Currently, the abuse of prescription opioid medications is a pervasive problem in the U.S. In addition, co-abuse of opioids and alcohol represents a significant problem from the perspective of increased toxicity and decreased success in treatment. Surprisingly few studies have examined the effects of combined administration of opioids and alcohol in humans, and no clinical studies have examined the reinforcing effects of this combination. The current proposal will systematically screen medications that show promise for treating both opioid and alcohol use disorders (OUD and AUD). The guiding principle is that a medication's effects on positive subjective responses and reinforcing effects are the best laboratory procedures to date in predicting its clinical efficacy.In separate studies, we will test suvorexant (Study 1), oxytocin (Study 2), varenicline (Study 3), and gabapentin (Study 4) for their ability to alter opioid-, alcohol-, and combined opioid/alcohol-mediated responses. Participants in all of the studies will meet DSM-5 criteria for moderate-severe OUD and be physically dependent on opioids. In addition, all participants will meet DSM-5 criteria for moderate-severe AUD, but they will not be physically dependent on alcohol. All of the participants will be maintained on sublingual buprenorphine/naloxone throughout the studies and different doses of suvorexant, oxytocin, varenicline, and gabapentin will be evaluated. Overall, the proposed studies will provide a great deal of information about the safety and clinical utility of buprenorphine/naloxone in combination with each of the test medications for treating co-abuse of opioids and alcohol.

Public Health Relevance

Prescription opioid abuse has become prevalent in the U.S., and while some individuals abuse prescription opioids alone, abuse of opioids in combination with alcohol is common. The purpose of the present proposal is to characterize the ability of suvorexant (Study 1), oxytocin (Study 2), varenicline (Study 3), and gabapentin (Study 4) to alter the abuse liability of oxycodone alone, alcohol alone, and oxycodone in combination with alcohol in buprenorphine/naloxone-maintained research participants. These studies are designed to examine the safety, tolerability, and efficacy of the medication using laboratory models of abuse liability (positive subjective responses, craving, and reinforcing effects as measured by the Multiple Choice Procedure).

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
1R01DA039169-01A1
Application #
9029824
Study Section
Biobehavioral Regulation, Learning and Ethology Study Section (BRLE)
Program Officer
Hampson, Aidan
Project Start
2017-06-15
Project End
2019-05-31
Budget Start
2017-06-15
Budget End
2018-05-31
Support Year
1
Fiscal Year
2017
Total Cost
$631,728
Indirect Cost
$191,788
Name
New York State Psychiatric Institute
Department
Type
Independent Hospitals
DUNS #
167204994
City
New York
State
NY
Country
United States
Zip Code
10032