1.
Posttraining transcranial magnetic stimulation of striate cortex disrupts consolidation early in visual skill learning.
De Weerd, P, Reithler, J, van de Ven, V, Been, M, Jacobs, C, Sack, AT
The Journal of neuroscience : the official journal of the Society for Neuroscience. 2012;(6):1981-8
Abstract
Practice-induced improvements in skilled performance reflect "offline " consolidation processes extending beyond daily training sessions. According to visual learning theories, an early, fast learning phase driven by high-level areas is followed by a late, asymptotic learning phase driven by low-level, retinotopic areas when higher resolution is required. Thus, low-level areas would not contribute to learning and offline consolidation until late learning. Recent studies have challenged this notion, demonstrating modified responses to trained stimuli in primary visual cortex (V1) and offline activity after very limited training. However, the behavioral relevance of modified V1 activity for offline consolidation of visual skill memory in V1 after early training sessions remains unclear. Here, we used neuronavigated transcranial magnetic stimulation (TMS) directed to a trained retinotopic V1 location to test for behaviorally relevant consolidation in human low-level visual cortex. Applying TMS to the trained V1 location within 45 min of the first or second training session strongly interfered with learning, as measured by impaired performance the next day. The interference was conditional on task context and occurred only when training in the location targeted by TMS was followed by training in a second location before TMS. In this condition, high-level areas may become coupled to the second location and uncoupled from the previously trained low-level representation, thereby rendering consolidation vulnerable to interference. Our data show that, during the earliest phases of skill learning in the lowest-level visual areas, a behaviorally relevant form of consolidation exists of which the robustness is controlled by high-level, contextual factors.
2.
The functional BDNF Val66Met polymorphism affects functions of pre-attentive visual sensory memory processes.
Beste, C, Schneider, D, Epplen, JT, Arning, L
Neuropharmacology. 2011;(2-3):467-71
Abstract
The brain-derived neurotrophic factor (BDNF), a member of the neurotrophin family, is involved in nerve growth and survival. Especially, a single nucleotide polymorphism (SNP) in the BDNF gene, Val66Met, has gained a lot of attention, because of its effect on activity-dependent BDNF secretion and its link to impaired memory processes. We hypothesize that the BDNF Val66Met polymorphism may have modulatory effects on the visual sensory (iconic) memory performance. Two hundred and eleven healthy German students (106 female and 105 male) were included in the data analysis. Since BDNF is also discussed to be involved in the pathogenesis of depression, we additionally tested for possible interactions with depressive mood. The BDNF Val66Met polymorphism significantly influenced iconic-memory performance, with the combined Val/Met-Met/Met genotype group revealing less time stability of information stored in iconic memory than the Val/Val group. Furthermore, this stability was positively correlated with depressive mood exclusively in the Val/Val genotype group. Thus, these results show that the BDNF Val66Met polymorphism has an effect on pre-attentive visual sensory memory processes.
3.
Effects of pharmacologically induced changes in NMDA receptor activity on human timing and sensorimotor performance.
Rammsayer, TH
Brain research. 2006;:407-16
Abstract
Unlike processing of time intervals in the range of seconds or more, processing of brief durations in the subsecond range appears to be beyond cognitive control and based on subcortical mechanisms located in the basal ganglia. The present study was designed to evaluate the effects of NMDA receptor activity on temporal processing in the second and subsecond range. In a double-blind crossover design, either 30 mg of the noncompetitive NMDA receptor antagonist memantine or placebo was administered to 32 healthy male volunteers. While memantine induced a marked impairment in temporal processing of intervals in the range of seconds, temporal processing of intervals in the range of milliseconds was not affected. Furthermore, no effect of memantine on speed of information processing could be observed. Speed of motor response execution, however, was significantly enhanced by memantine compared to placebo. The overall pattern of results provides converging evidence for the notion that temporal processing of longer intervals involves higher order working memory functions such as working memory capacity. The absence of an effect on temporal processing of very brief intervals in combination with the beneficial effect on movement time suggests that NMDA receptor activity in the basal ganglia is not directly related to the timing of intervals in the subsecond range.