. Neuroelectric oscillations reflect rhythmic fluctuations of neuronal ensembles between high and low excitability states. These fluctuations clearly impact on sensory processing and cognitive operations, but their actual utility is unclear. Our broad goal is to explore the overarching hypothesis that low frequency neuronal oscillations can function as """"""""instruments"""""""" for active selection of task-relevant inputs in visual cortex and for enhancement of their representation across processing stages. A key proposition of this hypothesis is that in dealing adaptively with ever-changing tasks, ranging from rhythmic (e.g., watching a person walking by) to random (e.g., waiting for a traffic light to change), the brain shifts dynamically between """"""""rhythmic"""""""" and """"""""continuous"""""""" modes of operation. This proposition makes specific predictions vis-?-vis neuronal oscillations, and these will be explored by """"""""paired"""""""" linear array multielectrode recordings from V1 and extrastriate visual cortices in awake- behaving monkeys. We have 3 specific aims.
Aim 1 : investigate the mechanistic role of neuronal oscillations in inter-modal attention. Expt 1 will build on our earlier studies on intermodal selective attention (b.2.a;c.2.1). Specific new predictions will be tested using behavioral measures, along with laminar current source density and multiunit activity profiles sampled during task performance using linear array multielectrodes positioned in V1, V4 and inferotemporal (IT) cortex. Inter-areal interactions (prediction 4) will be evaluated using dual multielectrode recordings.
Aim 2 : evaluate the generality of oscillatory involvement in attentional function and dysfunction. Generalization of finding outside of intermodal selection is important to establish because most selective attention investigations focus on effects within one sensory modality. Thus, Expt 2 will use a visual feature- attention task. To maintain comparability, stimulus manipulations, recording methods and tests of predictions will otherwise generally parallel those of Expt 1. The paradigm in Expt 2 is adapted from studies examining the neurophysiology of attentional deficits in schizophrenia. Expt 2 thus has additional translational value, in that it can determine the physiological significance of ERP components and/or oscillatory characteristics that are shown to be abnormal under corresponding conditions in schizophrenia (b.3;b.5;b.6).
Aim 3 : investigate the relevance of rhythmic mode processing in natural vision. Expt 3 will use a visual search paradigm, along with a match to sample paradigm, to evaluate the hypotheses that: 1) the key feature of rhythmic mode processing, the rhythmic fluctuation of neuronal excitability, is also a dominant feature in natural visual behavior, and 2) that this is due, at least in part, to the rhythmic nature of visual (saccade/fixation) sampling behavior, and the powerful organizing effects of fixation onset on cortical oscillatory activity (c.2.3). Expt 3 will also examine effects of fixation onset on oscillatory synchrony across cortical layers and across cortical areas.

Public Health Relevance

A fundamental theme of our research program is a close integration of basic visual-cognitive neuroscience in monkeys, with ERP and fMRI investigations comparing normal function with neuropsychiatric dysfunction in patients with schizophrenia. This translational emphasis will be reflected in this competing renewal proposal.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH060358-13
Application #
8479214
Study Section
Special Emphasis Panel (ZRG1-IFCN-L (02))
Program Officer
Rossi, Andrew
Project Start
2000-05-01
Project End
2014-05-31
Budget Start
2013-06-01
Budget End
2014-05-31
Support Year
13
Fiscal Year
2013
Total Cost
$372,676
Indirect Cost
$124,027
Name
Nathan Kline Institute for Psychiatric Research
Department
Type
DUNS #
167204762
City
Orangeburg
State
NY
Country
United States
Zip Code
10962
Sherman, Maxwell A; Lee, Shane; Law, Robert et al. (2016) Neural mechanisms of transient neocortical beta rhythms: Converging evidence from humans, computational modeling, monkeys, and mice. Proc Natl Acad Sci U S A 113:E4885-94
Kajikawa, Yoshinao; Schroeder, Charles E (2015) Generation of field potentials and modulation of their dynamics through volume integration of cortical activity. J Neurophysiol 113:339-51
Haegens, Saskia; Barczak, Annamaria; Musacchia, Gabriella et al. (2015) Laminar Profile and Physiology of the ? Rhythm in Primary Visual, Auditory, and Somatosensory Regions of Neocortex. J Neurosci 35:14341-52
Morillon, Benjamin; Hackett, Troy A; Kajikawa, Yoshinao et al. (2015) Predictive motor control of sensory dynamics in auditory active sensing. Curr Opin Neurobiol 31:230-8
van Atteveldt, Nienke; Musacchia, Gabriella; Zion-Golumbic, Elana et al. (2015) Complementary fMRI and EEG evidence for more efficient neural processing of rhythmic vs. unpredictably timed sounds. Front Psychol 6:1663
Morillon, Benjamin; Schroeder, Charles E; Wyart, Valentin (2014) Motor contributions to the temporal precision of auditory attention. Nat Commun 5:5255
Lakatos, Peter; Musacchia, Gabriella; O'Connel, Monica N et al. (2013) The spectrotemporal filter mechanism of auditory selective attention. Neuron 77:750-61
Zion Golumbic, Elana M; Ding, Nai; Bickel, Stephan et al. (2013) Mechanisms underlying selective neuronal tracking of attended speech at a ""cocktail party"". Neuron 77:980-91
Lakatos, Peter; Schroeder, Charles E; Leitman, David I et al. (2013) Predictive suppression of cortical excitability and its deficit in schizophrenia. J Neurosci 33:11692-702
Schroeder, Charles E; Lakatos, Peter (2012) The signs of silence. Neuron 74:770-2

Showing the most recent 10 out of 32 publications