• DocumentCode
    2735559
  • Title

    Modeling of the suprachiasmatic nucleus based on reduced molecular clock mechanisms

  • Author

    Nakao, M. ; Nishmura, Y. ; Aoki, K. ; Katayama, N.

  • Author_Institution
    Graduate Sch. of Inf. Sci., Tohoku Univ., Sendai, Japan
  • Volume
    2
  • fYear
    2004
  • fDate
    1-5 Sept. 2004
  • Firstpage
    2897
  • Lastpage
    2900
  • Abstract
    One of the physiological substrates of circadian rhythms is known to be located in the suprachiasmatic nucleus (SCN), which unilaterally contains up to 10,000 or more pacemaker cells. Specific molecular clock mechanisms are working within each cell. Here, in order to prevent complexity explosion in understanding the dynamics of SCN, the molecular clock mechanisms are modeled in a reduced form preserving their dynamical characteristics. The reduced cellular models are coupled by diffusions of activating and suppressing agents so as to construct the whole SCN model. The resulting spatial patterns of entrainment are studied under varied diffusion constants. The simulation results suggest validity of reduction of the molecular dynamics as well as usefulness of the strategy employed to model the hierarchical biological system.
  • Keywords
    biochemistry; biodiffusion; cellular biophysics; genetics; molecular biophysics; physiological models; circadian rhythms; clock genes; diffusion constants; hierarchical biological system; molecular dynamics; pacemaker cells; physiological substrates; reduced cellular models; reduced molecular clock mechanisms; suprachiasmatic nucleus dynamical characteristics; suprachiasmatic nucleus modeling; Biological system modeling; Biological systems; Circadian rhythm; Clocks; Explosions; Mutual coupling; Oscillators; Pacemakers; Proteins; Temperature; clock gene; phase response curve; reaction-diffusion;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Engineering in Medicine and Biology Society, 2004. IEMBS '04. 26th Annual International Conference of the IEEE
  • Conference_Location
    San Francisco, CA
  • Print_ISBN
    0-7803-8439-3
  • Type

    conf

  • DOI
    10.1109/IEMBS.2004.1403824
  • Filename
    1403824