A multimodal perspective on the composition of cortical oscillations

• Published in: Frontiers in human neuroscience 2013, Vol.7, p.132-132
• Main Authors: Ronnqvist, Kim C, McAllister, Craig J, Woodhall, Gavin L, Stanford, Ian M, Hall, Stephen D
• Format: Article
• Language: English
• Subjects: Beta Rhythm; Brain; connectivity; Consanguinity; Cortex (motor); EEG; Experiments; Functional magnetic resonance imaging; GABA; Magnetoencephalography; Neural networks; Neuroimaging; Neuroscience; Neurosciences; NMR; Nuclear magnetic resonance; Oscillations; Researchers; Rhythm; Signal processing; Signatures; stimulation; Studies; Zolpidem; γ-Aminobutyric acid
• ISSN: 1662-5161; 1662-5161
• DOI: 10.3389/fnhum.2013.00132

An expanding corpus of research details the relationship between functional magnetic resonance imaging (fMRI) measures and neuronal network oscillations. Typically, integrated electroencephalography and fMRI, or parallel magnetoencephalography (MEG) and fMRI are used to draw inference about the consanguinity of BOLD and electrical measurements. However, there is a relative dearth of information about the relationship between E/MEG and the focal networks from which these signals emanate. Consequently, the genesis and composition of E/MEG oscillations requires further clarification. Here we aim to contribute to understanding through a series of parallel measurements of primary motor cortex (M1) oscillations, using human MEG and in vitro rodent local field potentials. We compare spontaneous activity in the ∼10 Hz mu and 15-30 Hz beta frequency ranges and compare MEG signals with independent and integrated layers III and V (LIII/LV) from in vitro recordings. We explore the mechanisms of oscillatory generation, using specific pharmacological modulation with the GABA-A alpha-1 subunit modulator zolpidem. Finally, to determine the contribution of cortico-cortical connectivity, we recorded in vitro M1, during an incision to sever lateral connections between M1 and S1 cortices. We demonstrate that frequency distribution of MEG signals appear have closer statistically similarity with signals from integrated rather than independent LIII/LV laminae. GABAergic modulation in both modalities elicited comparable changes in the power of the beta band. Finally, cortico-cortical connectivity in sensorimotor cortex (SMC) appears to directly influence the power of the mu rhythm in LIII. These findings suggest that the MEG signal is an amalgam of outputs from LIII and LV, that multiple frequencies can arise from the same cortical area and that in vitro and MEG M1 oscillations are driven by comparable mechanisms. Finally, cortico-cortical connectivity is reflected in the power of the SMC mu rhythm.