The Alcohol Research Center of The Scripps Research Institute (TRSI-ARC) aims at continuing its interdisciplinary program focused on the theme of the central nervous system effects of alcohol. For this renewal application, the TSRI-ARC will be a P60 consisting of 10 components and an Educational Component. Four Core components are proposed: Administrative, Animal Models Development, Biochemical, Clinical, and Pilot. Five research components are proposed: Cellular Neurobiology (Siggins), Neuroendocrinology (Rivier), Neuropharmacology(Weiss), Clinical Neurobehavioral (Ehlers), and Clinical Neurophysiology (Polich).The TRSI-ARC research program will employ molecular, cellular, neuropharmacological and clinical research methods on Experimental animal subjects and human subjects. The overall hypothesis of the TSRI-ARC is that the function of specific neurotransmitter synapses in select parts of the reward and stress systems that are compromised by chronic ethanol administration account for the development of vulnerability to alcoholism in genetically prone individuals. Three major subthemes have emerged from our present research: 1) the neuropharrnacological mechanisms of vulnerability to dependence by identifying how specific brain reward and stress circuits change during the development of alcohol dependence, 2) the neuropharmacological changes that persist during protracted abstinence eventually leading to relapse to heavy drinking and 3) the neuropharmacological changes in reward and stress mechanisms that are responsible for the individual differences associated with a risk for development of dependence. Progress during the previous funding period has led to a focus on understanding dependence-induced neuroadaptive mechanisms involving corticotropin-releasing factor and neuropeptide Y systems and modulatory systems such as neuroactive steroids and endocannabinoids. Residual allostatic changes in the brain reward and stress neurocircuitry that persist following acute abstinence are envisioned as a crucial part of the basis for inheritable susceptibility to human alcoholism. The TSRI-ARC also supports the Center at Large which includes: 14 NIAAA, R01's, 1 NIAAA R23, 2 NIAAA K awards, 1 NIAAA training grant, and 2 NIAAA consortium core components. Training and information dissemination to the San Diego community will be effected by the training opportunities of the Center including an NIAAA training grant and the Education Component.

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Comprehensive Center (P60)
Project #
5P60AA006420-23
Application #
7002764
Study Section
Special Emphasis Panel (ZAA1-AA (04))
Program Officer
Egli, Mark
Project Start
1983-12-01
Project End
2007-12-31
Budget Start
2006-01-01
Budget End
2006-12-31
Support Year
23
Fiscal Year
2006
Total Cost
$2,006,914
Indirect Cost
Name
Scripps Research Institute
Department
Type
DUNS #
781613492
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Kreisler, A D; Mattock, M; Zorrilla, E P (2018) The duration of intermittent access to preferred sucrose-rich food affects binge-like intake, fat accumulation, and fasting glucose in male rats. Appetite 130:59-69
Varodayan, F P; Khom, S; Patel, R R et al. (2018) Role of TLR4 in the Modulation of Central Amygdala GABA Transmission by CRF Following Restraint Stress. Alcohol Alcohol 53:642-649
McClatchy, Daniel B; Yu, Nam-Kyung; Martínez-Bartolomé, Salvador et al. (2018) Structural Analysis of Hippocampal Kinase Signal Transduction. ACS Chem Neurosci :
Berger, Anthony L; Henricks, Angela M; Lugo, Janelle M et al. (2018) The Lateral Habenula Directs Coping Styles Under Conditions of Stress via Recruitment of the Endocannabinoid System. Biol Psychiatry 84:611-623
Mason, Barbara J; Quello, Susan; Shadan, Farhad (2018) Gabapentin for the treatment of alcohol use disorder. Expert Opin Investig Drugs 27:113-124
Varodayan, Florence P; Sidhu, Harpreet; Kreifeldt, Max et al. (2018) Morphological and functional evidence of increased excitatory signaling in the prelimbic cortex during ethanol withdrawal. Neuropharmacology 133:470-480
Matzeu, Alessandra; Martin-Fardon, Rémi (2018) Drug Seeking and Relapse: New Evidence of a Role for Orexin and Dynorphin Co-transmission in the Paraventricular Nucleus of the Thalamus. Front Neurol 9:720
Sidhu, Harpreet; Kreifeldt, Max; Contet, Candice (2018) Affective Disturbances During Withdrawal from Chronic Intermittent Ethanol Inhalation in C57BL/6J and DBA/2J Male Mice. Alcohol Clin Exp Res 42:1281-1290
Ehlers, Cindy L; Wills, Derek; Gilder, David A (2018) A history of binge drinking during adolescence is associated with poorer sleep quality in young adult Mexican Americans and American Indians. Psychopharmacology (Berl) 235:1775-1782
Pavon, Francisco J; Serrano, Antonia; Sidhpura, Nimish et al. (2018) Fatty acid amide hydrolase (FAAH) inactivation confers enhanced sensitivity to nicotine-induced dopamine release in the mouse nucleus accumbens. Addict Biol 23:723-734

Showing the most recent 10 out of 211 publications