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High trait aggression in men is associated with low 5-HT levels, as indexed by 5-HT4 receptor binding.

Authors :
da Cunha-Bang S
Mc Mahon B
Fisher PM
Jensen PS
Svarer C
Knudsen GM
Source :
Social cognitive and affective neuroscience [Soc Cogn Affect Neurosci] 2016 Apr; Vol. 11 (4), pp. 548-55. Date of Electronic Publication: 2016 Jan 15.
Publication Year :
2016

Abstract

Impulsive aggression has commonly been associated with a dysfunction of the serotonin (5-HT) system: many, but not all, studies point to an inverse relationship between 5-HT and aggression. As cerebral 5-HT4 receptor (5-HT4R) binding has recently been recognized as a proxy for stable brain levels of 5-HT, we here test the hypothesis in healthy men and women that brain 5-HT levels, as indexed by cerebral 5-HT4R, are inversely correlated with trait aggression and impulsivity. Sixty-one individuals (47 men) underwent positron emission tomography scanning with the radioligand [(11)C]SB207145 for quantification of brain 5-HT4R binding. The Buss-Perry Aggression Questionnaire (BPAQ) and the Barratt Impulsiveness Scale were used for assessment of trait aggression and trait impulsivity. Among male subjects, there was a positive correlation between global 5-HT4R and BPAQ total score (Pā€‰=ā€‰0.037) as well as BPAQ physical aggression (Pā€‰=ā€‰0.025). No main effect of global 5-HT4R on trait aggression or impulsivity was found in the mixed gender sample, but there was evidence for sex interaction effects in the relationship between global 5-HT4R and BPAQ physical aggression. In conclusion we found that low cerebral 5-HT levels, as indexed by 5-HT4R binding were associated with high trait aggression in males, but not in females.<br /> (© The Author (2016). Published by Oxford University Press. For Permissions, please email: journals.permissions@oup.com.)

Details

Language :
English
ISSN :
1749-5024
Volume :
11
Issue :
4
Database :
MEDLINE
Journal :
Social cognitive and affective neuroscience
Publication Type :
Academic Journal
Accession number :
26772668
Full Text :
https://doi.org/10.1093/scan/nsv140