Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2010 Feb;44(1):67-80.
doi: 10.1016/j.alcohol.2009.09.034.

Alcohol response and consumption in adolescent rhesus macaques: life history and genetic influences

Affiliations
Review

Alcohol response and consumption in adolescent rhesus macaques: life history and genetic influences

Melanie L Schwandt et al. Alcohol. 2010 Feb.

Abstract

The use of alcohol by adolescents is a growing problem and has become an important research topic in the etiology of the alcohol use disorders. A key component of this research has been the development of animal models of adolescent alcohol consumption and alcohol response. Because of their extended period of adolescence, rhesus macaques are especially well suited for modeling alcohol-related phenotypes that contribute to the adolescent propensity for alcohol consumption. In this review, we discuss studies from our laboratory that have investigated both the initial response to acute alcohol administration and the consumption of alcohol in voluntary self-administration paradigms in adolescent rhesus macaques. These studies confirm that adolescence is a time of dynamic change both behaviorally and physiologically, and that alcohol response and alcohol consumption are influenced by life history variables, such as age, sex, and adverse early experience in the form of peer-rearing. Furthermore, genetic variants that alter functioning of the serotonin, endogenous opioid, and corticotropin-releasing hormone systems are shown to influence both physiological and behavioral outcomes, in some cases interacting with early experience to indicate gene by environment interactions. These findings highlight several of the pathways involved in alcohol response and consumption, namely reward, behavioral dyscontrol, and vulnerability to stress, and demonstrate a role for these pathways during the early stages of alcohol exposure in adolescence.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Lack of an effect of early exposure to alcohol on later alcohol consumption. Subjects (n = 53) were tested in the social group condition for 1 hour a day, five days a week, for 4 weeks when they were 4-5 years of age. A subset of subjects (n = 30) had been similarly tested in the single cage condition when they were about 2.5 years of age. Analysis was performed using repeated measures ANOVA, with testing week as the within subjects variable and sex and early exposure (yes/no) as the between subjects variables. Precise age at the time of testing in the social group was also included as a covariate. Data are presented as mean (± SEM) alcohol consumption for each testing week. There was no main effect of sex F(1,48) = 3.91; P = 0.06 and no main effect of early exposure F(1,48) = 0.72; P = 0.40, nor any interactive effects of early exposure with sex F(1,48) = 0.04; P = 0.84 or with week of testing F(3, 144) = 0.11; P = 0.95.
Figure 2
Figure 2
Rearing condition influences alcohol intake in the single cage but not the social group setting. Data on 211 monkeys from the limited-access, voluntary self-administration paradigm were analyzed using 2-way ANOVA, with rearing history, sex, and testing condition as independent variables and mean alcohol consumption (g/kg) across testing weeks as the dependent variable. Data are presented as means ± SEM. There was a main effect of rearing history F(1,202) = 23.47; P = 0.00003, a main effect of testing condition F(1,202) = 158.85; P = 0.00000, and an interaction between rearing history and testing condition F(1,202) = 14.66; P = 0.0002. Post-hoc tests revealed significant differences between peer-reared and mother-reared subjects in the single cage condition, as well as differences between the single cage and social setting conditions within each rearing group (Neuman-Keuls tests, all p < 0.05).

Similar articles

Cited by

References

    1. Adinoff B, Anton R, Linnoila M, Guidotti A, Nemeroff CB, Bissette G. Cerebrospinal fluid concentrations of corticotropin-releasing hormone (CRH) and diazepam-binding inhibitor (DBI) during alcohol withdrawal and abstinence. Neuropsychopharmacology. 1996;15:288–295. - PubMed
    1. Adinoff B, Martin PR, Bone GH, Eckardt MJ, Roehrich L, George DT, Moss HB, Eskay R, Linnoila M, Gold PW. Hypothalamic-pituitary-adrenal axis functioning and cerebrospinal fluid corticotropin releasing hormone and corticotropin levels in alcoholics after recent and long-term abstinence. Arch Gen Psychiatry. 1990;47:325–330. - PubMed
    1. Akil H, Owens C, Gutstein H, Taylor L, Curran E, Watson S. Endogenous opioids: overview and current issues. Drug Alcohol Depend. 1998;51:127–140. - PubMed
    1. Anton RF, Oroszi G, O'Malley S, Couper D, Swift R, Pettinati H, Goldman D. An evaluation of mu-opioid receptor (OPRM1) as a predictor of naltrexone response in the treatment of alcohol dependence: results from the Combined Pharmacotherapies and Behavioral Interventions for Alcohol Dependence (COMBINE) study. Arch Gen Psychiatry. 2008;65:135–144. - PMC - PubMed
    1. Baraona E, Abittan CS, Dohmen K, Moretti M, Pozzato G, Chayes ZW, Schaefer C, Lieber CS. Gender differences in pharmacokinetics of alcohol. Alcohol Clin Exp Res. 2001;25:502–507. - PubMed

MeSH terms