PMID- 25104829 OWN - NLM STAT- MEDLINE DCOM- 20140925 LR - 20211021 IS - 1534-7362 (Electronic) IS - 1534-7362 (Linking) VI - 14 IP - 9 DP - 2014 Aug 7 TI - Paradoxical visuomotor adaptation to reversed visual input is predicted by BDNF Val66Met polymorphism. LID - 10.1167/14.9.4 [doi] LID - 4 AB - Brain-derived neurotrophic factor (BDNF) is the most abundant neurotrophin in the brain, influencing neural development, plasticity, and repair (Chen et al., 2004; Thoenen, 1995). The BDNF gene contains a single-nucleotide polymorphism (SNP) called Val(66)Met. The Met allele interferes with intracellular BDNF-trafficking, decreases activity-dependent BDNF secretion, and consequently is often associated with a shift from plasticity to stability in neural circuits (Egan et al., 2003). We investigated the behavioral consequences of the presence of the Met allele by comparing how 40 heterozygous subjects with the Val/Met genotype and 35 homozygous subjects with the Val/Val genotype performed on visuomotor tasks (reaching and navigation) under two conditions: normal vision and completely left-right reversed vision. As expected, subjects did not differ in their short-term ability to learn the tasks with normal vision (p = 0.58). Intuitively, it would be expected that homozygous Val/Val subjects with a propensity for greater BDNF-induced activity-dependent plasticity would learn new tasks more quickly than heterozygous Val/Met subjects with decreased BDNF secretion (Gilbert, Li, & Piech, 2009). However, we found the opposite here. When short-term mechanisms of visuomotor adaptation were engaged to compensate for the misalignment of visual and somatomotor information created by the left-right reversal of vision, heterozygous Val/Met subjects learned significantly more quickly than their homozygous Val/Val counterparts (p = 0.027). Our results demonstrate the paradoxical finding that the presence of the Met allele, which is thought to promote cortical stability, here improves immediate visuomotor adaptation to left-right-reversed visual input. CI - (c) 2014 ARVO. FAU - Barton, Brian AU - Barton B AD - Department of Cognitive Sciences, University of California, Irvine, CA, USA. FAU - Treister, Andrew AU - Treister A AD - Department of Neurology, University of California, Irvine, CA, USA. FAU - Humphrey, Melanie AU - Humphrey M AD - Department of Cognitive Sciences, University of California, Irvine, CA, USA. FAU - Abedi, Garen AU - Abedi G AD - Department of Neurology, University of California, Irvine, CA, USA. FAU - Cramer, Steven C AU - Cramer SC AD - Departments of Anatomy and Neurobiology and Neurology, University of California, Irvine, CA, USA. FAU - Brewer, Alyssa A AU - Brewer AA AD - Department of Cognitive Sciences, University of California, Irvine, CA, USA. LA - eng GR - K24 HD074722/HD/NICHD NIH HHS/United States GR - L30 EY019249/EY/NEI NIH HHS/United States GR - R01 NS058755/NS/NINDS NIH HHS/United States GR - UL1 TR000153/TR/NCATS NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Research Support, Non-U.S. Gov't DEP - 20140807 PL - United States TA - J Vis JT - Journal of vision JID - 101147197 RN - 0 (Brain-Derived Neurotrophic Factor) RN - 7171WSG8A2 (BDNF protein, human) SB - IM MH - Adaptation, Ocular/*genetics MH - Adolescent MH - Adult MH - Alleles MH - Brain-Derived Neurotrophic Factor/*genetics MH - Chromatography, High Pressure Liquid MH - *Eyeglasses MH - Female MH - Functional Laterality/physiology MH - Genotype MH - Humans MH - Learning/physiology MH - Male MH - Neuronal Plasticity/physiology MH - Pattern Recognition, Visual/*physiology MH - Polymerase Chain Reaction MH - *Polymorphism, Single Nucleotide MH - Psychomotor Performance/*physiology MH - Vision, Binocular/genetics MH - Visual Pathways/physiology MH - Young Adult PMC - PMC4125061 OTO - NOTNLM OT - BDNF OT - plasticity OT - prism adaptation OT - vision OT - visuomotor EDAT- 2014/08/12 06:00 MHDA- 2014/09/26 06:00 PMCR- 2014/08/07 CRDT- 2014/08/09 06:00 PHST- 2014/08/09 06:00 [entrez] PHST- 2014/08/12 06:00 [pubmed] PHST- 2014/09/26 06:00 [medline] PHST- 2014/08/07 00:00 [pmc-release] AID - 14.9.4 [pii] AID - 10.1167/14.9.4 [doi] PST - epublish SO - J Vis. 2014 Aug 7;14(9):4. doi: 10.1167/14.9.4.