Marijuana is the most frequently abused illegal drug in the U.S., particularly among young people. The widespread abuse of marijuana continues despite the clear documentation that this is associated with adverse effects. This R21 proposal is driven by our desire to conduct coordinated PET and neuropsychological studies of the relationships between the kinetics of entry into and initial clearance from the brain of (-)-delta-9-tetrahydrocannabinol (THC), the major active ingredient of cannabis smoke, and the subjective and physiological effects of this drug in individual human subjects. We hypothesize that, as with other abused substances, its rewarding potency depends on the rate of entry into4cthe brain. These studies require the labeling of THC with carbon-I I, a nuclide with half-life of 20 minutes, whose concentration can be measured in the human body using positron emission tomography. Our group has extensive experience in the synthesis of novel positron emitting tracers including many carbon-I I labeled compounds and a fluorine-18 labeled analog of delta-8 THC (a biologically active isomer of delta-9-THC that is a minor constituent of cannabis). Our prior studies also include the synthesis and biological evaluation of several agonist and antagonist radioligands that bind to the brain cannabinoid (CBI) receptor in vivo. However, the rapid synthesis of carbon-I I labeled delta-9-THC presents some technical challenges that are expected to require approximately two years to solve, and trial of several approaches that are detailed in this proposal. It should be noted that, based on our experience with several CBI receptor radioligands of higher affinity and lower lipophilicity than THC, we do not expect that carbon-I I labeled delta-9-THC will have good properties for imaging the distribution of this receptor. Rather, the purpose of preparing carbon-I I labeled delta-9- is to study the regional brain pharmacokinetics of this drug after intravenous administration to human subjects.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21DA015545-01
Application #
6535439
Study Section
Molecular, Cellular and Developmental Neurosciences 2 (MDCN)
Program Officer
Rapaka, Rao
Project Start
2002-08-01
Project End
2004-07-31
Budget Start
2002-08-01
Budget End
2003-07-31
Support Year
1
Fiscal Year
2002
Total Cost
$141,178
Indirect Cost
Name
Brookhaven National Laboratory
Department
Type
DUNS #
027579460
City
Upton
State
NY
Country
United States
Zip Code
11973
Gatley, S John; Volkow, Nora D; Wang, Gene-Jack et al. (2005) PET imaging in clinical drug abuse research. Curr Pharm Des 11:3203-19