Xenon and nitrous oxide induced changes in resting EEG activity can be explained by systematic increases in the relaxation rates of stochastically driven alpha band oscillatory activity.
Rick Evertz, Andria Pelentritou, John Cormack, Damien G Hicks, David T J Liley
Journal of neural engineering April 11, 2025 DOI: 10.1088/1741-2552/adc8d3 via PubMed
Summary
AI-generated from the abstractResting EEG activity typically resembles a filtered random process, and alpha band (8-13 Hz) oscillations can be modeled as independent, stochastically driven relaxation oscillators. This study tested whether changes in alpha band power and spectral slope during anesthesia with xenon and nitrous oxide—both NMDA receptor antagonists—could be explained by alterations in the distribution of alpha band damping rates. In participants receiving step-level increases of xenon (n=24) or nitrous oxide (n=20), both agents produced dose-dependent reductions in alpha power and spectral slope (15-40 Hz), accounted for by increased mean alpha band damping.
Study at a glance
| Characteristics | Experimental study Peer reviewed |
|---|---|
| Sample size | 44 |
| Population | Participants receiving equilibrated step-level increases in inhaled concentrations of xenon or nitrous oxide |
| Interventions | Xenon Nitrous oxide |
| Keywords | EEG Alpha band Damped relaxation oscillations Nitrous oxide Xenon |
| Key finding | Both xenon and nitrous oxide produce level-dependent reductions in alpha band power and spectral slope, accountable by increases in mean alpha band damping, suggesting mechanistic similarity consistent with NMDA receptor antagonism. |
Abstract
Objective. Resting electroencephalographic activity is typically indistinguishable from a filtered linear random process across a diverse range of behavioural and pharmacological states, suggesting that the power spectral density of the resting electroencephalogram (EEG) can be modelled as the superposition of multiple, stochastically driven and independent, alpha band (8-13 Hz) relaxation oscillators. This simple model can account for variations in alpha band power and '1/f scaling' in eyes-open/eyes-closed conditions in terms of alterations in the distribution of the alpha band oscillatory relaxation rates. As changes in alpha band power and '1/f scaling' have been reported in anaesthesia we hypothesise that such changes may also be accounted for by alterations in alpha band relaxation oscillatory rate distributions.Approach. On this basis we choose to study the EEG activity of xenon and nitrous oxide, gaseous anaesthetic agents that have been reported to produce different EEG effects, notable given they are both regarded as principally acting via N-methyl-D-aspartate (NMDA) receptor antagonism. By recording high density EEG from participants receiving equilibrated step-level increases in inhaled concentrations of xenon (n= 24) and nitrous oxide (n= 20), alpha band relaxation rate (damping) distributions were estimated by solving an inhomogeneous integral equation describing the linear superposition of multiple alpha-band relaxation oscillators having a continuous distribution of dampings.Main results. For both agents, level-dependent reductions in alpha band power and spectral slope exponent (15-40 Hz) were observed, that were accountable by increases in mean alpha band damping.Significance. These shared increases suggest that, consistent with their identified molecular targets of action, xenon and nitrous oxide are mechanistically similar, a conclusion further supported by neuronal population modelling in which NMDA antagonism is associated with increases in damping and reductions in peak alpha frequency. Alpha band damping may provide an important link between experiment and theories of consciousness, such as the global neuronal network theory, where the likelihood of a globally excited state ('conscious percept'), is inversely related to mean damping.