Abstract
The study addressed the problem of information transmission in mammalian brain as reflected in the emergence or disappearence of temporal patterns in extra-cellularly monitored single action potentials from the dorsal hippocampus of unrestrained cats during slow wave sleep (SWS), rapid eye movement sleep (REM), and motionless quiet wakefulness (QW). The spike trains were analyzed with a non-paarametric technique. Chi-square statistics were used to measure deviations of firing patterns from the theoretical model which is based on the assumption that the intervals are random and/or independent from each other. The plots of the chi-square values for a given set of patterns represented the neuronal ‘signatures’ characteristic a behavioral state. During SWS most neurons followed the theoretical model, i.e. their ‘signatures’ were flat and statistically non-significant. However, during REM sleep and QW their firing modes showed specific deviations from the theoretical model: some patters occured more often while others less often than expected, thus generating large and statistically significant ‘signatures’. During REM sleep some neurons shared similar tendencies in their departures from the theoretical model. However, during QW the same neurons developed their individual ‘signatures’ which were significantly different from each other. Hence, the QW episodes were characterized by a greater differentiation of neuronal firing patterns. The mean firing rate and the shape of the time interval histogramwere not necessarily correlated with the emergence of specific temporal patterns in spike trains. The results suggest that information transmission from one neuron to anothe depends on the emergence of repetitive and specific temporal patterns. The strong tendency of most neurons to lapse during SWS into a firing mode that closely follows the theoretical model constitutes the basis for a working hypothesis which states that the essence of SWS recovery processes in cognitive systems is the disappearance of temporal patterns, and that the ‘noisy’ interactions between neurons plays an important role in the recuperative processes.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.