Understanding Cannabis Withdrawal: A PET Study of Endocannabinoid Metabolism

Information

  • Research Project
  • 9742446
  • ApplicationId
    9742446
  • Core Project Number
    R21DA045296
  • Full Project Number
    5R21DA045296-02
  • Serial Number
    045296
  • FOA Number
    PA-16-161
  • Sub Project Id
  • Project Start Date
    7/15/2018 - 6 years ago
  • Project End Date
    6/30/2020 - 4 years ago
  • Program Officer Name
    HILLERY, PAUL
  • Budget Start Date
    7/1/2019 - 5 years ago
  • Budget End Date
    6/30/2020 - 4 years ago
  • Fiscal Year
    2019
  • Support Year
    02
  • Suffix
  • Award Notice Date
    6/19/2019 - 5 years ago

Understanding Cannabis Withdrawal: A PET Study of Endocannabinoid Metabolism

PROJECT SUMMARY Cannabis is currently the most used drug in the US, particularly in young people. It is also associated with the highest demand for intervention; however, current treatment success rates are low, with 70% of motivated treatment-seekers relapsing early, during the withdrawal phase (< 3 weeks from last use). Cannabis withdrawal, a clinically recognized but poorly understood syndrome, is a risk factor for relapse and a target for intervention. There are currently no approved pharmacotherapies for cannabis use disorder (CUD), while a severe deficit exists in understanding the neurobiology of cannabis withdrawal syndrome. Preclinical and human genetic studies have implicated Fatty Acid Amide Hydrolase (FAAH), the enzyme metabolizing the major endocannabinoid anandamide in cannabis withdrawal, suggesting that higher metabolic activity (i.e.: lower anandamide) may be associated with greater withdrawal symptomatology and that increasing endocannabinoids may decrease the severity of cannabis withdrawal. In our NIH-funded pilot study we found that levels of this enzyme are low in CUD after overnight cannabis cessation (12 hours) and relate to levels of cannabis metabolites. Thus, we propose that low levels of FAAH during early abstinence act to delay the appearance of withdrawal and that as levels increase, symptomatology manifests. Our data indicate the need for scanning subjects during acute withdrawal in order to understand how FAAH contributes to cannabis withdrawal and, by extension, to relapse. We are uniquely suited to investigate the role of FAAH in CUD and cannabis withdrawal as we have collected preliminary data in this condition; we have the clinical and scientific expertise in the field of CUD and imaging and have the only available neuroimaging tool to investigate this question. There is an urgent need to accelerate the translation, into clinic, of pharmacotherapies already in development, by providing neuroimaging information which could advance our understanding of endocannabinoid metabolism in CUD. Following up on our finding of decreased FAAH activity in CUD during early abstinence, our major specific aim is to establish, by PET imaging, whether FAAH levels increase during acute withdrawal (from overnight to 72 hours) and are associated with clinical symptoms. The potential impact of this project is important, as it provides the first imaging investigation of endocannabinoid metabolism during cannabis withdrawal. The knowledge generated by this project will provide the basis for the further development of evidence-based therapeutic approaches targeting FAAH.

IC Name
NATIONAL INSTITUTE ON DRUG ABUSE
  • Activity
    R21
  • Administering IC
    DA
  • Application Type
    5
  • Direct Cost Amount
    138522
  • Indirect Cost Amount
    11082
  • Total Cost
    149604
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    279
  • Ed Inst. Type
  • Funding ICs
    NIDA:149604\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    NPAS
  • Study Section Name
    Neural Basis of Psychopathology, Addictions and Sleep Disorders Study Section
  • Organization Name
    CENTRE FOR ADDICTION AND MENTAL HEALTH
  • Organization Department
  • Organization DUNS
    207855271
  • Organization City
    TORONTO
  • Organization State
    ON
  • Organization Country
    CANADA
  • Organization Zip Code
    M5S2S1
  • Organization District
    CANADA