Methamphetamine-alcohol interactions in murine models of sequential and simultaneous oral drug-taking.

TitleMethamphetamine-alcohol interactions in murine models of sequential and simultaneous oral drug-taking.
Publication TypeJournal Article
Year of Publication2017
AuthorsFultz EK, Martin DL, Hudson CN, Kippin TE, Szumlinski KK
JournalDrug Alcohol Depend
Volume177
Pagination178-186
Date Published2017 08 01
ISSN1879-0046
KeywordsAdministration, Oral, Alcohol Drinking, Amphetamine-Related Disorders, Animals, Choice Behavior, Conditioning, Operant, Disease Models, Animal, Drug Interactions, Ethanol, Female, Male, Methamphetamine, Mice, Mice, 129 Strain, Mice, Inbred C57BL, Self Administration
Abstract

BACKGROUND: A high degree of co-morbidity exists between methamphetamine (MA) addiction and alcohol use disorders and both sequential and simultaneous MA-alcohol mixing increases risk for co-abuse. As little preclinical work has focused on the biobehavioral interactions between MA and alcohol within the context of drug-taking behavior, we employed simple murine models of voluntary oral drug consumption to examine how prior histories of either MA- or alcohol-taking influence the intake of the other drug.

METHODS: In one study, mice with a 10-day history of binge alcohol-drinking [5,10, 20 and 40% (v/v); 2h/day] were trained to self-administer oral MA in an operant-conditioning paradigm (10-40mg/L). In a second study, mice with a 10-day history of limited-access oral MA-drinking (5, 10, 20 and 40mg/L; 2h/day) were presented with alcohol (5-40% v/v; 2h/day) and then a choice between solutions of 20% alcohol, 10mg/L MA or their mix.

RESULTS: Under operant-conditioning procedures, alcohol-drinking mice exhibited less MA reinforcement overall, than water controls. However, when drug availability was not behaviorally-contingent, alcohol-drinking mice consumed more MA and exhibited greater preference for the 10mg/L MA solution than drug-naïve and combination drug-experienced mice. Conversely, prior MA-drinking history increased alcohol intake across a range of alcohol concentrations.

DISCUSSION: These exploratory studies indicate the feasibility of employing procedurally simple murine models of sequential and simultaneous oral MA-alcohol mixing of relevance to advancing our biobehavioral understanding of MA-alcohol co-abuse.

DOI10.1016/j.drugalcdep.2017.03.026
Alternate JournalDrug Alcohol Depend
PubMed ID28601731
Grant ListR01 AA024044 / AA / NIAAA NIH HHS / United States
R01 DA039168 / DA / NIDA NIH HHS / United States