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1 Misalignments between external and internal rhythms traduce, in the short term, into decrements of mental and physical health.- + 387 word(s) 387 2020-04-08 11:06:44 |
2 format correct + 1 word(s) 388 2020-11-01 10:49:42 |

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Behn, C.; De Gregorio, N. Rhythm Generation. Encyclopedia. Available online: https://encyclopedia.pub/entry/553 (accessed on 26 December 2024).
Behn C, De Gregorio N. Rhythm Generation. Encyclopedia. Available at: https://encyclopedia.pub/entry/553. Accessed December 26, 2024.
Behn, Claus, Nicole De Gregorio. "Rhythm Generation" Encyclopedia, https://encyclopedia.pub/entry/553 (accessed December 26, 2024).
Behn, C., & De Gregorio, N. (2020, April 11). Rhythm Generation. In Encyclopedia. https://encyclopedia.pub/entry/553
Behn, Claus and Nicole De Gregorio. "Rhythm Generation." Encyclopedia. Web. 11 April, 2020.
Rhythm Generation
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Rhythms are essential to living beings. They allow fluxes to coordinate with one another. Rhythms, thereby, constitute an information system for body functions. Biosphere rhythmicity largely relates to geophysical oscillations. To ignore the latter also affects human health and performance.

biological rhythms geophysical oscillations metabolic fluxes human health and performance

1. Introduction

Life implicates and depends on rhythms. Energy flowing through living beings generates linear and/or cyclic deviations from thermodynamic equilibrium  [1] "Nondecaying, repetitive phenomena", or cycles, determine the chemical organization of living matter [2]. Cycles also occur in simple organic chemical processes like the Belousov-Zhabotinskii reaction [3]. Oscillatory reactions often involve positive free enthalpy (Durup, 1979 cited by [4]). An oscillating signal requiring less energy implicates a gain in precision of control [5]. Biological control based on periodical events, thus, becomes energetically more advantageous and more efficient than that relying on steady-state reactions [5]. Phased with the environment at more or less constant period length, endogenous oscillators influence the genome [6] and by means of the latter, also affect functions like cell growth, protein synthesis, stress responses, and intermediary metabolism [7]. Timekeeping of energy metabolism and related body functions is mostly under the control of transcriptionally based, cell autonomous mechanisms in step with post-translational processes. Interlocked by transcriptional feedback loops, gene products like CLOCK and BMAL1 drive biological clocks positively, while others like CRY1-2, PER1-3 and REV-ERBα do it negatively [6][8][7][9]. Individual phase differences in PER3 expression, thus, correlate with timing of sleep during a constant routine [10].

2. Mechanisms 

The mechanisms by which the multiple feedback loops are integrated remain largely to be specified. Uncertain are also the post-translational mechanisms possibly involved in clock regulation [11][12][13][14]. Clock components (such as BMAL1 and CLOCK) may, moreover, additionally affect gene expression and metabolic processes, apparently not related to their proper timing function [15][16]. The mechanism by which clock protein stability connects with circadian period length is not yet exactly known [17]. Clinical consequences of period shortening in circadian cycles are evidenced in sleeping sickness caused by Trypanosoma brucei [18]. Noticeably, however, cycling also occurs in the absence of a genome, as shown by intracellular K+ levels in human red cells [19]. However rhythms are caused, they allow the necessary time keeping in living beings, or as having stated by Joseph Bass (2017): As energy metabolism being in constant flux, there would be time in biochemical processes, as there is in a central train station [20].

