Reuse & Permissions

It is not necessary to obtain permission to reuse this article or its components as it is available under the terms of the Creative Commons Attribution 4.0 International license. This license permits unrestricted use, distribution, and reproduction in any medium, provided attribution to the author(s) and the published article's title, journal citation, and DOI are maintained. Please note that some figures may have been included with permission from other third parties. It is your responsibility to obtain the proper permission from the rights holder directly for these figures.

Export citation

Export citation

Choose format for download:

Download Citation
  • Open Access
  • Access by Xinjiang University

Combined effects of spike-timing-dependent plasticity and homeostatic structural plasticity on coherence resonance

Marius E. Yamakou1,2,* and Christian Kuehn3,4,†

  • 1Department of Data Science, Friedrich-Alexander-Universität Erlangen-Nürnberg, Cauerstr. 11, 91058 Erlangen, Germany
  • 2Max-Planck-Institut für Mathematik in den Naturwissenschaften, Inselstr. 22, 04103 Leipzig, Germany
  • 3Faculty of Mathematics, Technical University of Munich, Boltzmannstrasse 3, 85748 Garching bei München, Germany
  • 4Complexity Science Hub Vienna, Josefstädter Strasse 39, 1080 Vienna, Austria

  • *marius.yamakou@fau.de
  • ckuehn@ma.tum.de

Phys. Rev. E 107, 044302 – Published 13 April, 2023

DOI: https://doi.org/10.1103/PhysRevE.107.044302

Abstract

Efficient processing and transfer of information in neurons have been linked to noise-induced resonance phenomena such as coherence resonance (CR), and adaptive rules in neural networks have been mostly linked to two prevalent mechanisms: spike-timing-dependent plasticity (STDP) and homeostatic structural plasticity (HSP). Thus this paper investigates CR in small-world and random adaptive networks of Hodgkin-Huxley neurons driven by STDP and HSP. Our numerical study indicates that the degree of CR strongly depends, and in different ways, on the adjusting rate parameter P, which controls STDP, on the characteristic rewiring frequency parameter F, which controls HSP, and on the parameters of the network topology. In particular, we found two robust behaviors. (i) Decreasing P (which enhances the weakening effect of STDP on synaptic weights) and decreasing F (which slows down the swapping rate of synapses between neurons) always leads to higher degrees of CR in small-world and random networks, provided that the synaptic time delay parameter τc has some appropriate values. (ii) Increasing the synaptic time delay τc induces multiple CR (MCR)—the occurrence of multiple peaks in the degree of coherence as τc changes—in small-world and random networks, with MCR becoming more pronounced at smaller values of P and F. Our results imply that STDP and HSP can jointly play an essential role in enhancing the time precision of firing necessary for optimal information processing and transfer in neural systems and could thus have applications in designing networks of noisy artificial neural circuits engineered to use CR to optimize information processing and transfer.

View figure in article

Physics Subject Headings (PhySH)

Article Text

References (86)

