BEHAVIORAL EVALUATION OF NOVEL DAT ANTAGONIST

Information

  • Research Project
  • 6140845
  • ApplicationId
    6140845
  • Core Project Number
    R41DA012839
  • Full Project Number
    1R41DA012839-01A1
  • Serial Number
    12839
  • FOA Number
  • Sub Project Id
  • Project Start Date
    4/15/2000 - 24 years ago
  • Project End Date
    3/31/2001 - 23 years ago
  • Program Officer Name
    PATEL, AMRAT
  • Budget Start Date
    4/15/2000 - 24 years ago
  • Budget End Date
    3/31/2001 - 23 years ago
  • Fiscal Year
    2000
  • Support Year
    1
  • Suffix
    A1
  • Award Notice Date
    4/6/2000 - 24 years ago

BEHAVIORAL EVALUATION OF NOVEL DAT ANTAGONIST

DESCRIPTION (Adapted from the application): The goal of this Phase I study is to develop anti-cocaine drugs that curb cocaine's euphoria and craving. The selection criteria are that the drugs cannot be addictive themselves, nor can they produce an impairment of normal hedonic function. It is felt that drugs with these actions will be found among compounds that displace cocaine from dopamine transporter without affecting dopamine uptake per se. The approach will be to screen novel monoamine transporter ligands for hedonic and anti-cocaine actions using the Brain Stimulation Reward (BSR) curve shift paradigm. This behavioral test has a number of unique features including the ability to distinguish hedonically positive or neutral drugs from compounds with negatively hedonic actions. Behavioral results will be used to define the optimal neurochemical actions of the drugs vis-a-vis monoamine transporters. The last specific aim is to develop an animal model of craving based on IVSA reinstatement paradigm with a peripheral injection as the cue. The two series of drugs to be examined are the diphenylmethoxypiperazines (specific GBR analogs; the Nocaine-A series) that are partial cocaine agonists and a series of disubstituted piperidines (the Nocaine-B series). PROPOSED COMMERCIAL APPLICATION: NOT AVAILABLE

IC Name
NATIONAL INSTITUTE ON DRUG ABUSE
  • Activity
    R41
  • Administering IC
    DA
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    86025
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    279
  • Ed Inst. Type
  • Funding ICs
    NIDA:86025\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    BIOSTREAM THERAPEUTICS, INC.
  • Organization Department
  • Organization DUNS
  • Organization City
    CAMBRIDGE
  • Organization State
    MA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    02142
  • Organization District
    UNITED STATES