Noninvasive measurement of dynamic brain signals using light penetrating the brain

Conventional techniques for the noninvasive measurement of brain activity involve critical limitations in spatial or temporal resolution. Here, we propose the method for noninvasive brain function measurement with high spatiotemporal resolution using optical signals. We verified that diffused near-infrared light penetrating through the upper jaw and into the skull, which we term as optoencephalography (OEG), leads to the detection of dynamic brain signals that vary concurrently with the electrophysiological neural activity. We measured the OEG signals following the stimulation of the median nerve in common marmosets. The OEG signal response was tightly coupled with the electrophysiological response represented by the somatosensory evoked potential (SSEP). The OEG measurement is also shown to offer rather clear discrimination of brain signals.

[1]  T. Allison,et al.  Distribution of cerebral somatosensory evoked responses in normal man , 1962 .

[2]  R. Keynes,et al.  Light Scattering and Birefringence Changes during Nerve Activity , 1968, Nature.

[3]  D. Kleinfeld,et al.  Noninvasive detection of changes in membrane potential in cultured neurons by light scattering. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[4]  A. Villringer,et al.  Near infrared spectroscopy (NIRS): A new tool to study hemodynamic changes during activation of brain function in human adults , 1993, Neuroscience Letters.

[5]  D. Hood,et al.  Shades of gray matter: noninvasive optical images of human brain responses during visual stimulation. , 1995, Psychophysiology.

[6]  B. Chance,et al.  Photon migration in the presence of a single defect: a perturbation analysis. , 1995, Applied optics.

[7]  D. Hood,et al.  Fast and Localized Event-Related Optical Signals (EROS) in the Human Occipital Cortex: Comparisons with the Visual Evoked Potential and fMRI , 1997, NeuroImage.

[8]  F. Varela,et al.  Measuring phase synchrony in brain signals , 1999, Human brain mapping.

[9]  Olivier David,et al.  Estimation of neural dynamics from MEG/EEG cortical current density maps: application to the reconstruction of large-scale cortical synchrony , 2002, IEEE Transactions on Biomedical Engineering.

[10]  Hellmuth Obrig,et al.  The fast optical signal—Robust or elusive when non-invasively measured in the human adult? , 2005, NeuroImage.

[11]  Benjamin Barrowes,et al.  Cross-polarized reflected light measurement of fast optical responses associated with neural activation. , 2005, Biophysical journal.

[12]  D. M. Rector,et al.  Optically teasing apart neural swelling and depolarization , 2007, Neuroscience.

[13]  B. He,et al.  Multimodal Functional Neuroimaging: Integrating Functional MRI and EEG/MEG , 2008, IEEE Reviews in Biomedical Engineering.

[14]  David A. Boas,et al.  Fast optical signal not detected in awake behaving monkeys , 2008, NeuroImage.

[15]  David A. Leopold,et al.  fMRI in the awake marmoset: Somatosensory-evoked responses, functional connectivity, and comparison with propofol anesthesia , 2013, NeuroImage.

[16]  L. Lemieux,et al.  Electrophysiological correlates of the BOLD signal for EEG‐informed fMRI , 2014, Human brain mapping.