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The brain‐derived neurotrophic factor Val66Met polymorphism affects encoding of object locations during active navigation

The brain‐derived neurotrophic factor (BDNF) was shown to be involved in spatial memory and spatial strategy preference. A naturally occurring single nucleotide polymorphism of the BDNF gene (Val66Met) affects activity‐dependent secretion of BDNF. The current event‐related fMRI study on preselected...

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Autores principales: Wegman, Joost, Tyborowska, Anna, Hoogman, Martine, Arias Vásquez, Alejandro, Janzen, Gabriele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5484279/
https://www.ncbi.nlm.nih.gov/pubmed/27717213
http://dx.doi.org/10.1111/ejn.13416
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author Wegman, Joost
Tyborowska, Anna
Hoogman, Martine
Arias Vásquez, Alejandro
Janzen, Gabriele
author_facet Wegman, Joost
Tyborowska, Anna
Hoogman, Martine
Arias Vásquez, Alejandro
Janzen, Gabriele
author_sort Wegman, Joost
collection PubMed
description The brain‐derived neurotrophic factor (BDNF) was shown to be involved in spatial memory and spatial strategy preference. A naturally occurring single nucleotide polymorphism of the BDNF gene (Val66Met) affects activity‐dependent secretion of BDNF. The current event‐related fMRI study on preselected groups of ‘Met’ carriers and homozygotes of the ‘Val’ allele investigated the role of this polymorphism on encoding and retrieval in a virtual navigation task in 37 healthy volunteers. In each trial, participants navigated toward a target object. During encoding, three positional cues (columns) with directional cues (shadows) were available. During retrieval, the invisible target had to be replaced while either two objects without shadows (objects trial) or one object with a shadow (shadow trial) were available. The experiment consisted of blocks, informing participants of which trial type would be most likely to occur during retrieval. We observed no differences between genetic groups in task performance or time to complete the navigation tasks. The imaging results show that Met carriers compared to Val homozygotes activate the left hippocampus more during successful object location memory encoding. The observed effects were independent of non‐significant performance differences or volumetric differences in the hippocampus. These results indicate that variations of the BDNF gene affect memory encoding during spatial navigation, suggesting that lower levels of BDNF in the hippocampus results in less efficient spatial memory processing.
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spelling pubmed-54842792017-07-10 The brain‐derived neurotrophic factor Val66Met polymorphism affects encoding of object locations during active navigation Wegman, Joost Tyborowska, Anna Hoogman, Martine Arias Vásquez, Alejandro Janzen, Gabriele Eur J Neurosci Cognitive Neuroscience The brain‐derived neurotrophic factor (BDNF) was shown to be involved in spatial memory and spatial strategy preference. A naturally occurring single nucleotide polymorphism of the BDNF gene (Val66Met) affects activity‐dependent secretion of BDNF. The current event‐related fMRI study on preselected groups of ‘Met’ carriers and homozygotes of the ‘Val’ allele investigated the role of this polymorphism on encoding and retrieval in a virtual navigation task in 37 healthy volunteers. In each trial, participants navigated toward a target object. During encoding, three positional cues (columns) with directional cues (shadows) were available. During retrieval, the invisible target had to be replaced while either two objects without shadows (objects trial) or one object with a shadow (shadow trial) were available. The experiment consisted of blocks, informing participants of which trial type would be most likely to occur during retrieval. We observed no differences between genetic groups in task performance or time to complete the navigation tasks. The imaging results show that Met carriers compared to Val homozygotes activate the left hippocampus more during successful object location memory encoding. The observed effects were independent of non‐significant performance differences or volumetric differences in the hippocampus. These results indicate that variations of the BDNF gene affect memory encoding during spatial navigation, suggesting that lower levels of BDNF in the hippocampus results in less efficient spatial memory processing. John Wiley and Sons Inc. 2016-10-14 2017-06 /pmc/articles/PMC5484279/ /pubmed/27717213 http://dx.doi.org/10.1111/ejn.13416 Text en © 2016 The Authors. European Journal of Neuroscience published by Federation of European Neuroscience Societies and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Cognitive Neuroscience
Wegman, Joost
Tyborowska, Anna
Hoogman, Martine
Arias Vásquez, Alejandro
Janzen, Gabriele
The brain‐derived neurotrophic factor Val66Met polymorphism affects encoding of object locations during active navigation
title The brain‐derived neurotrophic factor Val66Met polymorphism affects encoding of object locations during active navigation
title_full The brain‐derived neurotrophic factor Val66Met polymorphism affects encoding of object locations during active navigation
title_fullStr The brain‐derived neurotrophic factor Val66Met polymorphism affects encoding of object locations during active navigation
title_full_unstemmed The brain‐derived neurotrophic factor Val66Met polymorphism affects encoding of object locations during active navigation
title_short The brain‐derived neurotrophic factor Val66Met polymorphism affects encoding of object locations during active navigation
title_sort brain‐derived neurotrophic factor val66met polymorphism affects encoding of object locations during active navigation
topic Cognitive Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5484279/
https://www.ncbi.nlm.nih.gov/pubmed/27717213
http://dx.doi.org/10.1111/ejn.13416
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