Characterization and modeling of intermittent locomotor dynamics in clock gene-deficient mice.

The scale-invariant and intermittent dynamics of animal behavior are attracting scientific interest. Recent findings concerning the statistical laws of behavioral organization shared between healthy humans and wild-type mice (WT) and their alterations in human depression patients and circadian clock...

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Main Authors: Toru Nakamura, Toru Takumi, Atsuko Takano, Fumiyuki Hatanaka, Yoshiharu Yamamoto
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3596351?pdf=render
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spelling doaj-78bbc9198a3a4f9193f17b5e1e4167122020-11-25T01:19:08ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0183e5888410.1371/journal.pone.0058884Characterization and modeling of intermittent locomotor dynamics in clock gene-deficient mice.Toru NakamuraToru TakumiAtsuko TakanoFumiyuki HatanakaYoshiharu YamamotoThe scale-invariant and intermittent dynamics of animal behavior are attracting scientific interest. Recent findings concerning the statistical laws of behavioral organization shared between healthy humans and wild-type mice (WT) and their alterations in human depression patients and circadian clock gene (Period 2; Per2) mutant mice indicate that clock genes play functional roles in intermittent, ultradian locomotor dynamics. They also claim the clinical and biological importance of the laws as objective biobehavioral measures or endophenotypes for psychiatric disorders. In this study, to elucidate the roles of breakdown of the broader circadian regulatory circuit in intermittent behavioral dynamics, we studied the statistical properties and rhythmicity of locomotor activity in Per2 mutants and mice deficient in other clock genes (Bmal1, Clock). We performed wavelet analysis to examine circadian and ultradian rhythms and estimated the cumulative distributions of resting period durations during which locomotor activity levels are continuously lower than a predefined threshold value. The wavelet analysis revealed significant amplification of ultradian rhythms in the BMAL1-deficient mice, and instability in the Per2 mutants. The resting period distributions followed a power-law form in all mice. While the distributions for the BMAL1-deficient and Clock mutant mice were almost identical to those for the WT mice, with no significant differences in their parameter (power-law scaling exponent), only the Per2 mutant mice showed consistently and significantly lower values of the scaling exponent, indicating the increased intermittency in ultradian locomotor dynamics. Furthermore, based on a stochastic priority queuing model, we explained the power-law nature of resting period distributions, as well as its alterations shared with human depressive patients and Per2 mutant mice. Our findings lead to the development of a novel mathematical model for abnormal behaviors in psychiatric disorders.http://europepmc.org/articles/PMC3596351?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Toru Nakamura
Toru Takumi
Atsuko Takano
Fumiyuki Hatanaka
Yoshiharu Yamamoto
spellingShingle Toru Nakamura
Toru Takumi
Atsuko Takano
Fumiyuki Hatanaka
Yoshiharu Yamamoto
Characterization and modeling of intermittent locomotor dynamics in clock gene-deficient mice.
PLoS ONE
author_facet Toru Nakamura
Toru Takumi
Atsuko Takano
Fumiyuki Hatanaka
Yoshiharu Yamamoto
author_sort Toru Nakamura
title Characterization and modeling of intermittent locomotor dynamics in clock gene-deficient mice.
title_short Characterization and modeling of intermittent locomotor dynamics in clock gene-deficient mice.
title_full Characterization and modeling of intermittent locomotor dynamics in clock gene-deficient mice.
title_fullStr Characterization and modeling of intermittent locomotor dynamics in clock gene-deficient mice.
title_full_unstemmed Characterization and modeling of intermittent locomotor dynamics in clock gene-deficient mice.
title_sort characterization and modeling of intermittent locomotor dynamics in clock gene-deficient mice.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description The scale-invariant and intermittent dynamics of animal behavior are attracting scientific interest. Recent findings concerning the statistical laws of behavioral organization shared between healthy humans and wild-type mice (WT) and their alterations in human depression patients and circadian clock gene (Period 2; Per2) mutant mice indicate that clock genes play functional roles in intermittent, ultradian locomotor dynamics. They also claim the clinical and biological importance of the laws as objective biobehavioral measures or endophenotypes for psychiatric disorders. In this study, to elucidate the roles of breakdown of the broader circadian regulatory circuit in intermittent behavioral dynamics, we studied the statistical properties and rhythmicity of locomotor activity in Per2 mutants and mice deficient in other clock genes (Bmal1, Clock). We performed wavelet analysis to examine circadian and ultradian rhythms and estimated the cumulative distributions of resting period durations during which locomotor activity levels are continuously lower than a predefined threshold value. The wavelet analysis revealed significant amplification of ultradian rhythms in the BMAL1-deficient mice, and instability in the Per2 mutants. The resting period distributions followed a power-law form in all mice. While the distributions for the BMAL1-deficient and Clock mutant mice were almost identical to those for the WT mice, with no significant differences in their parameter (power-law scaling exponent), only the Per2 mutant mice showed consistently and significantly lower values of the scaling exponent, indicating the increased intermittency in ultradian locomotor dynamics. Furthermore, based on a stochastic priority queuing model, we explained the power-law nature of resting period distributions, as well as its alterations shared with human depressive patients and Per2 mutant mice. Our findings lead to the development of a novel mathematical model for abnormal behaviors in psychiatric disorders.
url http://europepmc.org/articles/PMC3596351?pdf=render
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AT torutakumi characterizationandmodelingofintermittentlocomotordynamicsinclockgenedeficientmice
AT atsukotakano characterizationandmodelingofintermittentlocomotordynamicsinclockgenedeficientmice
AT fumiyukihatanaka characterizationandmodelingofintermittentlocomotordynamicsinclockgenedeficientmice
AT yoshiharuyamamoto characterizationandmodelingofintermittentlocomotordynamicsinclockgenedeficientmice
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