Volume 42, Issue 2 pp. 424-431
Original Article

Low Inherent Sensitivity to the Intoxicating Effects of Ethanol in Rhesus Monkeys with Low CSF Concentrations of the Serotonin Metabolite 5-Hydroxyindoleacetic Acid

Elizabeth K. Wood

Elizabeth K. Wood

Department of Psychology, Brigham Young University, Provo, Utah

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Ryno Kruger

Ryno Kruger

Department of Psychology, Brigham Young University, Provo, Utah

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Angus Bennion

Angus Bennion

Department of Psychology, Brigham Young University, Provo, Utah

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Bradley M. Cooke

Bradley M. Cooke

Georgia State University, Atlanta, Georgia

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Stephen Lindell

Stephen Lindell

Laboratory of Clinical Studies, DICBR, NIAAA, Bethesda, Maryland

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Melanie Schwandt

Melanie Schwandt

Laboratory of Clinical Studies, DICBR, NIAAA, Bethesda, Maryland

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David Goldman

David Goldman

Laboratory of Neurogenetics, National Institute on Alcohol Abuse and Alcoholism, Rockville, Maryland

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Christina S. Barr

Christina S. Barr

Laboratory of Clinical Studies, DICBR, NIAAA, Bethesda, Maryland

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Stephen J. Suomi

Stephen J. Suomi

Laboratory of Comparative Ethology, NICHD, NIH Animal Center, Poolesville, Maryland

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James Dee Higley

Corresponding Author

James Dee Higley

Department of Psychology, Brigham Young University, Provo, Utah

Reprint requests: James Dee Higley, Department of Psychology, Brigham Young University, 1042 SWKT, Provo, UT 84602; Tel: 801-851-0845 Fax: 801-422-0602; E-mail: [email protected]Search for more papers by this author
First published: 10 November 2017
Citations: 4

Abstract

Background

Type 2 alcoholism is characterized by low serotonin system functioning and has a high degree of heritability, with offspring of alcoholics often showing a reduced response to the intoxicating effects of ethanol (EtOH), which is thought to be marker for future alcohol use disorders (AUDs). As such, an important aim of studies investigating the origins of AUDs is to understand the relationship between serotonin system functioning and level of intoxication. A nonhuman primate model was used to evaluate observational ratings of sensitivity to EtOH and to further investigate the relationship between central serotonin activity and behavioral response to EtOH.

Methods

Cerebrospinal fluid (CSF) concentrations of 5-hydroxyindoleacetic acid (5-HIAA) were obtained from 4 cohorts of alcohol-naïve, adolescent rhesus macaques (N = 82, 45 females, 37 males). One to 3 months after the CSF sample, subjects were administered a standardized intravenous EtOH bolus (males: 2.1 g/kg body weight, females: 2.0 g/kg body weight), placed into an open-top, clear plexiglass chamber suspended from the ceiling, and their latency to escape was recorded as a measure of the degree of intoxication. Thereafter, subjects were rated using a Likert scale for the degree of intoxication during a 30-minute observation period.

Results

Our results indicate that latency to escape from the chamber was associated with intoxication ratings (= 0.0009) following the standardized intravenous administration of EtOH. Low CSF 5-HIAA concentrations predicted short escape latency (= 0.007) and were associated with low intoxication ratings (= 0.02), indicating that low central nervous system (CNS) serotonin functioning is related to relative insensitivity to the intoxicating effects of alcohol.

Conclusions

Our study shows that, in monkeys exposed to alcohol for the first time, objective measures of intoxication are associated with subjective ratings for intoxication, and both were associated with CSF 5-HIAA concentrations. Our data confirm and extend the finding that low CNS serotonin functioning is predictive of intrinsic low sensitivity to the intoxicating effects of EtOH.

Graphical Abstract

Cisternal CSF concentrations of the serotonin metabolite 5-HIAA were obtained from adolescent alcohol-naïve rhesus monkeys. Shortly after, they were infused with an intravenous dose of ethanol (EtOH) and rated for intoxication. Subjects rated as low in intoxication exhibited low CSF 5-HIAA concentrations. This finding suggests an association between impaired central serotonin functioning and relative insensitivity to EtOH, and that impaired central serotonin functioning may lead to a low level of response to alcohol, both of which are characteristics of Type 2 alcoholism.

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