Alcoholism is a multifaceted disease with many different etiologies. This probably explains why no single approach to treatment has been universally successful. Clearly, more research is needed. The Medical University of South Carolina (MUSC) is uniquely qualified to fulfill this need, but it requires the resources provided by an Alcohol Research Center (ARC) in order to realize its potential. A Center mechanism permits an institution to embark on a thematic research program by providing an infrastructure which encourages a blending of scientific talents. While clinical research is the most common treatment research approach, advances are more likely to be achieved when clinical research is complemented by animal research. This application for an ARC at MUSC has afforded the opportunity to bring the disciplines of psychiatry and experimental psychology together along the treatment research theme. A total of five research components are proposed, along with four core components that support the research infrastructure, the ARC's education/training mission, or provide support for three pilot projects from young psychiatric researchers. The thread that ties all the research components together is pharmacotherapy. Psychiatric comorbidity represents a secondary area of expertise as well as research interest of some of the faculty. The thematic approach of the proposed ARC is a multidisciplinary one. The projects are interdigitated. Research components #2 and #4 involve medical management of alcohol withdrawal in humans and animals, respectively. Research components 1, #3, and #5 involve evaluation of pharmacologic agents that affect the serotonin and/or opiate systems in humans, or animals, respectively. The approaches and models being employed are applicable to studies of other agents, as well. Thus, the MUSC ARC would be well positioned to evaluate compounds first in animal models, and then in clinical trials. Such an integrated and concerted """"""""bench-to- clinic"""""""" strategy is certainly needed toward achieving the ultimate goal of developing and successfully implementing effective treatment. Further, it is likely that the best therapy will be derived from multidisciplinary and interdisciplinary approaches, and not just from medications alone. Given that matching patients to treatments based on individual psychological or psychiatric characteristics may have more promise than standard homogeneous approaches to improve treatment outcome, it seems like a Center with focused basic and clinical research in this area is sorely needed. MUSC has the dedicated research talent, administrative support, and physical space to be such a Center.

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Specialized Center (P50)
Project #
5P50AA010761-02
Application #
2000553
Study Section
Special Emphasis Panel (SRCA (60))
Project Start
1995-12-10
Project End
2000-11-30
Budget Start
1996-12-01
Budget End
1997-11-30
Support Year
2
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Medical University of South Carolina
Department
Psychiatry
Type
Schools of Medicine
DUNS #
183710748
City
Charleston
State
SC
Country
United States
Zip Code
29425
Hanlon, Colleen A; Dowdle, Logan T; Henderson, J Scott (2018) Modulating Neural Circuits with Transcranial Magnetic Stimulation: Implications for Addiction Treatment Development. Pharmacol Rev 70:661-683
Hanlon, Colleen A; Dowdle, Logan T; Gibson, Nicole B et al. (2018) Cortical substrates of cue-reactivity in multiple substance dependent populations: transdiagnostic relevance of the medial prefrontal cortex. Transl Psychiatry 8:186
Gioia, Dominic A; Xu, Minfu; Wayman, Wesley N et al. (2018) Effects of drugs of abuse on channelrhodopsin-2 function. Neuropharmacology 135:316-327
Anton, Raymond F; Latham, Patricia K; Voronin, Konstantin E et al. (2018) Nicotine-Use/Smoking Is Associated with the Efficacy of Naltrexone in the Treatment of Alcohol Dependence. Alcohol Clin Exp Res 42:751-760
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
Osterndorff-Kahanek, Elizabeth A; Tiwari, Gayatri R; Lopez, Marcelo F et al. (2018) Long-term ethanol exposure: Temporal pattern of microRNA expression and associated mRNA gene networks in mouse brain. PLoS One 13:e0190841
Stewart, Scott H; Reuben, Adrian; Anton, Raymond F (2018) Reply: Carbohydrate Deficient Transferrin in Patients with Cirrhosis: A Tale of Bridges. Alcohol Alcohol 53:351-352
Kearney-Ramos, Tonisha E; Lench, Daniel H; Hoffman, Michaela et al. (2018) Gray and white matter integrity influence TMS signal propagation: a multimodal evaluation in cocaine-dependent individuals. Sci Rep 8:3253
Haun, Harold L; Griffin, William C; Lopez, Marcelo F et al. (2018) Increasing Brain-Derived Neurotrophic Factor (BDNF) in medial prefrontal cortex selectively reduces excessive drinking in ethanol dependent mice. Neuropharmacology 140:35-42
Schacht, Joseph P; Voronin, Konstantin E; Randall, Patrick K et al. (2018) Dopaminergic Genetic Variation Influences Aripiprazole Effects on Alcohol Self-Administration and the Neural Response to Alcohol Cues in a Randomized Trial. Neuropsychopharmacology 43:1247-1256

Showing the most recent 10 out of 209 publications