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Neural generators of early cortical somatosensory evoked potentials in the awake monkey
Affiliation:1. Department of Neuroscience, Albert Einstein College of Medicine, Rose Fitzgerald Kennedy Center, Room 322, 1300 Morris Park Ave., Bronx, NY 10461, USA;2. Department of Neurology, Albert Einstein College of Medicine, Rose Fitzgerald Kennedy Center, Room 322, 1300 Morris Park Ave., Bronx, NY 10461, USA;1. Research Group Modulation of Language Networks, Department of Neuropsychology, Max Planck Institute for Human Cognitive and Brain Sciences Leipzig, Leipzig, Germany;2. Department of Psychiatry, Psychotherapy and Psychosomatics, Medical Faculty, RWTH Aachen, Aachen, Germany;3. JARA-BRAIN, Jülich-Aachen Research Alliance, Germany;4. Parietal Team, INRIA, Neurospin, Gif-sur-Yvette, France;1. Barrow Neurological Institute, Division of Neurosurgery, Phoenix, Arizona, USA;2. Scripps Clinic, La Jolla, California, USA;3. San Diego Center for Spinal Disorders, La Jolla, California, USA;1. Department of Neurosurgery, Johns Hopkins Hospital, Baltimore, MD, United States;2. Department of Neurosurgery, Barrow Neurological Institute, Saint Joseph’s Hospital and Medical Center, Phoenix, AZ, United States;1. General Surgery, Sisli Hamidiye Etfal Education & Research Hospital, Istanbul, Turkey;2. General Surgery, Bahcesehir University, Istanbul, Turkey
Abstract:Controversy continues to exist regarding the generators of the initial cortical components of the somatosensory evoked potential (SEP). This issue was explored by detailed epidural and intracortical mapping of somatosensory evoked activity in Old World monkeys. In depth recordings, 3 complementary procedures were utilized: (1) the intracortical and subcortical distribution of SEPs was determined from approximately 4000 locations; (2) concomitant profiles of multiple unit activity (MUA) were recorded as an estimate of local action potential profiles; (3) 1-dimensional calculations of current source density (CSD) were used to outline the timing and pattern of regional transmembrane current flow. Our analysis confirms the participation of multiple cortical areas, located on either side of the central sulcus, in the generation of the initial cortical SEP components. Earliest activity, P10, was localized to area 3, followed within milliseconds by activation of areas 1, 2 (P12), and 4 (P13). In SI (Brodmann's areas 3, 1 and 2), the initial SEP components reflect the depolarization of lamina 4 stellate cells and the subsequent activation of adjacent pyramidal cells in laminae 3 and 5. The genesis of later cortical components (P20, N45) represents the composite of activity distributed across multiple cortical laminae and the interaction of overlapping excitatory and inhibitory events. These findings have direct implications for the clinical interpretation of SEP waveforms.
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