Methamphetamine dependence is a significant public-health concern. The results of clinical trials suggest that agonist replacement therapies (e.g., d-amphetamine) may be effective for methamphetamine dependence. The present project has three specific aims. The first specific aim is to demonstrate the safety, tolerability and behavioral effects of intranasal methamphetamine in humans maintained on d-amphetamine. To accomplish this aim, we will conduct one experiment in which non-treatment seeking volunteers with recent histories of illicit stimulant use will receive ascending doses of intranasal methamphetamine while maintained on increasing doses of d-amphetamine (Exp. 1). Cardiovascular indices will be used to determine the safety and tolerability of the d-amphetamine-methamphetamine combinations while subjective-effect questionnaires will be used to characterize the behavioral effects. The results of this experiment will guide the selection of doses to be tested in subsequent studies. The second specific aim is to demonstrate that d-amphetamine maintenance attenuates the reinforcing effects of methamphetamine. To accomplish this aim, we will determine the reinforcing effects of intranasal methamphetamine during d-amphetamine maintenance using a progressive-ratio procedure (Exp. 2). Pharmacotherapies that attenuate the reinforcing effects of methamphetamine may be effective for initiating abstinence. The third specific aim is to demonstrate that d-amphetamine maintenance attenuates the discriminative-stimulus effects of methamphetamine. To accomplish this aim, volunteers will learn to discriminate intranasal methamphetamine (Exp. 3). The discriminative effects of methamphetamine may be involved in relapse to drug-taking behavior in that an initial dose (i.e., a lapse) may function as a discriminative stimulus signaling the availability of more drug. Pharmacotherapies that attenuate the discriminative-stimulus effects of methamphetamine may be effective for preventing relapse. The proposed research will provide important additional clinical information regarding the efficacy of agonist replacement therapies for methamphetamine dependence. By using two sophisticated human laboratory procedures, one to model abstinence initiation (i.e., drug self-administration) and the other to model relapse prevention (i.e., drug discrimination), the proposed research will determine the mechanisms that mediate the clinical efficacy of d-amphetamine for methamphetamine dependence. By inference, then, the proposed research will identify the optimal conditions under which d-amphetamine would be effective as a pharmacotherapy for methamphetamine dependence (i.e., initiate abstinence or prevent relapse). Finally, because d-amphetamine reduces methamphetamine use, these clinical findings can be used as a reference to determine the predictive validity of human laboratory procedures. Identifying procedures for assessing the efficacy of putative pharmacotherapies via a """"""""beside-to-bench"""""""" or """"""""reverse engineering"""""""" strategy is important because human laboratory studies can be conducted more rapidly and efficiently than clinical trials.

Public Health Relevance

Methamphetamine dependence is a significant public health concern. The proposed research will provide important clinical information regarding the efficacy of agonist replacement therapy for methamphetamine dependence. The proposed research will also identify the optimal conditions under which d-amphetamine would be effective as a pharmacotherapy for methamphetamine dependence (i.e., initiate abstinence or prevent relapse). Finally, the proposed research will determine appropriate human laboratory procedures for testing pharmacotherapies for methamphetamine dependence. Identifying appropriate human laboratory procedures for assessing the efficacy of pharmacotherapies for methamphetamine dependence is important because laboratory studies can be conducted more rapidly and efficiently than clinical trials.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
5R01DA025032-02
Application #
7754132
Study Section
Special Emphasis Panel (ZDA1-MXH-H (20))
Program Officer
Oversby, Steven
Project Start
2009-01-01
Project End
2013-12-31
Budget Start
2010-01-01
Budget End
2010-12-31
Support Year
2
Fiscal Year
2010
Total Cost
$362,588
Indirect Cost
Name
University of Kentucky
Department
Psychology
Type
Schools of Medicine
DUNS #
939017877
City
Lexington
State
KY
Country
United States
Zip Code
40506
Rice, Beth Ann; Eaton, Shannon E; Prendergast, Mark A et al. (2018) A glucocorticoid receptor antagonist reduces sign-tracking behavior in male Japanese quail. Exp Clin Psychopharmacol 26:329-334
Alcorn 3rd, Joseph L; Pike, Erika; Stoops, William S et al. (2017) A pilot investigation of acute inhibitory control training in cocaine users. Drug Alcohol Depend 174:145-149
Strickland, Justin C; Lile, Joshua A; Rush, Craig R et al. (2016) Comparing exponential and exponentiated models of drug demand in cocaine users. Exp Clin Psychopharmacol 24:447-455
Pike, Erika; Stoops, William W; Rush, Craig R (2016) Acute buspirone dosing enhances abuse-related subjective effects of oral methamphetamine. Pharmacol Biochem Behav 150-151:87-93
Strickland, Justin C; Bolin, B Levi; Lile, Joshua A et al. (2016) Differential sensitivity to learning from positive and negative outcomes in cocaine users. Drug Alcohol Depend 166:61-8
Bolin, B Levi; Stoops, William W; Sites, Jeremy P et al. (2016) Abuse Potential of Oral Phendimetrazine in Cocaine-dependent Individuals: Implications for Agonist-like Replacement Therapy. J Addict Med 10:156-65
Marks, Katherine R; Alcorn 3rd, Joseph L; Stoops, William W et al. (2016) Cigarette Cue Attentional Bias in Cocaine-Smoking and Non-Cocaine-Using Cigarette Smokers. Nicotine Tob Res 18:1915-9
Strickland, Justin C; Wagner, Frances P; Stoops, William W et al. (2015) Profile of internet access in active cocaine users. Am J Addict 24:582-5
Stoops, William W; Pike, Erika; Hays, Lon R et al. (2015) Naltrexone and bupropion, alone or combined, do not alter the reinforcing effects of intranasal methamphetamine. Pharmacol Biochem Behav 129:45-50
Pike, Erika; Marks, Katherine R; Stoops, William W et al. (2015) Cocaine-related stimuli impair inhibitory control in cocaine users following short stimulus onset asynchronies. Addiction 110:1281-6

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