Literature DB >> 33749727

Microscale Physiological Events on the Human Cortical Surface.

Angelique C Paulk1, Jimmy C Yang1,2, Daniel R Cleary3,4,5, Daniel J Soper1, Milan Halgren1,6, Alexandra R O'Donnell1, Sang Heon Lee7, Mehran Ganji7, Yun Goo Ro7, Hongseok Oh7, Lorraine Hossain8, Jihwan Lee7, Youngbin Tchoe7, Nicholas Rogers4, Kivilcim Kiliç3, Sang Baek Ryu2, Seung Woo Lee2, John Hermiz7, Vikash Gilja7, István Ulbert9,10, Daniel Fabó11, Thomas Thesen12,13, Werner K Doyle13, Orrin Devinsky13, Joseph R Madsen14, Donald L Schomer15, Emad N Eskandar2,16, Jong Woo Lee17, Douglas Maus1, Anna Devor3, Shelley I Fried2,18, Pamela S Jones2, Brian V Nahed2, Sharona Ben-Haim5, Sarah K Bick2, Robert Mark Richardson2, Ahmed M Raslan19, Dominic A Siler19, Daniel P Cahill2, Ziv M Williams2, G Rees Cosgrove20, Shadi A Dayeh5,8,21, Sydney S Cash1.   

Abstract

Despite ongoing advances in our understanding of local single-cellular and network-level activity of neuronal populations in the human brain, extraordinarily little is known about their "intermediate" microscale local circuit dynamics. Here, we utilized ultra-high-density microelectrode arrays and a rare opportunity to perform intracranial recordings across multiple cortical areas in human participants to discover three distinct classes of cortical activity that are not locked to ongoing natural brain rhythmic activity. The first included fast waveforms similar to extracellular single-unit activity. The other two types were discrete events with slower waveform dynamics and were found preferentially in upper cortical layers. These second and third types were also observed in rodents, nonhuman primates, and semi-chronic recordings from humans via laminar and Utah array microelectrodes. The rates of all three events were selectively modulated by auditory and electrical stimuli, pharmacological manipulation, and cold saline application and had small causal co-occurrences. These results suggest that the proper combination of high-resolution microelectrodes and analytic techniques can capture neuronal dynamics that lay between somatic action potentials and aggregate population activity. Understanding intermediate microscale dynamics in relation to single-cell and network dynamics may reveal important details about activity in the full cortical circuit.
© The Author(s) 2021. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  auditory stimulation; electrical stimulation; extracellular activity; human cortex; microelectrode

Mesh:

Year:  2021        PMID: 33749727      PMCID: PMC8258438          DOI: 10.1093/cercor/bhab040

Source DB:  PubMed          Journal:  Cereb Cortex        ISSN: 1047-3211            Impact factor:   4.861


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