Phase-Amplitude Coupling in Spontaneous Mouse Behavior.

The level of activity of many animals including humans rises and falls with a period of ~ 24 hours. The intrinsic biological oscillator that gives rise to this circadian oscillation is driven by a molecular feedback loop with an approximately 24 hour cycle period and is influenced by the environment...

Full description

Bibliographic Details
Main Authors: Daniel Thengone, Khatuna Gagnidze, Donald Pfaff, Alex Proekt
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5025157?pdf=render
id doaj-8c7d9fca272a4609986817e90173c735
record_format Article
spelling doaj-8c7d9fca272a4609986817e90173c7352020-11-25T00:42:42ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-01119e016226210.1371/journal.pone.0162262Phase-Amplitude Coupling in Spontaneous Mouse Behavior.Daniel ThengoneKhatuna GagnidzeDonald PfaffAlex ProektThe level of activity of many animals including humans rises and falls with a period of ~ 24 hours. The intrinsic biological oscillator that gives rise to this circadian oscillation is driven by a molecular feedback loop with an approximately 24 hour cycle period and is influenced by the environment, most notably the light:dark cycle. In addition to the circadian oscillations, behavior of many animals is influenced by multiple oscillations occurring at faster-ultradian-time scales. These ultradian oscillations are also thought to be driven by feedback loops. While many studies have focused on identifying such ultradian oscillations, less is known about how the ultradian behavioral oscillations interact with each other and with the circadian oscillation. Decoding the coupling among the various physiological oscillators may be important for understanding how they conspire together to regulate the normal activity levels, as well in disease states in which such rhythmic fluctuations in behavior may be disrupted. Here, we use a wavelet-based cross-frequency analysis to show that different oscillations identified in spontaneous mouse behavior are coupled such that the amplitude of oscillations occurring at higher frequencies are modulated by the phase of the slower oscillations. The patterns of these interactions are different among different individuals. Yet this variability is not random. Differences in the pattern of interactions are confined to a low dimensional subspace where different patterns of interactions form clusters. These clusters expose the differences among individuals-males and females are preferentially segregated into different clusters. These sex-specific features of spontaneous behavior were not apparent in the spectra. Thus, our methodology reveals novel aspects of the structure of spontaneous animal behavior that are not observable using conventional methodology.http://europepmc.org/articles/PMC5025157?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Daniel Thengone
Khatuna Gagnidze
Donald Pfaff
Alex Proekt
spellingShingle Daniel Thengone
Khatuna Gagnidze
Donald Pfaff
Alex Proekt
Phase-Amplitude Coupling in Spontaneous Mouse Behavior.
PLoS ONE
author_facet Daniel Thengone
Khatuna Gagnidze
Donald Pfaff
Alex Proekt
author_sort Daniel Thengone
title Phase-Amplitude Coupling in Spontaneous Mouse Behavior.
title_short Phase-Amplitude Coupling in Spontaneous Mouse Behavior.
title_full Phase-Amplitude Coupling in Spontaneous Mouse Behavior.
title_fullStr Phase-Amplitude Coupling in Spontaneous Mouse Behavior.
title_full_unstemmed Phase-Amplitude Coupling in Spontaneous Mouse Behavior.
title_sort phase-amplitude coupling in spontaneous mouse behavior.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2016-01-01
description The level of activity of many animals including humans rises and falls with a period of ~ 24 hours. The intrinsic biological oscillator that gives rise to this circadian oscillation is driven by a molecular feedback loop with an approximately 24 hour cycle period and is influenced by the environment, most notably the light:dark cycle. In addition to the circadian oscillations, behavior of many animals is influenced by multiple oscillations occurring at faster-ultradian-time scales. These ultradian oscillations are also thought to be driven by feedback loops. While many studies have focused on identifying such ultradian oscillations, less is known about how the ultradian behavioral oscillations interact with each other and with the circadian oscillation. Decoding the coupling among the various physiological oscillators may be important for understanding how they conspire together to regulate the normal activity levels, as well in disease states in which such rhythmic fluctuations in behavior may be disrupted. Here, we use a wavelet-based cross-frequency analysis to show that different oscillations identified in spontaneous mouse behavior are coupled such that the amplitude of oscillations occurring at higher frequencies are modulated by the phase of the slower oscillations. The patterns of these interactions are different among different individuals. Yet this variability is not random. Differences in the pattern of interactions are confined to a low dimensional subspace where different patterns of interactions form clusters. These clusters expose the differences among individuals-males and females are preferentially segregated into different clusters. These sex-specific features of spontaneous behavior were not apparent in the spectra. Thus, our methodology reveals novel aspects of the structure of spontaneous animal behavior that are not observable using conventional methodology.
url http://europepmc.org/articles/PMC5025157?pdf=render
work_keys_str_mv AT danielthengone phaseamplitudecouplinginspontaneousmousebehavior
AT khatunagagnidze phaseamplitudecouplinginspontaneousmousebehavior
AT donaldpfaff phaseamplitudecouplinginspontaneousmousebehavior
AT alexproekt phaseamplitudecouplinginspontaneousmousebehavior
_version_ 1725280865362116608