Repetitive Paired-Pulse Transcranial Magnetic Stimulation Over the Visual Cortex Alters Visual Recovery Function

2013 ◽  
Vol 6 (3) ◽  
pp. 298-305 ◽  
Author(s):  
Takahiro Kimura ◽  
Katsuya Ogata ◽  
Shozo Tobimatsu
2020 ◽  
Vol 131 (4) ◽  
pp. e76
Author(s):  
D. Khammash ◽  
M. Simmonite ◽  
T.A. Polk ◽  
S.F. Taylor ◽  
S.K. Meehan

2005 ◽  
Vol 382 (3) ◽  
pp. 312-316 ◽  
Author(s):  
Roland Sparing ◽  
Nina Dambeck ◽  
Kathrin Stock ◽  
Ingo G. Meister ◽  
Dorothee Huetter ◽  
...  

2020 ◽  
Vol 730 ◽  
pp. 135022 ◽  
Author(s):  
Olga Lucia Gamboa ◽  
Alexandra Brito ◽  
Zachary Abzug ◽  
Tracy D’Arbeloff ◽  
Lysianne Beynel ◽  
...  

2019 ◽  
Author(s):  
Olga Lucia Gamboa Arana ◽  
Alexandra Brito ◽  
Zachary Abzug ◽  
Tracy D’Arbeloff ◽  
Lysianne Beynel ◽  
...  

ABSTRACTThe perception of visual motion is dependent on a set of occipitotemporal regions which are readily accessible to neuromodulation. Previous studies using paired-pulse Transcranial Magnetic Stimulation (ppTMS) have provided evidence of the capacity of this type of protocols to modulate cognitive processes. To test whether such cortical modulation can be observed in the visual system, particularly during motion perception, ppTMS was applied to the occipital cortex using both scalp-based and meta-analytic targeting coordinates. In this within-subject, sham-controlled study, fifteen subjects completed two sessions in two consecutive weeks. On the first visit, subject-specific resting motor threshold (RMT) was determined and participants performed an adaptive motion discrimination task to determine individual motion sensitivity. During the second visit, subjects performed the same task with three individualized difficulty levels as two TMS pulses were delivered respectively −150 and −50 ms prior to motion stimulus onset at 120% RMT, under the logic that the cumulative inhibitory effect of these two pulses would alter motion sensitivity as measured by the individually calibrated task. The ppTMS was delivered at one of two locations: 3 cm dorsal and 5 cm lateral to inion (scalp-based coordinate), or at the site of peak activation for “motion” according to the NeuroSynth fMRI database (meta-analytic coordinate). Sham stimulation was delivered on one-third of trials and evenly between the two targets. Analyses showed no significant active-versus-sham effects of ppTMS when stimulation was delivered to the meta-analytic (p = 0.15) or scalp-based coordinates (p = 0.17), which were separated by 29 mm on average. Additionally, there was no was significant interaction between ppTMS at either location and task difficulty level (p = 0.12 and p = 0.33, respectively). These findings fail to support the hypothesis that long-interval ppTMS recruits inhibitory processes in motion-sensitive cortex, but must be considered within the limits of the current design choices.HIGHLIGHTSLong-interval paired-pulse TMS was applied to visual cortex during a motion taskThe ppTMS was delivered according to scalp and meta-analytic coordinates, as well as shamNo effects of active-versus-sham stimulation were observed on motion task performance


2014 ◽  
Vol 7 (2) ◽  
pp. 275-280 ◽  
Author(s):  
Takahiro Kimura ◽  
Katsuya Ogata ◽  
Hisato Nakazono ◽  
Shozo Tobimatsu

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Domenica Veniero ◽  
Joachim Gross ◽  
Stephanie Morand ◽  
Felix Duecker ◽  
Alexander T. Sack ◽  
...  

AbstractVoluntary allocation of visual attention is controlled by top-down signals generated within the Frontal Eye Fields (FEFs) that can change the excitability of lower-level visual areas. However, the mechanism through which this control is achieved remains elusive. Here, we emulated the generation of an attentional signal using single-pulse transcranial magnetic stimulation to activate the FEFs and tracked its consequences over the visual cortex. First, we documented changes to brain oscillations using electroencephalography and found evidence for a phase reset over occipital sites at beta frequency. We then probed for perceptual consequences of this top-down triggered phase reset and assessed its anatomical specificity. We show that FEF activation leads to cyclic modulation of visual perception and extrastriate but not primary visual cortex excitability, again at beta frequency. We conclude that top-down signals originating in FEF causally shape visual cortex activity and perception through mechanisms of oscillatory realignment.


2002 ◽  
Vol 333 (2) ◽  
pp. 83-86 ◽  
Author(s):  
Andon R Kossev ◽  
Christoph Schrader ◽  
Jan Däuper ◽  
Reinhard Dengler ◽  
Jens D Rollnik

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