Literature DB >> 17071238

High-frequency gamma oscillations and human brain mapping with electrocorticography.

Nathan E Crone1, Alon Sinai, Anna Korzeniewska.   

Abstract

Invasive EEG recordings with depth and/or subdural electrodes are occasionally necessary for the surgical management of patients with epilepsy refractory to medications. In addition to their vital clinical utility, electrocorticographic (ECoG) recordings provide an unprecedented opportunity to study the electrophysiological correlates of functional brain activation in greater detail than non-invasive recordings. The proximity of ECoG electrodes to the cortical sources of EEG activity enhances their spatial resolution, as well as their sensitivity and signal-to-noise ratio, particularly for high-frequency EEG activity. ECoG recordings have, therefore, been used to study the event-related dynamics of brain oscillations in a variety of frequency ranges, and in a variety of functional-neuroanatomic systems, including somatosensory and somatomotor systems, visual and auditory perceptual systems, and cortical networks responsible for language. These ECoG studies have confirmed and extended the original non-invasive observations of ERD/ERS phenomena in lower frequencies, and have discovered novel event-related responses in gamma frequencies higher than those previously observed in non-invasive recordings. In particular, broadband event-related gamma responses greater than 60 Hz, extending up to approximately 200 Hz, have been observed in a variety of functional brain systems. The observation of these "high gamma" responses requires a recording system with an adequate sampling rate and dynamic range (we use 1000 Hz at 16-bit A/D resolution) and is facilitated by event-related time-frequency analyses of the recorded signals. The functional response properties of high-gamma activity are distinct from those of ERD/ERS phenomena in lower frequencies. In particular, the timing and spatial localization of high-gamma ERS often appear to be more specific to the putative timing and localization of functional brain activation than alpha or beta ERD/ERS. These findings are consistent with the proposed role of synchronized gamma oscillations in models of neural computation, which have in turn been inspired by observations of gamma activity in animal preparations, albeit at somewhat lower frequencies. Although ECoG recordings cannot directly measure the synchronization of action potentials among assemblies of neurons, they may demonstrate event-related interactions between gamma oscillations in macroscopic local field potentials (LFP) generated by different large-scale populations of neurons engaged by the same functional task. Indeed, preliminary studies suggest that such interactions do occur in gamma frequencies, including high-gamma frequencies, at latencies consistent with the timing of task performance. The neuronal mechanisms underlying high-gamma activity and its unique response properties in humans are still largely unknown, but their investigation through invasive methods is expected to facilitate and expand their potential clinical and research applications, including functional brain mapping, brain-computer interfaces, and neurophysiological studies of human cognition.

Entities:  

Mesh:

Year:  2006        PMID: 17071238     DOI: 10.1016/S0079-6123(06)59019-3

Source DB:  PubMed          Journal:  Prog Brain Res        ISSN: 0079-6123            Impact factor:   2.453


  186 in total

1.  Cortical gamma oscillations modulated by word association tasks: intracranial recording.

Authors:  Lunliya Thampratankul; Tetsuro Nagasawa; Robert Rothermel; Csaba Juhasz; Sandeep Sood; Eishi Asano
Journal:  Epilepsy Behav       Date:  2010-05-06       Impact factor: 2.937

2.  Relationships between spike-free local field potentials and spike timing in human temporal cortex.

Authors:  Stavros Zanos; Theodoros P Zanos; Vasilis Z Marmarelis; George A Ojemann; Eberhard E Fetz
Journal:  J Neurophysiol       Date:  2011-12-07       Impact factor: 2.714

Review 3.  Neurophysiological and computational principles of cortical rhythms in cognition.

Authors:  Xiao-Jing Wang
Journal:  Physiol Rev       Date:  2010-07       Impact factor: 37.312

4.  Intracranial mapping of auditory perception: event-related responses and electrocortical stimulation.

Authors:  A Sinai; N E Crone; H M Wied; P J Franaszczuk; D Miglioretti; D Boatman-Reich
Journal:  Clin Neurophysiol       Date:  2008-12-12       Impact factor: 3.708

5.  Collaborative approach in the development of high-performance brain-computer interfaces for a neuroprosthetic arm: translation from animal models to human control.

Authors:  Jennifer L Collinger; Michael A Kryger; Richard Barbara; Timothy Betler; Kristen Bowsher; Elke H P Brown; Samuel T Clanton; Alan D Degenhart; Stephen T Foldes; Robert A Gaunt; Ferenc E Gyulai; Elizabeth A Harchick; Deborah Harrington; John B Helder; Timothy Hemmes; Matthew S Johannes; Kapil D Katyal; Geoffrey S F Ling; Angus J C McMorland; Karina Palko; Matthew P Para; Janet Scheuermann; Andrew B Schwartz; Elizabeth R Skidmore; Florian Solzbacher; Anita V Srikameswaran; Dennis P Swanson; Scott Swetz; Elizabeth C Tyler-Kabara; Meel Velliste; Wei Wang; Douglas J Weber; Brian Wodlinger; Michael L Boninger
Journal:  Clin Transl Sci       Date:  2013-08-27       Impact factor: 4.689

Review 6.  Interictal high-frequency oscillations in focal human epilepsy.

Authors:  Jan Cimbalnik; Michal T Kucewicz; Greg Worrell
Journal:  Curr Opin Neurol       Date:  2016-04       Impact factor: 5.710

7.  Short-time windowed covariance: a metric for identifying non-stationary, event-related covariant cortical sites.

Authors:  Timothy Blakely; Jeffrey G Ojemann; Rajesh P N Rao
Journal:  J Neurosci Methods       Date:  2013-11-06       Impact factor: 2.390

8.  Gamma activity modulated by naming of ambiguous and unambiguous images: intracranial recording.

Authors:  Yoshimi Cho-Hisamoto; Katsuaki Kojima; Erik C Brown; Naoyuki Matsuzaki; Eishi Asano
Journal:  Clin Neurophysiol       Date:  2014-04-18       Impact factor: 3.708

9.  High γ power in ECoG reflects cortical electrical stimulation effects on unit activity in layers V/VI.

Authors:  Azadeh Yazdan-Shahmorad; Daryl R Kipke; Mark J Lehmkuhle
Journal:  J Neural Eng       Date:  2013-10-08       Impact factor: 5.379

10.  Current Source Mapping by Spontaneous MEG and ECoG in Piglets Model.

Authors:  Lin Gao; Jue Wang; Julia Stephen; Tongsheng Zhang
Journal:  Biomed Signal Process Control       Date:  2015-09-09       Impact factor: 3.880

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.