Citation

Richter S, Gorny X, Marco-Pallares J, Krämer UM, Machts J, Barman A, Bernstein HG, Schüle R, Schöls L, Rodriguez-Fornells A, Reissner C, Wüstenberg T, Heinze HJ, Gundelfinger ED, Düzel E, Münte TF, Seidenbecher CI, Schott BH. Front. Hum. Neurosci. 2011; 5(online): 175.

Affiliation

Department of Clinical Psychology, University of Salzburg Salzburg, Austria; Leibniz Institute for Neurobiology, Magdeburg, Germany; Helmholtz Center for Neurodegenerative Diseases, Magdeburg, Germany; Department of Physiology II, University of Barcelona and IDIBELL, Barcelona, Spain; Department of Neurology, University of Lübeck, Lübeck, Germany; Institute of Cognitive Neuroscience, University College London, London, UK

Copyright

(Copyright © 2011, Frontiers Research Foundation)

DOI

10.3389/fnhum.2011.00175

PMID

22232585

PMCID

PMC3247758

Abstract

The A-kinase-anchoring protein 5 (AKAP5), a post-synaptic multi-adaptor molecule that binds G-protein-coupled receptors and intracellular signaling molecules has been implicated in emotional processing in rodents, but its role in human emotion and behavior is up to now still not quite clear. Here, we report an association of individual differences in aggressive behavior and anger expression with a functional genetic polymorphism (Pro100Leu) in the human AKAP5 gene. Among a cohort of 527 young, healthy individuals, carriers of the less common Leu allele (15.6% allele frequency) scored significantly lower in the physical aggression domain of the Buss and Perry Aggression Questionnaire and higher in the anger control dimension of the state-trait anger expression inventory. In a functional magnetic resonance imaging experiment we could further demonstrate that AKAP5 Pro100Leu modulates the interaction of negative emotional processing and executive functions. In order to investigate implicit processes of anger control, we used the well-known flanker task to evoke processes of action monitoring and error processing and added task-irrelevant neutral or angry faces in the background of the flanker stimuli. In line with our predictions, Leu carriers showed increased activation of the anterior cingulate cortex (ACC) during emotional interference, which in turn predicted shorter reaction times and might be related to stronger control of emotional interference. Conversely, Pro homozygotes exhibited increased orbitofrontal cortex (OFC) activation during emotional interference, with no behavioral advantage. Immunohistochemistry revealed AKAP5 expression in post mortem human ACC and OFC. Our results suggest that AKAP5 Pro100Leu contributes to individual differences in human aggression and anger control. Further research is warranted to explore the detailed role of AKAP5 and its gene product in human emotion processing.

Language: en