The objective of this Program Project Grant is to study the molecular neurobiological mechanisms underlying opiate and cocaine addiction. The program of research contains two major strengths. First, is the multidisciplinary nature of our ongoing and proposed research. Each research area represents an integration of molecular, biochemical, electrophysiological, neuropharmacological, and behavioral levels of analysis aimed at our basic research with a well-established clinical research program in drug abuse in our research group. The Program Project Grant is organized into a small Administrative Core, two scientific Cores, and five Projects. The transgenic Core is responsible for the breeding of may types of transgenic and knock out mice, and constructs for viral-mediated gene transfer, to be utilized in the proposed research. The Core is also responsible for the construction of several new lines of mutant mice, including those with inducible tissue-specific transgenes. The Behavioral Core is responsible for analysis of relatively routine drug-relative behaviors, including opiate withdrawal, locomotor activity, and place conditioning, in both rats and mice. Project 1 is a continuation of a productive and collaborative effort among several laboratories to study the molecular and cellular mechanisms by which opiates regulate locus coeruleus neurons and to relate these changes to behavioral measures of opiate withdrawal. Project 2 is a continuation of related collaborative studies that focus on molecular and cellular actions on opiates and cocaine in several other target brain regions, including dorsal raphe, prefrontal cortex, and lateral septum. Project 3 is a continuation of collaborative molecular, cellular, and behavioral studies of the role of specific neuropeptide receptors in the long-term actions of opiates and cocaine on specific target brain regions. Project 4 is a continuation of efforts to study the functional role by known molecular and cellular responses to drugs of abuse in the mesolimbic dopamine system. Animal models of drug reinforcement and craving, in conjunction with transgenic and viral-mediated gene transfer methods, will be used. Project 5 is a new effort to examine the genetic contributions to drug abuse in people. This work is an ideal way of applying fundamental knowledge arising from the basic Projects to clinical populations. Renewal of the Program Project Grant will enable continuation, and further strengthening, of our multidisciplinary research program into the molecular neurobiological mechanisms underlying drug addiction.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Program Projects (P01)
Project #
5P01DA008227-08
Application #
6175787
Study Section
Human Development Research Subcommittee (NIDA)
Program Officer
Pollock, Jonathan D
Project Start
1993-08-01
Project End
2000-12-31
Budget Start
2000-07-15
Budget End
2000-12-31
Support Year
8
Fiscal Year
2000
Total Cost
$533,365
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Psychiatry
Type
Schools of Medicine
DUNS #
City
Dallas
State
TX
Country
United States
Zip Code
75390
Hamilton, Peter J; Burek, Dominika J; Lombroso, Sonia I et al. (2018) Cell-Type-Specific Epigenetic Editing at the Fosb Gene Controls Susceptibility to Social Defeat Stress. Neuropsychopharmacology 43:272-284
Egervari, Gabor; Kozlenkov, Alexey; Dracheva, Stella et al. (2018) Molecular windows into the human brain for psychiatric disorders. Mol Psychiatry :
de la Fuente Revenga, Mario; Ibi, Daisuke; Saunders, Justin M et al. (2018) HDAC2-dependent Antipsychotic-like Effects of Chronic Treatment with the HDAC Inhibitor SAHA in Mice. Neuroscience 388:102-117
Anderson, Ethan M; Sun, Haosheng; Guzman, Daniel et al. (2018) Knockdown of the histone di-methyltransferase G9a in nucleus accumbens shell decreases cocaine self-administration, stress-induced reinstatement, and anxiety. Neuropsychopharmacology :
Hamilton, Peter J; Lim, Carissa J; Nestler, Eric J et al. (2018) Stereotaxic Surgery and Viral Delivery of Zinc-Finger Epigenetic Editing Tools in Rodent Brain. Methods Mol Biol 1867:229-238
Inquimbert, Perrine; Moll, Martin; Latremoliere, Alban et al. (2018) NMDA Receptor Activation Underlies the Loss of Spinal Dorsal Horn Neurons and the Transition to Persistent Pain after Peripheral Nerve Injury. Cell Rep 23:2678-2689
Ayata, Pinar; Badimon, Ana; Strasburger, Hayley J et al. (2018) Epigenetic regulation of brain region-specific microglia clearance activity. Nat Neurosci 21:1049-1060
Walker, Deena M; Nestler, Eric J (2018) Neuroepigenetics and addiction. Handb Clin Neurol 148:747-765
Li, Xuan; Carreria, Maria B; Witonsky, Kailyn R et al. (2018) Role of Dorsal Striatum Histone Deacetylase 5 in Incubation of Methamphetamine Craving. Biol Psychiatry 84:213-222
Anderson, Ethan M; Larson, Erin B; Guzman, Daniel et al. (2018) Overexpression of the Histone Dimethyltransferase G9a in Nucleus Accumbens Shell Increases Cocaine Self-Administration, Stress-Induced Reinstatement, and Anxiety. J Neurosci 38:803-813

Showing the most recent 10 out of 312 publications