Naltrexone sensitivity during responding for ethanol.

Information

  • Research Project
  • 6807114
  • ApplicationId
    6807114
  • Core Project Number
    R15AA015147
  • Full Project Number
    1R15AA015147-01
  • Serial Number
    15147
  • FOA Number
    PA-03-53
  • Sub Project Id
  • Project Start Date
    9/10/2004 - 20 years ago
  • Project End Date
    7/31/2005 - 19 years ago
  • Program Officer Name
    EGLI, MARK
  • Budget Start Date
    9/10/2004 - 20 years ago
  • Budget End Date
    7/31/2005 - 19 years ago
  • Fiscal Year
    2004
  • Support Year
    1
  • Suffix
  • Award Notice Date
    9/7/2004 - 20 years ago

Naltrexone sensitivity during responding for ethanol.

[unreadable] DESCRIPTION (provided by applicant): The opioid antagonist naltrexone (NTX) reduces responding for food at similar doses as those that reduce responding for ethanol and the animals become supersensitive to NTX's effects. NTX supersensitivity may contribute to the drug's ability to decrease ethanol consumption. If we explore the behavioral and environmental factors that modulate sensitivity to NTX, then we may develop therapeutic techniques to maximize NTX's effect on ethanol drinking and minimize NTX's effect on other behaviors. The purpose of this proposal is to characterize the behavioral and environmental factors that contribute to NTX supersensitivity as it relates to ethanol consumption. The first specific aim will attempt to establish a dose effect relationship for the development of supersensitivity in rats responding for 10% ethanol. Rats responding for ethanol will receive repeated NTX injections once/week for 8 weeks. Preliminary data suggest that the naltrexone's potency to reduce responding for ethanol will increase over time. The second specific aim will determine whether NTX's effects can become associated with contextual stimuli, which may produce NTX-like effects in the absence of the drug. Rats will receive repeated NTX while responding for ethanol in the presence of an olfactory cue (CS+). A separate cue will be used on saline injection days (CS-). Following an injection procedure similar to the first specific aim, we will test whether the CS+ without NTX decreases responding and whether the CS- attenuates NTX's effect. The third specific aim will test whether repeated NTX enhances extinction of responding to an ethanol-conditioned cue and whether this experience will reduce reinstatement after an ethanol priming injection. Rats will have extended exposure to ethanol paired with a cue. NTX will be given repeatedly when rats are responding for only the cue. Later, the rats' responding will be measured after receiving a priming injection of ethanol. These studies should suggest behavioral and environmental factors that may enhance or attenuate NTX's use in treating human alcoholism [unreadable] [unreadable]

IC Name
NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM
  • Activity
    R15
  • Administering IC
    AA
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    55804
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    273
  • Ed Inst. Type
    SCHOOLS OF ARTS AND SCIENCES
  • Funding ICs
    NIAAA:55804\
  • Funding Mechanism
  • Study Section
    NAL
  • Study Section Name
    Neurotoxicology and Alcohol Study Section
  • Organization Name
    GRAND VALLEY STATE UNIVERSITY
  • Organization Department
    PSYCHOLOGY
  • Organization DUNS
    059692996
  • Organization City
    GRAND RAPIDS
  • Organization State
    MI
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    49504
  • Organization District
    UNITED STATES