In this application for an NIDA-NIH Independent Scientist Award (ISA) a program of research is proposed to elucidate brain opioid mechanisms that facilitate reward during chronic food restriction. A multidisciplinary approach to this problem is planned which exploits recently developed molecular biological methodologies. Previous research indicates that metabolic need states activate a brain opioid mechanism that sensitizes animals to rewarding effects of electrical brain stimulation. Evidence for the involvement of mu and kappa opioid receptors along with dynorphin A peptides has been obtained. In Studies I and II the changes in plasma corticosterone and insulin associated with metabolic need will be investigated as possible triggers of reward sensitization. Studies III and IV follow observations that food restriction produces brain regional changes in dynorphin peptide levels and mu and kappa receptor binding. Solution hybridization and in situ hybridization histochemistry will be used to elucidate these changes by seeking corresponding changes in receptor and prodynorphin gene transcription. In Study V [35S]GTP-gammaS autoradiography will be used to investigate the neuroanatomical distribution of changes in G-protein activation. Since food restriction appears to be accompanied by a tonic increase in opioid peptide release, c-fos immunohistochemistry will be used in Study VI to identify brain regions that display 'rebound' activation in response to naltrexone. Study VII will utilize microinjections of antagonists, antisense oligodeoxynucleotides and antibodies to opioid peptides to identify the brain region(s) and intrinsic peptide-receptor type combinations that mediate the sensitization of reward. In addition to supporting a research program, the ISA will provide the PI with opportunities for training in molecular biological approaches that increase the power of behavioral neuroscientific investigation. This training, which will occur by way of collaboration with several colleagues, will enhance the ability of the PI to bring modern neuroscientific methods to bear on the solution of basic behavioral problems relating to motivation and reward. During the period of ISA support, the Pl, who is Associate Director of the Postdoctoral Training Program, will serve as mentor to trainees as well as residents and fellows in the Division of Alcoholism and Substance Abuse. The long-term support and commitment to the PI's scientific development engendered by the ISA will ensure the stability and productivity of the laboratory, thereby creating an improved setting for research training.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Scientist Development Award - Research (K02)
Project #
5K02DA000292-03
Application #
2897616
Study Section
Human Development Research Subcommittee (NIDA)
Program Officer
Volman, Susan
Project Start
1997-05-01
Project End
2002-04-30
Budget Start
1999-05-01
Budget End
2000-04-30
Support Year
3
Fiscal Year
1999
Total Cost
Indirect Cost
Name
New York University
Department
Psychiatry
Type
Schools of Medicine
DUNS #
City
New York
State
NY
Country
United States
Zip Code
10016
Cabeza de Vaca, Soledad; Kannan, Pavitra; Pan, Yan et al. (2007) The adenosine A2A receptor agonist, CGS-21680, blocks excessive rearing, acquisition of wheel running, and increases nucleus accumbens CREB phosphorylation in chronically food-restricted rats. Brain Res 1142:100-9
Lin, Yan; de Vaca, Soledad Cabeza; Carr, Kenneth D et al. (2007) Role of alpha(1)-adrenoceptors of the locus coeruleus in self-stimulation of the medial forebrain bundle. Neuropsychopharmacology 32:835-41
Carr, Kenneth D (2007) Chronic food restriction: enhancing effects on drug reward and striatal cell signaling. Physiol Behav 91:459-72
Pan, Yan; Siregar, Ermanda; Carr, Kenneth D (2006) Striatal cell signaling in chronically food-restricted rats under basal conditions and in response to brief handling. Neurosci Lett 393:243-8
Hao, Joy; Cabeza de Vaca, Soledad; Pan, Yan et al. (2006) Effects of central leptin infusion on the reward-potentiating effect of D-amphetamine. Brain Res 1087:123-33
Pan, Yan; Berman, Yemiliya; Haberny, Sandra et al. (2006) Synthesis, protein levels, activity, and phosphorylation state of tyrosine hydroxylase in mesoaccumbens and nigrostriatal dopamine pathways of chronically food-restricted rats. Brain Res 1122:135-42
Haberny, Sandra L; Carr, Kenneth D (2005) Comparison of basal and D-1 dopamine receptor agonist-stimulated neuropeptide gene expression in caudate-putamen and nucleus accumbens of ad libitum fed and food-restricted rats. Brain Res Mol Brain Res 141:121-7
Haberny, S L; Carr, K D (2005) Food restriction increases NMDA receptor-mediated calcium-calmodulin kinase II and NMDA receptor/extracellular signal-regulated kinase 1/2-mediated cyclic amp response element-binding protein phosphorylation in nucleus accumbens upon D-1 dopamine receptor Neuroscience 132:1035-43
Cabeza de Vaca, Soledad; Krahne, Lisa L; Carr, Kenneth D (2004) A progressive ratio schedule of self-stimulation testing in rats reveals profound augmentation of d-amphetamine reward by food restriction but no effect of a ""sensitizing"" regimen of d-amphetamine. Psychopharmacology (Berl) 175:106-13
Haberny, S L; Berman, Y; Meller, E et al. (2004) Chronic food restriction increases D-1 dopamine receptor agonist-induced phosphorylation of extracellular signal-regulated kinase 1/2 and cyclic AMP response element-binding protein in caudate-putamen and nucleus accumbens. Neuroscience 125:289-98

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