Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/65999
Citations
Scopus Web of Science® Altmetric
?
?
Type: Journal article
Title: Paradoxical association of the brain-derived-neurotrophic-factor val66met genotype with response inhibition
Author: Beste, C.
Baune, B.
Domschke, K.
Falkenstein, M.
Konrad, C.
Citation: Neuroscience, 2010; 166(1):178-184
Publisher: Pergamon-Elsevier Science Ltd
Issue Date: 2010
ISSN: 0306-4522
1873-7544
Statement of
Responsibility: 
C. Beste, B. T. Baune, K. Domschke, M. Falkenstein and C. Konrad
Abstract: Response inhibition is a basic executive function which is dysfunctional in various basal ganglia diseases. The brain-derived-neurotrophic-factor (BDNF) plays an important pathophysiological role in these diseases. In the current study we examined the functional relevance of the BDNF val66met polymorphism for response inhibition processes in 57 healthy human subjects using event-related potentials (ERPs), i.e. the Nogo-N2 and Nogo-P3, which likely reflect different aspects of inhibition. Our results support the pre-motor inhibition theory of the Nogo-N2. We show that the BDNF val66met polymorphism selectively modulates the Nogo-N2. Response inhibition was better in the val/met-met/met group, since this group committed fewer false alarms, and their Nogo-N2 was larger, compared to the val/val group. This is the first study showing that met alleles of the BDNF val66met polymorphism confer an advantage for a specific cognitive function. We propose a neuronal model how this advantage gets manifest on a neuronal level.
Keywords: response inhibition
event-related potentials (ERPs)
Nogo-N2
Nogo-P3
basal ganglia
BDNF val66met
Rights: © 2010 IBRO
DOI: 10.1016/j.neuroscience.2009.12.022
Published version: http://dx.doi.org/10.1016/j.neuroscience.2009.12.022
Appears in Collections:Aurora harvest
Psychiatry publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.