02594nas a2200325   4500008004100000022001400041245010900055210006900164260001600233300000900249490000700258520156700265653001001832653002301842653002701865653002401892653001301916653001101929653001801940100002101958700001801979700001601997700001902013700002502032700002102057700002302078700001902101700002502120856012302145       2024                        eng d  a2041-172300aMultisensory flicker modulates widespread brain networks and reduces interictal epileptiform discharges.0 aMultisensory flicker modulates widespread brain networks and red  c2024 Apr 11  a31560 v153 a<p>Modulating brain oscillations has strong therapeutic potential. Interventions that both non-invasively modulate deep brain structures and are practical for chronic daily home use are desirable for a variety of therapeutic applications. Repetitive audio-visual stimulation, or sensory flicker, is an accessible approach that modulates hippocampus in mice, but its effects in humans are poorly defined. We therefore quantified the neurophysiological effects of flicker with high spatiotemporal resolution in patients with focal epilepsy who underwent intracranial seizure monitoring. In this interventional trial (NCT04188834) with a cross-over design, subjects underwent different frequencies of flicker stimulation in the same recording session with the effect of sensory flicker exposure on local field potential (LFP) power and interictal epileptiform discharges (IEDs) as primary and secondary outcomes, respectively. Flicker focally modulated local field potentials in expected canonical sensory cortices but also in the medial temporal lobe and prefrontal cortex, likely via resonance of stimulated long-range circuits. Moreover, flicker decreased interictal epileptiform discharges, a pathological biomarker of epilepsy and degenerative diseases, most strongly in regions where potentials were flicker-modulated, especially the visual cortex and medial temporal lobe. This trial met the scientific goal and is now closed. Our findings reveal how multi-sensory stimulation may modulate cortical structures to mitigate pathological activity in humans.</p>10aBrain10aCross-Over Studies10aElectroencephalography10aEpilepsies, Partial10aEpilepsy10aHumans10aTemporal Lobe1 aBlanpain, Lou, T1 aCole, Eric, R1 aChen, Emily1 aPark, James, K1 aWalelign, Michael, Y1 aGross, Robert, E1 aCabaniss, Brian, T1 aWillie, Jon, T1 aSinger, Annabelle, C  uhttps://www.neurotechcenter.org/publications/2024/multisensory-flicker-modulates-widespread-brain-networks-and-reduces01880nas a2200169   4500008004100000022001400041245013300055210006900188260001200257300001200269490000700281520131900288653001801607100001701625700002101642856004701663       1982                        eng d  a0013-469400aScalp distribution of human auditory evoked potentials. II. Evidence for overlapping sources and involvement of auditory cortex.0 aScalp distribution of human auditory evoked potentials II Eviden  c07/1982  a25–380 v543 aThe scalp distributions of human auditory evoked potentials (AEPs) between 20 and 250 msec were investigated using non-cephalic reference recordings. AEPs to binaural click stimuli were recorded simultaneously from 20 scalp locations over the right hemisphere in 11 subjects. Computer-generated isovoltage topographic maps at high temporal resolution were used to assess the stability of AEP scalp distributions over time and relate them to major peaks in the AEP wave forms. For potentials between 20 and 60 msec, the results demonstrate a stable scalp distribution of dipolar form that is consistent with sources in primary auditory cortex on the superior temporal plant near the temporoparietal junction. For potentials between 60 and 250 msec, the results demonstrate changes in AEP morphology across electrode locations and changes in scalp distribution over time that lead to two major conclusions. First, AEPs in this latency period are generated by multiple sources which partially overlap in time. Second, one or more regions of auditory cortex contribute significantly to AEPs in this period. Additional data are needed to determine the relative contribution of auditory cortex sources on the superior temporal plane and the lateral temporal surface and to identify AEP sources outside the temporal lobe.10aTemporal Lobe1 aWood, C., C.1 aWolpaw, Jonathan  uhttp://www.ncbi.nlm.nih.gov/pubmed/6177515