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109. Photosensitive epilepsy: Role of corpus callosum in cortical excitability
- Source :
- Clinical Neurophysiology. 126:e25
- Publication Year :
- 2015
- Publisher :
- Elsevier BV, 2015.
-
Abstract
- Photosensitive epilepsy (PE) is a form of epileptic seizure induced by several powerful visual stimuli. Cortical mechanisms underlying paroxysmal activity have been widely studied in several ways. Here, we employed rTMS in an attempt to disclose the role of callosal input in modulating cortical visual excitability in both healthy subjects and PE patients. We enrolled 10 healthy subjects (5 males and 5 females; mean age 16.8 ± 3.4 yrs) and 5 patients (15.9 ± 4.2 yrs). Visual evoked potentials (VEPs) triggered by grating stimuli of different contrasts were recorded before and after functional inactivation of the occipital cortex of one hemisphere via off-line low-frequency repetitive transcranial magnetic stimulation (rTMS; 0.5 Hz stimulation for 20 min). VEPs were recorded in V1 before (T0), immediately after (T1) and 45′ following the end of rTMS (T2). We found that low-frequency rTMS had an inhibitory effect on VEP amplitudes at all contrasts in the treated side in controls and patients. Reduction of VEP amplitudes in the inhibited hemisphere at T1 was accompanied by an increase in VEP amplitudes in the contralateral side at mid-high contrasts (50–90%) in healthy subjects ( p p p
- Subjects :
- Visual perception
genetic structures
musculoskeletal, neural, and ocular physiology
medicine.medical_treatment
Stimulation
Visual evoked potentials
Corpus callosum
medicine.disease
Sensory Systems
Transcranial magnetic stimulation
medicine.anatomical_structure
Neurology
Photosensitive epilepsy
Physiology (medical)
Cortex (anatomy)
medicine
Neurology (clinical)
Epileptic seizure
medicine.symptom
Psychology
Neuroscience
Subjects
Details
- ISSN :
- 13882457
- Volume :
- 126
- Database :
- OpenAIRE
- Journal :
- Clinical Neurophysiology
- Accession number :
- edsair.doi...........f59b954b04e73344bcf44a68bf20afa2
- Full Text :
- https://doi.org/10.1016/j.clinph.2014.10.128