TY - JOUR PY - 1998// TI - In vivo association between alcohol intoxication, aggression, and serotonin transporter availability in nonhuman primates JO - American journal of psychiatry A1 - Heinz, A. A1 - Higley, J. D. A1 - Gorey, J. G. A1 - Saunders, R. C. A1 - Jones, D. W. A1 - Hommer, D. A1 - Zajicek, K. A1 - Suomi, S. J. A1 - Lesch, K. P. A1 - Weinberger, D. R. A1 - Linnoila, M. SP - 1023 EP - 1028 VL - 155 IS - 8 N2 - OBJECTIVE: Studies on brain serotonin metabolism in human and nonhuman primates have indicated that dysfunction of serotonin transmission may play a role in the biological vulnerability to dependence on alcohol. Among young men, low sensitivity to alcohol intoxication predicts subsequent alcohol abuse and dependence. METHOD: The authors used single photon emission computed tomography and the radioligand [(I)123]beta-CIT ([(I)123]methyl 3beta-(4-iodophenyl) tropane-2-carboxylate) to measure the availability of serotonin transporters in 11 male rhesus monkeys, and the monkeys were genotyped for a functional polymorphism of the serotonin transporter gene. The 11 monkeys had experienced parental separation after birth; their behavior and 5-hydroxyindoleacetic acid (5-HIAA) concentrations in CSF had been assessed regularly. RESULTS: In the 5-year-old monkeys, there was a significant negative correlation between beta-CIT binding to serotonin transporters in the brainstem and 5-HIAA concentrations in CSF. Animals with greater beta-CIT binding and low CSF 5-HIAA concentrations displayed greater aggressiveness and were less sensitive to alcohol-induced intoxication. The genetic constitution of the serotonin transporter promoter gene did not significantly contribute to the availability of brainstem serotonin transporters as measured by beta-CIT binding. CONCLUSIONS: In adult nonhuman primates who underwent early developmental stress, variables indicating a low serotonin turnover rate were associated with behavior patterns similar to those predisposing to early-onset alcoholism among humans.
Language: en
LA - en SN - 0002-953X UR - http://dx.doi.org/ ID - ref1 ER -