Monoamine oxidase A-uVNTR genotype affects limbic brain activity in response to affective facial stimuli

Byeong Taek Lee, Byung-Joo Ham

Research output: Contribution to journalArticle

48 Citations (Scopus)

Abstract

Monoamine oxidase A (MAOA) enzymatically degrades biogenic amines such as norepinephrine, dopamine, and serotonin, and plays a key role in the regulation of their neurotransmission. Allelic variations at the MAOA locus have been implicated in the neurobiology of aggression and impulsivity. We investigated the possible relationship between the MAOA-upstream variable number of tandem repeats (uVNTR) polymorphism and brain responses to negative facial stimuli, using functional magnetic resonance imaging (fMRI). We found a significant association between a low activity allele of MAOA-uVNTR and neural activation to negative facial stimuli. In the sad condition, participants with the low activity allele showed greater brain activity in the left amygdala. In the angry condition, participants with the low activity allele showed greater brain activity in the right anterior cingulate cortex and hippocampus. Our results suggest that MAOA-uVNTR polymorphism can affect activation of limbic regions, elicited by negative emotional stimuli.

Original languageEnglish
Pages (from-to)515-519
Number of pages5
JournalNeuroReport
Volume19
Issue number5
DOIs
Publication statusPublished - 2008 Mar 1
Externally publishedYes

Fingerprint

Minisatellite Repeats
Monoamine Oxidase
Genotype
Brain
Alleles
Biogenic Amines
Neurobiology
Impulsive Behavior
Gyrus Cinguli
Amygdala
Aggression
Synaptic Transmission
Hippocampus
Dopamine
Serotonin
Norepinephrine
Magnetic Resonance Imaging

Keywords

  • Anger
  • Functional magnetic resonance imaging
  • Monoamine oxidase A
  • Polymorphism
  • Sadness

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

Monoamine oxidase A-uVNTR genotype affects limbic brain activity in response to affective facial stimuli. / Lee, Byeong Taek; Ham, Byung-Joo.

In: NeuroReport, Vol. 19, No. 5, 01.03.2008, p. 515-519.

Research output: Contribution to journalArticle

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