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1.
PeerJ ; 6: e4906, 2018.
Article in English | MEDLINE | ID: mdl-29868292

ABSTRACT

BACKGROUND: Working memory, as a complex system, consists of two independent components: manipulation and maintenance process, which are defined as executive control and storage process. Previous studies mainly focused on the overall effect of transcranial direct current stimulation (tDCS) on working memory. However, little has been known about the segregative effects of tDCS on the sub-processes within working memory. METHOD: Transcranial direct current stimulation, as one of the non-invasive brain stimulation techniques, is being widely used to modulate the cortical activation of local brain areas. This study modified a spatial n-back experiment with anodal and cathodal tDCS exertion on the right dorsolateral prefrontal cortex (DLPFC), aiming to investigate the effects of tDCS on the two sub-processes of working memory: manipulation (updating) and maintenance. Meanwhile, considering the separability of tDCS effects, we further reconfirmed the causal relationship between the right DLPFC and the sub-processes of working memory with different tDCS conditions. RESULTS: The present study showed that cathodal tDCS on the right DLPFC selectively improved the performance of the modified 2-back task in the difficult condition, whereas anodal tDCS significantly reduced the performance of subjects and showed an speeding-up tendency of response time. More precisely, the results of discriminability index and criterion showed that only cathodal tDCS enhanced the performance of maintenance in the difficult condition. Neither of the two tDCS conditions affected the performance of manipulation (updating). CONCLUSION: These findings provide evidence that cathodal tDCS of the right DLPFC selectively affects maintenance capacity. Besides, cathodal tDCS also serves as an interference suppressor to reduce the irrelevant interference, thereby indirectly improving the working memory capacity. Moreover, the right DLPFC is not the unique brain regions for working memory manipulation (updating).

2.
J Exp Psychol Hum Percept Perform ; 44(5): 767-777, 2018 May.
Article in English | MEDLINE | ID: mdl-29154628

ABSTRACT

Our previous work suggests that 2 colors can be consolidated into visual short-term memory (VSTM) in parallel without a loss of memory precision, whereas consolidation of 2 orientations is performed in a strictly serial manner. Those experiments compared VSTM performance for simultaneously and sequentially presented stimuli. However, there is still controversy about whether the bandwidth for consolidation is determined by the type of information. To further investigate this issue, here we measured electroencephalography while participants attempted to consolidate 1, 2 or 4 simultaneously presented colors (Experiment 1) or orientations (Experiment 2) under limited presentation times. We used the contralateral delay activity (CDA) as an electrophysiological marker of the number of items that were consolidated. For colored stimuli, the CDA amplitude increased between set-size 1 and 2 but did not further increase for set size 4. By contrast, for orientation, the CDA amplitude remained at the set size 1 amplitude as set size increased to 2 or 4 items. Furthermore, in a long exposure duration (300 ms) condition that did not limit the consolidation process, the CDA amplitude pattern indicated that VSTM capacity is limited to about 3 colored items and about 2 orientation items in our paradigm. Thus, the CDA effects observed in the short presentation time was not limited by VSTM storage, but rather by consolidation. These results are consistent with our previous behavioral research and suggest that the bandwidth of VSTM consolidation is determined by the stimulus feature. (PsycINFO Database Record


Subject(s)
Cerebral Cortex/physiology , Evoked Potentials/physiology , Memory Consolidation/physiology , Memory, Short-Term/physiology , Psychomotor Performance/physiology , Visual Perception/physiology , Adult , Arabidopsis Proteins , Electroencephalography , Female , Humans , Male , Nuclear Proteins , Young Adult
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