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Co-occurring ripple oscillations facilitate neuronal interactions between cortical locations in humans.
Verzhbinsky, Ilya A; Rubin, Daniel B; Kajfez, Sophie; Bu, Yiting; Kelemen, Jessica N; Kapitonava, Anastasia; Williams, Ziv M; Hochberg, Leigh R; Cash, Sydney S; Halgren, Eric.
Afiliação
  • Verzhbinsky IA; Neurosciences Graduate Program, University of California San Diego, La Jolla, CA 92093.
  • Rubin DB; Medical Scientist Training Program, University of California San Diego, La Jolla, CA 92093.
  • Kajfez S; Department of Neurology, Center for Neurotechnology and Neurorecovery, Massachusetts General Hospital, Boston, MA 02114.
  • Bu Y; Department of Radiology, University of California San Diego, La Jolla, CA 92093.
  • Kelemen JN; Department of Neurosciences, University of California San Diego, La Jolla, CA 92093.
  • Kapitonava A; Department of Neurology, Center for Neurotechnology and Neurorecovery, Massachusetts General Hospital, Boston, MA 02114.
  • Williams ZM; Department of Neurology, Center for Neurotechnology and Neurorecovery, Massachusetts General Hospital, Boston, MA 02114.
  • Hochberg LR; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA 02114.
  • Cash SS; Department of Neurology, Center for Neurotechnology and Neurorecovery, Massachusetts General Hospital, Boston, MA 02114.
  • Halgren E; Center for Neurorestoration and Neurotechnology, Department of Veterans Affairs, Providence, RI 02908.
Proc Natl Acad Sci U S A ; 121(1): e2312204121, 2024 Jan 02.
Article em En | MEDLINE | ID: mdl-38157452
ABSTRACT
How the human cortex integrates ("binds") information encoded by spatially distributed neurons remains largely unknown. One hypothesis suggests that synchronous bursts of high-frequency oscillations ("ripples") contribute to binding by facilitating integration of neuronal firing across different cortical locations. While studies have demonstrated that ripples modulate local activity in the cortex, it is not known whether their co-occurrence coordinates neural firing across larger distances. We tested this hypothesis using local field-potentials and single-unit firing from four 96-channel microelectrode arrays in the supragranular cortex of 3 patients. Neurons in co-rippling locations showed increased short-latency co-firing, prediction of each other's firing, and co-participation in neural assemblies. Effects were similar for putative pyramidal and interneurons, during non-rapid eye movement sleep and waking, in temporal and Rolandic cortices, and at distances up to 16 mm (the longest tested). Increased co-prediction during co-ripples was maintained when firing-rate changes were equated, indicating that it was not secondary to non-oscillatory activation. Co-rippling enhanced prediction was strongly modulated by ripple phase, supporting the most common posited mechanism for binding-by-synchrony. Co-ripple enhanced prediction is reciprocal, synergistic with local upstates, and further enhanced when multiple sites co-ripple, supporting re-entrant facilitation. Together, these results support the hypothesis that trans-cortical co-occurring ripples increase the integration of neuronal firing of neurons in different cortical locations and do so in part through phase-modulation rather than unstructured activation.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Interneurônios / Neurônios Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Interneurônios / Neurônios Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article