4.5 Article

Central nervous system serotonergic responsivity and aggressive disposition in men

Journal

PHYSIOLOGY & BEHAVIOR
Volume 77, Issue 4-5, Pages 705-709

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0031-9384(02)00922-8

Keywords

aggression; serotonin; fenfluramine challenge; genetics; monoamine-oxidase A

Funding

  1. NHLBI NIH HHS [HL-65137, HL-40962, HL-46328] Funding Source: Medline

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To determine whether normative variability in aggressive behavior correlates negatively with central nervous system (CNS) serotonergic function among men, plasma prolactin (PRL) responses to a standard fenfluramine challenge (administered to assess central serotonergic responsivity) were examined in relation to interview-assessed aggression histories among 118 adult males derived from a nonpatient, community sample. Fenfluramine-induced, peak PRL rises were smaller in subjects whose 'aggression' scores fell above the sample median, compared to their less aggressive counterparts (P<.002). Across subjects, participants' peak PRL responses likewise covaried inversely with aggression history (r(s) = -.32, P <.0005). Additional analyses were conducted on data of 58 subjects who had also been genotyped for a functional polymorphism in the promoter region of the X chromosomal, monoamine oxidase-A (MAO-A) gene. The four variants of this repeat polymorphism were grouped for analysis (alleles '1 + 4' vs. '2 + 3') based on prior report of enhanced transcriptional efficiency in MAO-A promoter constructs containing alleles 2 and 3 (repeats of intermediate length). Men in the 2/3 allele group had significantly higher aggression scores (P <.05) and smaller peak PRL responses to fenfluramine (P <.009) than men in the 1/4 allele group. When adjusted by analysis of covariance for concomitant variability in subjects' PRL responses, aggressive disposition no longer varied significantly by genotype. This finding suggests that association of the MAO-A promoter polymorphism with this behavioral phenotype may be mediated, in part, by allele-specific variation in central serotonergic responsivity. (C) 2002 Elsevier Science Inc. All rights reserved.

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