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An Analysis of the Transitions Between Down and Up States of the Cortical Slow Oscillation Under Urethane Anaesthesia

Overview
Journal J Biol Phys
Specialty Biophysics
Date 2009 Dec 5
PMID 19960241
Citations 6
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Abstract

We study the dynamics of the transition between the low- and high-firing states of the cortical slow oscillation by using intracellular recordings of the membrane potential from cortical neurons of rats. We investigate the evidence for a bistability in assemblies of cortical neurons playing a major role in the maintenance of this oscillation. We show that the trajectory of a typical transition takes an approximately exponential form, equivalent to the response of a resistor-capacitor circuit to a step-change in input. The time constant for the transition is negatively correlated with the membrane potential of the low-firing state, and values are broadly equivalent to neural time constants measured elsewhere. Overall, the results do not strongly support the hypothesis of a bistability in cortical neurons; rather, they suggest the cortical manifestation of the oscillation is a result of a step-change in input to the cortical neurons. Since there is evidence from previous work that a phase transition exists, we speculate that the step-change may be a result of a bistability within other brain areas, such as the thalamus, or a bistability among only a small subset of cortical neurons, or as a result of more complicated brain dynamics.

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References
1.
Timofeev I, Grenier F, Bazhenov M, Sejnowski T, Steriade M . Origin of slow cortical oscillations in deafferented cortical slabs. Cereb Cortex. 2000; 10(12):1185-99. DOI: 10.1093/cercor/10.12.1185. View

2.
Steyn-Ross D, Steyn-Ross M, Sleigh J, Wilson M, Gillies I, Wright J . The sleep cycle modelled as a cortical phase transition. J Biol Phys. 2013; 31(3-4):547-69. PMC: 3456332. DOI: 10.1007/s10867-005-1285-2. View

3.
Steriade M, Nunez A, Amzica F . Intracellular analysis of relations between the slow (< 1 Hz) neocortical oscillation and other sleep rhythms of the electroencephalogram. J Neurosci. 1993; 13(8):3266-83. PMC: 6576520. View

4.
Hill S, Tononi G . Modeling sleep and wakefulness in the thalamocortical system. J Neurophysiol. 2004; 93(3):1671-98. DOI: 10.1152/jn.00915.2004. View

5.
Wilson M, Barry M, Reynolds J, Hutchison E, Steyn-Ross D . Characteristics of temporal fluctuations in the hyperpolarized state of the cortical slow oscillation. Phys Rev E Stat Nonlin Soft Matter Phys. 2008; 77(6 Pt 1):061908. DOI: 10.1103/PhysRevE.77.061908. View