References

  1. Schrödinger, E.. What is Life? The Physical Aspect of the Living Cell; Cambridge Univ. Press: Cambridge, UK, 1944; pp. ..
  2. Krebs, H.. Reminiscences and Reflections; Oxford University Press: Oxford, UK, 1981; pp. ..
  3. Semenov, S.N.; Kraft, L.J.; Ainla, A.; Zhao, M.; Baghbanzadeh, M.; Campbell, V.E.; Kang, K.; Fox, J.M.; Whitesides, G.M.; Autocatalytic, bistable, oscillatory networks of biologically relevant organic reactions. Nature 2016, 537, 656-660.
  4. Hess, B.; The glycolytic oscillator. J. Exp. Biol 1979, 81, 7-14.
  5. Rapp, P.; Why are so many biological systems periodic?. Prog. Neurobiol. 1987, 29, 261-273.
  6. Sassone-Corsi, P.; Molecular clocks: Mastering time by gene regulation. Nature 1998, 392, 871-874.
  7. Cedernaes, J.; Waldeck, N.; Bass, J.; Neurogenetic basis for circadian regulation of metabolism by the hypothalamus.. Genes Dev 2019, 33, 1136-1158.
  8. Rijo-Ferreira, F.; Takahashi, J.S.; Genomics of circadian rhythms in health and disease. Genome Med 2019, 11, 82.
  9. Hatanaka, F.; Matsubara, C.; Myung, J.; Yoritaka, T.; Kamimura, N.; Tsutsumi, S.; Kanai, A.; Suzuki, Y.; Sassone-Corsi, P.; Aburatani, H.; et al.et al. Genome-Wide Profiling of the Core Clock Protein BMAL1 Targets Reveals a Strict Relationship with Metabolism.. Mol. Cell. Biol. 2010, 30, 5636-5648.
  10. Archer, S.; Viola, A.; Kyriakopoulou, V.; Von Schantz, M.; Dijk, D.; Inter-Individual Di erences in Habitual Sleep Timing and Entrained Phase of Endogenous Circadian Rhythms of BMAL1, PER2 and PER3 mRNA in Human Leukocytes.. Sleep 2008, 31, 608-617.
  11. Gorman, M.R.; Temporal organization of pineal melatonin signaling in mammals.. Mol. Cell. Endocrinol. 2020, 503, 110687.
  12. Zheng, X.; Sehgal, A.; Probing the relative importance of molecular oscillations in the circadian clock.. Genetics 2008, 178, 1147–1155.
  13. Rutkowski D Thomas; Hegde Ramanujan; Regulation of basal cellular physiology by the homeostatic unfolded protein response. Journal of Cell Biology 2010, 189, 783-794, 10.1083/jcb.201003138.
  14. Golombek, D.A.; Rosenstein, R.E.; Physiology of circadian entrainment. Physiol. Rev. 2010, 90, 1063-1102.
  15. McGinnis Graham; Young Martin E; Circadian regulation of metabolic homeostasis: causes and consequences. Nature and Science of Sleep 2016, 8, 163-180, 10.2147/NSS.S78946.
  16. Spanagel R; Pendyala G; Abarca C; Zghoul T; Sanchis-Segura C; Magnone MCM; Lascorz J; Depner M; Holzberg D; Soyka M; et al.Schreiber SMatsuda FLathrop MSchumann GAlbrecht U The clock gene Per2 influences the glutamatergic system and modulates alcohol consumption. Nature Medicine 2005, 11, 35-42.
  17. Dunlap Jay C.; Loros Jennifer J.; Making Time: Conservation of Biological Clocks from Fungi to Animals. Microbiology Spectrum 2017, 5, 1-19, 10.1128/microbiolspec.funk-0039-2016.
  18. Rijo-Ferreira, F.; Carvalho, T.; Afonso, C.; Sanches-Vaz, M.; Costa, R.M.; Figueiredo, L.M.; Takahashi, J.S.; Sleeping sickness is a circadian disorder. Nat. Commun. 2018, 9 , 1–13.
  19. Henslee, E.A.; Crosby, P.; Kitcatt, S.J.; Parry, J.S.W.; Bernardini, A.; Abdallat, R.G.; Braun, G.; Fatoyinbo, H.O.; Harrison, E.J.; Edgar, R.S.; et al.et al. Rhythmic potassium transport regulates the circadian clock in human red blood cells. . Nat. Commun. 2017, 8, 1–10.
  20. Bass, J.T.; The circadian clock system’s influence in health and disease. . Genome Med. 2017, 9, 1–5.
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