a rat model of drug relapse. The guiding hypothesis of this proposal is that prolonged loss of output from the lOFC enhances context-induced motivation for cocaine by eliciting compensatory neuroadaptations in other elements of the brain circuitry of drug relapse. Overall, this proposal will utilize the contextual extinction-reinstatement model of drug relapse in which rats are trained to self-administer cocaine in a distinct environmental context, followed by extinction training in a different context. Context-induced motivation for cocaine is then assessed in the cocaine-paired context in the absence of cocaine reinforcement.
Specific Aim 1 will test the hypothesis that pre-training lOFC lesions prompt enhanced context-induced motivation for cocaine and associated compensatory neuroadaptations in immediate-early gene (lEG) expression in elements of the mesocorticolimbic relapse circuitry. To this end, we will administer lesions of the lOFC prior to cocaine self-administration training and then use in situ hybridization histochemistry to assess mRNA expression of the activity-dependent lEG zinc finger 268 (zif268) and brain-derived neurotrophic factor (BDNF), following reinstatement testing in the cocaine-paired context.
Specific Aim 2 will test the hypothesis that reversing lOFC lesion-induced increases in zif268 and BDNF expression in critical brain regions will abolish lOFC lesion-induced enhancement in context-induced motivation for cocaine. To assess whether lOFC lesion-induced increases in lEG expression are necessary for enhanced context-induced reinstatement, immediately before reinstatement testing, rats with pre-training lOFC lesions will receive zif268 or BDNF antisense oligodeoxynucleotide infusions into brain regions that exhibit the most robust elevation in zif268 or BDNF expression in the lOFC lesion vs. sham groups. Public Health Relevance: Cocaine addiction is a prominent health and social issue in the United States, with about 1.6 million individual classified as cocaine dependent (2007 NSDUH, NIDA). OFC damage in cocaine addicts has been theorized to promote addictive behavior and the proposed project utilizes a rodent model of drug relapse to explore the cellular and functional neuroanatomical mechanisms of this phenomenon. Understanding the neural mechanisms underlying of OFC lesion-induced loss of control in drug seeking may offer critical insight for addiction treatment development.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
5F31DA028051-02
Application #
8271252
Study Section
Special Emphasis Panel (ZRG1-F01-W (20))
Program Officer
Babecki, Beth
Project Start
2010-07-01
Project End
2011-12-18
Budget Start
2011-07-01
Budget End
2011-12-18
Support Year
2
Fiscal Year
2011
Total Cost
$16,673
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Psychology
Type
Schools of Arts and Sciences
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Lasseter, Heather C; Xie, Xiaohu; Arguello, Amy A et al. (2014) Contribution of a mesocorticolimbic subcircuit to drug context-induced reinstatement of cocaine-seeking behavior in rats. Neuropsychopharmacology 39:660-9
Arguello, Amy A; Hodges, Matthew A; Wells, Audrey M et al. (2014) Involvement of amygdalar protein kinase A, but not calcium/calmodulin-dependent protein kinase II, in the reconsolidation of cocaine-related contextual memories in rats. Psychopharmacology (Berl) 231:55-65
Wells, Audrey M; Arguello, Amy A; Xie, Xiaohu et al. (2013) Extracellular signal-regulated kinase in the basolateral amygdala, but not the nucleus accumbens core, is critical for context-response-cocaine memory reconsolidation in rats. Neuropsychopharmacology 38:753-62
Xie, Xiaohu; Arguello, Amy A; Wells, Audrey M et al. (2013) Role of a hippocampal SRC-family kinase-mediated glutamatergic mechanism in drug context-induced cocaine seeking. Neuropsychopharmacology 38:2657-65
Xie, Xiaohu; Lasseter, Heather C; Ramirez, Donna R et al. (2012) Subregion-specific role of glutamate receptors in the nucleus accumbens on drug context-induced reinstatement of cocaine-seeking behavior in rats. Addict Biol 17:287-99
Lasseter, Heather C; Wells, Audrey M; Xie, Xiaohu et al. (2011) Interaction of the basolateral amygdala and orbitofrontal cortex is critical for drug context-induced reinstatement of cocaine-seeking behavior in rats. Neuropsychopharmacology 36:711-20
Lasseter, H C; Xie, X; Ramirez, D R et al. (2010) Sub-region specific contribution of the ventral hippocampus to drug context-induced reinstatement of cocaine-seeking behavior in rats. Neuroscience 171:830-9
Lasseter, Heather C; Xie, Xiaohu; Ramirez, Donna R et al. (2010) Prefrontal cortical regulation of drug seeking in animal models of drug relapse. Curr Top Behav Neurosci 3:101-17
Lasseter, Heather C; Ramirez, Donna R; Xie, Xiaohu et al. (2009) Involvement of the lateral orbitofrontal cortex in drug context-induced reinstatement of cocaine-seeking behavior in rats. Eur J Neurosci 30:1370-81