PROJECT SUMMARY
Opioid abuse, including abuse of prescription opioid medications, has become a significant
health concern. One concern is that it is associated with an increased likelihood of impulsive
and risky behaviors; these behaviors place individuals at risk of contracting and transmitting
diseases such as HIV/AIDS and at risk of continued drug abuse, which can increase the
chances of dependence and overdose. Although impulsivity is a determinant of substance
abuse, evidence indicates that it also is an outcome of substance abuse (i.e., substance abuse
can produce impulsive and risky behavior). Although pre-clinical research investigating effects
of abused drugs on impulsive and risky behavior has grown recently, there are significant gaps
in our knowledge about the specific behavioral mechanisms involved in those effects. Growing
evidence indicates that impulsive and risky choices are the result of behavioral processes that
contribute to reward value. Less is known about precisely how drugs, particularly opioids, affect
specific dimensions that determine reward value. Reward value is a composite measure of
several dimensions, including its size (magnitude), the delay to its receipt (delay), and the
likelihood that the reward actually will be received (probability). The central hypothesis is that
understanding how drugs affect the specific dimensions of reward value is crucial for
understanding their effects on impulsive and risky behavior. Thus, the overall goal is to utilize
innovative laboratory-animal models to characterize how both acute and chronic exposure to,
and withdrawal from, the prescription opioid oxycodone affect specific reward processes
involved in impulsive and risky behavior. This goal will be accomplished by addressing two
specific aims. 1) Isolate and quantify effects of acute and chronic exposure to and withdrawal
from oxycodone on the specific reward mechanisms of impulsive choice. 2) Isolate and quantify
effects of acute and chronic exposure to and withdrawal from oxycodone on the specific reward
mechanisms of risky choice. This proposal is innovative in that it utilizes specialized
experimental methods that identify the specific reward dimensions involved in oxycodone's
effects on impulsive and risky choices, and employs data-analytic methods to quantify the
relative impact of oxycodone on each reward dimension. The proposed research is significant
because it will provide critical information on the behavioral mechanisms involved in effects of
oxycodone on impulsive and risky behavior that will fill gaps in our current knowledge, help
inform investigations of underlying neurobiological mechanisms, and facilitate the development
therapeutic interventions that are based upon the identified reward mechanisms.