Is Spreading Depolarization Characterized by an Abrupt, Massive Release of Gibbs Free Energy from the Human Brain Cortex?

Author:

Dreier Jens P.123,Isele Thomas4,Reiffurth Clemens13,Offenhauser Nikolas13,Kirov Sergei A.5,Dahlem Markus A.4,Herreras Oscar6

Affiliation:

1. Center for Stroke Research Berlin, Charité University Medicine Berlin, Berlin, Germany

2. Department of Neurology, Charité University Medicine Berlin, Berlin, Germany

3. Department of Experimental Neurology, Charité University Medicine Berlin, Berlin, Germany

4. Institute for Theoretical Physics, Technical University Berlin, Berlin, Germany

5. Department of Neurosurgery, Georgia Health Sciences University, Augusta, GA, USA

6. Department of Systems Neuroscience, Cajal Institute-CSIC, Madrid, Spain

Abstract

In the evolution of the cerebral cortex, the sophisticated organization in a steady state far away from thermodynamic equilibrium has produced the side effect of two fundamental pathological network events: ictal epileptic activity and spreading depolarization. Ictal epileptic activity describes the partial disruption, and spreading depolarization describes the near-complete disruption of the physiological double Gibbs–Donnan steady state. The occurrence of ictal epileptic activity in patients has been known for decades. Recently, unequivocal electrophysiological evidence has been found in patients that spreading depolarizations occur abundantly in stroke and brain trauma. The authors propose that the ion changes can be taken to estimate relative changes in Gibbs free energy from state to state. The calculations suggest that in transitions from the physiological state to ictal epileptic activity to spreading depolarization to death, the cortex releases Gibbs free energy in a stepwise fashion. Spreading depolarization thus appears as a twilight state close to death. Consistently, electrocorticographic recordings in the core of focal ischemia or after cardiac arrest display a smooth transition from the initial spreading depolarization component to the later ultraslow negative potential, which is assumed to reflect processes in cellular death.

Publisher

SAGE Publications

Subject

Neurology (clinical),General Neuroscience

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