|
|
||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
1 Volen Center for Complex Systems, Brandeis University, Waltham, MA, USA; Department of Neurobiology, Duke University Medical Center, Durham, NC, USA
2 Volen Center for Complex Systems, Brandeis University, Waltham, MA, USA; Department of Biology, Brandeis University, Waltham, MA, USA
3 Department of Neurosurgery, Children's Hospital, Boston, MA, USA; Department of Psychology, University of Pennsylvania, Philadelphia, PA, USA
4 Department of Neurosurgery, Children's Hospital, Boston, MA, USA
5 Department of Neurology, Brigham and Women's Hospital, Boston, MA, USA
6 Department of Psychology, University of Pennsylvania, Philadelphia, PA, USA
* To whom correspondence should be addressed. E-mail: kahana{at}psych.upenn.edu.
Cortical theta appears important in sensory processing and memory. Intracanial electrode recordings provide a high spatial resolution method for studying such oscillations during cognitive tasks. Recent work revealed sites at which oscillations in the theta range (4-12Hz) could be gated by a working memory task: theta power was increased at task onset and continued until task offset. Using a large data set that has now been collected (10 participants/619 recording sites), we now have sufficient sampling to determine how these gated sites are distributed in the cortex and how they are synchronized. A substantial fraction of sites in occipital/parietal (45/157) and temporal (23/280) cortices were gated by the task. Surprisingly, this aspect of working memory function was virtually absent in frontal cortex (2/182). Coherence measures were used to analyze the synchronization of oscillations. We suspected that because of their coordinate regulation by the working memory task, gated sites would have synchronized theta oscillations. We found that whereas nearby gated sites (<20mm) were generally coherent, distant gated sites were almost never coherent. Our results imply that there are local mechanisms for the generation of cortical theta.
This article has been cited by other articles:
![]() |
E. E. Fanselow, K. A. Richardson, and B. W. Connors Selective, State-Dependent Activation of Somatostatin-Expressing Inhibitory Interneurons in Mouse Neocortex J Neurophysiol, November 1, 2008; 100(5): 2640 - 2652. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. J. Uhlhaas, C. Haenschel, D. Nikolic, and W. Singer The Role of Oscillations and Synchrony in Cortical Networks and Their Putative Relevance for the Pathophysiology of Schizophrenia Schizophr Bull, September 1, 2008; 34(5): 927 - 943. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. A. Meltzer, H. P. Zaveri, I. I. Goncharova, M. M. Distasio, X. Papademetris, S. S. Spencer, D. D. Spencer, and R. T. Constable Effects of Working Memory Load on Oscillatory Power in Human Intracranial EEG Cereb Cortex, August 1, 2008; 18(8): 1843 - 1855. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Jacobs, M. J. Kahana, A. D. Ekstrom, and I. Fried Brain Oscillations Control Timing of Single-Neuron Activity in Humans J. Neurosci., April 4, 2007; 27(14): 3839 - 3844. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH |
| Visit Other APS Journals Online |