Population activity in auditory cortex of the awake rat revealed by recording with dense microelectrode array

Cortical mechanisms of auditory perception include temporal interaction between neuronal ensembles in a functional cortical structure such as a place code of frequency, or tonotopic map. To investigate the mechanism, a recording method is needed to densely map spatio-temporal activity pattern within the predefined tonotopic organization specifically in the awake condition. The present study has proposed and developed an experimental system that is capable of simultaneous neural recording with a grid array of 100 sites with 400-μm inter-electrode distance in the 4th layer of auditory cortex of awake rat. Both multiunit activities (MUA) and local field potentials (LFPs) confirmed the tonotopic map in the auditory cortex. In addition, spectral powers in higher frequency components (4-120 Hz) were enhanced and a lower frequency component (1-4 Hz) was reduced during waking. Phase synchronization between recording sites in the gamma-band oscillatory activity was generally smaller in the awake cortex than in the anesthetized cortex. These results have proven the feasibility of our recording and will open a new avenue to investigate neural activities in the functional map of awake cortex.

[1]  Shaowen Bao,et al.  Early experience impairs perceptual discrimination , 2007, Nature Neuroscience.

[2]  David S. Greenberg,et al.  Population imaging of ongoing neuronal activity in the visual cortex of awake rats , 2008, Nature Neuroscience.

[3]  H. Read,et al.  Multiparametric auditory receptive field organization across five cortical fields in the albino rat. , 2007, Journal of neurophysiology.

[4]  W. Marsden I and J , 2012 .

[5]  V. Galhardo,et al.  Comparison of Anesthetic Depth Indexes Based on Thalamocortical Local Field Potentials in Rats , 2010, Anesthesiology.

[6]  N. Weinberger,et al.  Characterisation of multiple physiological fields within the anatomical core of rat auditory cortex , 2003, Hearing Research.

[7]  D A Steyn-Ross,et al.  Comparison of changes in electroencephalographic measures during induction of general anaesthesia: influence of the gamma frequency band and electromyogram signal. , 2001, British journal of anaesthesia.

[8]  Craig T. Nordhausen,et al.  Single unit recording capabilities of a 100 microelectrode array , 1996, Brain Research.

[9]  H. Kose,et al.  Learning-stage-dependent, field-specific, map plasticity in the rat auditory cortex during appetitive operant conditioning , 2011, Neuroscience.

[10]  T. Sejnowski,et al.  Thalamocortical oscillations in the sleeping and aroused brain. , 1993, Science.

[11]  Takeshi Ogawa,et al.  Large-Scale Heterogeneous Representation of Sound Attributes in Rat Primary Auditory Cortex: From Unit Activity to Population Dynamics , 2011, The Journal of Neuroscience.

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

[13]  W. Singer,et al.  The gamma cycle , 2007, Trends in Neurosciences.

[14]  E. Capaldi,et al.  The organization of behavior. , 1992, Journal of applied behavior analysis.

[15]  G. G. Stokes "J." , 1890, The New Yale Book of Quotations.

[16]  O. Chever,et al.  Cortical Inhibition during Burst Suppression Induced with Isoflurane Anesthesia , 2009, The Journal of Neuroscience.

[17]  M. Castro-Alamancos,et al.  Neocortex network activation and deactivation states controlled by the thalamus. , 2010, Journal of neurophysiology.

[18]  D. Contreras,et al.  Synchronization of fast (30-40 Hz) spontaneous cortical rhythms during brain activation , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.