TY - JOUR
T1 - Intermittent ethanol access schedule in rats as a preclinical model of alcohol abuse
AU - Carnicella, Sebastien
AU - Ron, Dorit
AU - Barak, Segev
N1 - Funding Information:
This review was supported by NIH/NIAAA P50 AA017072 , NIH/NIAAA R01 AA016848, NIH/NIAAA R01 AA014366 and NIH/NIAAA R01 AA013438 (D.R.), and by the Israel Science Foundation (ISF) grants No. 968-13 and 1916-13 (S.B.). The authors thank Mr. Oren Even-Chen for his assistance in preparing the manuscript.
PY - 2014/5
Y1 - 2014/5
N2 - One of the major challenges in preclinical studies of alcohol abuse and dependence remains the development of paradigms that will elicit high ethanol intake and mimic the progressive transition from low or moderate social drinking to excessive alcohol consumption. Exposure of outbred rats to repeated cycles of free-choice ethanol intake and withdrawal with the use of intermittent access to 20% ethanol in a 2-bottle choice procedure (IA2BC) has been shown to induce a gradual escalation of voluntary ethanol intake and preference, eventually reaching ethanol consumption levels of 5-6 g/kg/24 h, and inducing pharmacologically relevant blood ethanol concentrations (BECs). This procedure has recently been gaining popularity due to its simplicity, high validity, and reliable outcomes. Here we review experimental and methodological data related to IA2BC, and discuss the usefulness and advantages of this procedure as a valuable pre-training method for initiating operant ethanol self-administration of high ethanol intake, as well as conditioned place preference (CPP). Despite some limitations, we provide evidence that IA2BC and related operant procedures provide the possibility to operationalize multiple aspects of alcohol abuse and addiction in a rat model, including transition from social-like drinking to excessive alcohol consumption, binge drinking, alcohol seeking, relapse, and neuroadaptations related to excessive alcohol intake. Hence, IA2BC appears to be a useful and relevant procedure for preclinical evaluation of potential therapeutic approaches against alcohol abuse disorders.
AB - One of the major challenges in preclinical studies of alcohol abuse and dependence remains the development of paradigms that will elicit high ethanol intake and mimic the progressive transition from low or moderate social drinking to excessive alcohol consumption. Exposure of outbred rats to repeated cycles of free-choice ethanol intake and withdrawal with the use of intermittent access to 20% ethanol in a 2-bottle choice procedure (IA2BC) has been shown to induce a gradual escalation of voluntary ethanol intake and preference, eventually reaching ethanol consumption levels of 5-6 g/kg/24 h, and inducing pharmacologically relevant blood ethanol concentrations (BECs). This procedure has recently been gaining popularity due to its simplicity, high validity, and reliable outcomes. Here we review experimental and methodological data related to IA2BC, and discuss the usefulness and advantages of this procedure as a valuable pre-training method for initiating operant ethanol self-administration of high ethanol intake, as well as conditioned place preference (CPP). Despite some limitations, we provide evidence that IA2BC and related operant procedures provide the possibility to operationalize multiple aspects of alcohol abuse and addiction in a rat model, including transition from social-like drinking to excessive alcohol consumption, binge drinking, alcohol seeking, relapse, and neuroadaptations related to excessive alcohol intake. Hence, IA2BC appears to be a useful and relevant procedure for preclinical evaluation of potential therapeutic approaches against alcohol abuse disorders.
KW - Animal models
KW - Binge drinking
KW - Blood ethanol concentrations
KW - Ethanol
KW - Excessive drinking
KW - Intermittent access
KW - Neuroadaptations
KW - Operant self-administration
KW - Relapse
KW - Two-bottle choice
UR - http://www.scopus.com/inward/record.url?scp=84899926997&partnerID=8YFLogxK
U2 - 10.1016/j.alcohol.2014.01.006
DO - 10.1016/j.alcohol.2014.01.006
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C2 - 24721195
AN - SCOPUS:84899926997
SN - 0741-8329
VL - 48
SP - 243
EP - 252
JO - Alcohol
JF - Alcohol
IS - 3
ER -