The long term objective of the research program is the understanding of nervous system function as influenced by benzodiazepines and opiates. The immediate aims of the benzodiazepine research are: 1) production of monoclonal antibody to benzodiazepine/GABA/chloride ion channel complex proteins which have been purified using a ligand affinity method. 2) application of these antibodies to purify the individual components of this receptor complex. 3) complete purification of the receptor proteins using HPLC. 4) reconstitution of the receptor complex proteins into nerve cells. 5) use of antisera prepared against the receptor complex to study the neurophysiology and metabolism of this structure in neurons. The significance of this work is derived from the role of this receptor/ion channel as a prominent and widely distributed inhibitory conductance mechanism in the central nervous system. Further, it is the site of action of clinically important drugs, such as the benzodiazepines (i.e., Valium) and barbiturates. With respect to the study of opiate neurobiology, this research will focus upon the potential interaction between opioid peptides and the (putative) acidergic neurotransmitters, glutamate and aspartate, in spinal cord and sensory neurons. This will be achieved with the application of antisera prepared against the amino acids and the enzymes, glutaminase and aspartate aminotransferase, which may serve as markers of acidergic neuronal function. The synthesis, cellular release and immunohistochemical distribution of glycylglutamine, a dipeptide derived from beta-endorphin, will also be studied.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
5R01DA002297-11
Application #
3207251
Study Section
Drug Abuse Biomedical Research Review Committee (DABR)
Project Start
1979-04-01
Project End
1991-11-30
Budget Start
1990-01-01
Budget End
1990-11-30
Support Year
11
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Georgetown University
Department
Type
Schools of Arts and Sciences
DUNS #
049515844
City
Washington
State
DC
Country
United States
Zip Code
20057
Potter, Jennifer Sharpe; Dreifuss, Jessica A; Marino, Elise N et al. (2015) The multi-site prescription opioid addiction treatment study: 18-month outcomes. J Subst Abuse Treat 48:62-9
Weiss, Roger D; Potter, Jennifer Sharpe; Griffin, Margaret L et al. (2014) Reasons for opioid use among patients with dependence on prescription opioids: the role of chronic pain. J Subst Abuse Treat 47:140-5
Griffin, Margaret L; Dodd, Dorian R; Potter, Jennifer S et al. (2014) Baseline characteristics and treatment outcomes in prescription opioid dependent patients with and without co-occurring psychiatric disorder. Am J Drug Alcohol Abuse 40:157-62
Sharpe Potter, Jennifer; Bebarta, Vikhyat S; Marino, Elise N et al. (2014) Pain management and opioid risk mitigation in the military. Mil Med 179:553-8
Potter, Jennifer Sharpe; Marino, Elise N (2013) How to avoid opioid misuse. J Fam Pract 62:S2-7
Fiszman, M L; Borodinsky, L N; Neale, J H (1999) GABA induces proliferation of immature cerebellar granule cells grown in vitro. Brain Res Dev Brain Res 115:1-8
Borodinsky, L N; Fiszman, M L (1998) Extracellular potassium concentration regulates proliferation of immature cerebellar granule cells. Brain Res Dev Brain Res 107:43-8
Charlton, M E; Sweetnam, P M; Fitzgerald, L W et al. (1997) Chronic ethanol administration regulates the expression of GABAA receptor alpha 1 and alpha 5 subunits in the ventral tegmental area and hippocampus. J Neurochem 68:121-7
Ghose, S; Wroblewska, B; Corsi, L et al. (1997) N-acetylaspartylglutamate stimulates metabotropic glutamate receptor 3 to regulate expression of the GABA(A) alpha6 subunit in cerebellar granule cells. J Neurochem 69:2326-35
Tieman, S B; Tieman, D G (1996) N-acetylaspartylglutamate immunoreactivity in human retina. Vision Res 36:941-7

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