Serotonin transporter availability correlates with alcohol intake in non-human primates

A. Heinz, D. W. Jones, J. G. Gorey, A. Bennet, S. J. Suomi, D. R. Weinberger, J. D. Higley

Research output: Contribution to journalArticlepeer-review

Abstract

A low level of alcohol intoxication upon initial exposure and impulsive aggressiveness predispose humans to alcoholism. In non-human primates, central serotonin transporter availability and turnover rate were associated with aggressive behavior and a low response to initial alcohol exposure. We assessed the respective effects of these factors on alcohol intake in a free choice paradigm. Serotonin transporter availability in the raphe area, the origin of central serotonergic projections, was measured with single-photon emission computed tomography and the radioligand [123I]β-CIT in 11 rhesus monkeys with low and high central serotonin turnover. The amount of alcohol intake in the 3-month observation period was positively correlated with serotonin transporter availability (R = 0.76, P = 0.006), but not with aggressiveness (R = 0.19, P = 0.6) or alcohol response upon first exposure (R = -0.48, P = 0.2). In a linear multiple regression analysis with serotonin transporter availability, alcohol response, and aggressiveness as independent variables, 82% of the variance of alcohol intake was explained and serotonin transporter availability emerged as the only statistically significant factor (β = 7.81, P = 0.006). These observations indicate that there may be a direct relationship between serotonin transporter availability and alcohol intake after controlling for aggression and alcohol response on first exposure.

Original languageEnglish (US)
Pages (from-to)231-234
Number of pages4
JournalMolecular psychiatry
Volume8
Issue number2
DOIs
StatePublished - 2003
Externally publishedYes

Keywords

  • Aggressiveness
  • Alcohol response
  • Disposition to alcoholism
  • Molecular neuroimaging
  • β-CIT SPECT

ASJC Scopus subject areas

  • Molecular Biology
  • Psychiatry and Mental health
  • Cellular and Molecular Neuroscience

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