  1. R. Benzi, G. Parisi, A. Sutera, and A. Vulpiani, Tellus 34, 10 (1982).
  2. Z. Hou, K. Qu, and H. Xin, ChemPhysChem 6, 58 (2005).
  3. P. Hänggi, ChemPhysChem 3, 285 (2002).
  4. W. Horsthemke and R. Lefever, Noise-Induced Transitions: Theory and Applications in Physics, Chemistry, and Biology (Springer, New York, 1984), p. 164.
  5. M. D. McDonnell and L. M. Ward, Nat. Rev. Neurosci. 12, 415 (2011).
  6. A. Longtin, J. Stat. Phys. 70, 309 (1993).
  7. B. J. Gluckman, P. So, T. I. Netoff, M. L. Spano, and S. J. Schiff, Chaos 8, 588 (1998).
  8. A. Bulsara, E. Jacobs, T. Zhou, F. Moss, and L. Kiss, J. Theor. Biol. 152, 531 (1991).
  9. C. B. Muratov, E. Vanden-Eijnden, and E. Weinan, Physica D 210, 227 (2005).
  10. M. E. Yamakou and T. D. Tran, Nonlinear Dyn. 107, 2847 (2022).
  11. M. E. Yamakou, E. Heinsalu, M. Patriarca, and S. Scialla, Phys. Rev. E 106, L032401 (2022).
  12. M. E. Yamakou and J. Jost, EPL (Europhys. Lett.) 120, 18002 (2017).
  13. B. S. Gutkin, J. Jost, and H. C. Tuckwell, Naturwissenschaften 96, 1091 (2009).
  14. A. Buchin, S. Rieubland, M. Häusser, B. S. Gutkin, and A. Roth, PLoS Comput. Biol. 12, e1005000 (2016).
  15. M. E. Yamakou and J. Jost, Biol. Cybern. 112, 445 (2018).
  16. A. S. Pikovsky and J. Kurths, Phys. Rev. Lett. 78, 775 (1997).
  17. M. E. Yamakou, T. D. Tran, and J. Jost, Front. Phys. 10, 909365 (2022).
  18. M. E. Yamakou and J. Jost, Phys. Rev. E 100, 022313 (2019).
  19. M. E. Yamakou and E. M. Inack, Nonlinear Dyn. 111, 7789 (2023).
  20. B. Vázquez-Rodríguez, A. Avena-Koenigsberger, O. Sporns, A. Griffa, P. Hagmann, and H. Larralde, Sci. Rep. 7, 1 (2017).
  21. X. Sun, M. Perc, Q. Lu, and J. Kurths, Chaos 18, 023102 (2008).
  22. L. Lu, Y. Jia, M. Ge, Y. Xu, and A. Li, Nonlinear Dyn. 100, 877 (2020).
  23. Z. Gao, B. Hu, and G. Hu, Phys. Rev. E 65, 016209 (2001).
  24. D. Guo and C. Li, Phys. Rev. E 79, 051921 (2009).
  25. C. Liu, J. Wang, H. Yu, B. Deng, K. Tsang, W. Chan, and Y. Wong, Commun. Nonlinear Sci. Numer. Simul. 19, 1088 (2014).
  26. M. Gosak, D. Korošak, and M. Marhl, Phys. Rev. E 81, 056104 (2010).
  27. R. Toral, C. Mirasso, and J. Gunton, Europhys. Lett. 61, 162 (2003).
  28. N. Semenova and A. Zakharova, Chaos 28, 051104 (2018).
  29. H. C. Tuckwell and J. Jost, J. Comput. Neurosci. 30, 361 (2011).
  30. M. Uzuntarla, E. Barreto, and J. J. Torres, PLoS Comput. Biol. 13, e1005646 (2017).
  31. E. Yilmaz, M. Uzuntarla, M. Ozer, and M. Perc, Physica A 392, 5735 (2013).
  32. Q. Wang, M. Perc, Z. Duan, and G. Chen, Chaos 19, 023112 (2009).
  33. E. Yilmaz, V. Baysal, and M. Ozer, Phys. Lett. A 379, 1594 (2015).
  34. A. Zamani, N. Novikov, and B. Gutkin, Commun. Nonlinear Sci. Numer. Simul. 82, 105024 (2020).
  35. L. Gammaitoni, M. Löcher, A. Bulsara, P. Hänggi, J. Neff, K. Wiesenfeld, W. Ditto, and M. E. Inchiosa, Phys. Rev. Lett. 82, 4574 (1999).
  36. B. J. Gluckman, T. I. Netoff, E. J. Neel, W. L. Ditto, M. L. Spano, and S. J. Schiff, Phys. Rev. Lett. 77, 4098 (1996).
  37. S. Sinha and B. K. Chakrabarti, Phys. Rev. E 58, 8009 (1998).
  38. S. Zambrano, J. M. Casado, and M. A. Sanjuán, Phys. Lett. A 366, 428 (2007).
  39. S. Sinha, Physica A 270, 204 (1999).
  40. S. Nobukawa and N. Shibata, Sci. Rep. 9, 1 (2019).
  41. W. Gerstner, R. Kempter, J. L. Van Hemmen, and H. Wagner, Nature (London) 383, 76 (1996).
  42. H. Markram, J. Lübke, M. Frotscher, and B. Sakmann, Science 275, 213 (1997).
  43. A. Morrison, A. Aertsen, and M. Diesmann, Neural Comput. 19, 1437 (2007).
  44. W. T. Greenough and C. H. Bailey, Trends Neurosci. 11, 142 (1988).
  45. A. Van Ooyen and M. Butz-Ostendorf, The Rewiring Brain: A Computational Approach to Structural Plasticity in the Adult Brain (Academic Press, New York, 2017).
  46. S. H. Bennett, A. J. Kirby, and G. T. Finnerty, Neurosci. Biobehav. Rev. 88, 51 (2018).
  47. H. Ko, L. Cossell, C. Baragli, J. Antolik, C. Clopath, S. B. Hofer, and T. D. Mrsic-Flogel, Nature (London) 496, 96 (2013).
  48. A. Holtmaat and K. Svoboda, Nat. Rev. Neurosci. 10, 647 (2009).
  49. C. C. Hilgetag and A. Goulas, Brain Struct. Funct. 221, 2361 (2016).
  50. M. Valencia, J. Martinerie, S. Dupont, and M. Chavez, Phys. Rev. E 77, 050905(R) (2008).
  51. G. Turrigiano, Cold Spring Harbor Perspect. Biol. 4, a005736 (2012).
  52. M. Butz, I. D. Steenbuck, and A. van Ooyen, Front. Synaptic Neurosci. 6, 7 (2014).
  53. K. Pozo and Y. Goda, Neuron 66, 337 (2010).
  54. A. J. Watt and N. S. Desai, Front. Syn. Neurosci. 2, 5 (2010).
  55. M. N. Galtier and G. Wainrib, Neural Comput. 25, 2815 (2013).
  56. B. Jia, H.-G. Gu, and Y.-Y. Li, Chin. Phys. Lett. 28, 090507 (2011).
  57. H. Yu, X. Guo, J. Wang, B. Deng, and X. Wei, Physica A 419, 307 (2015).
  58. H. Xie, Y. Gong, and Q. Wang, Eur. Phys. J. B 89, 1 (2016).
  59. H. Xie, Y. Gong, and B. Wang, Chaos Solitons Fractals 108, 1 (2018).
  60. R. FitzHugh, Biophys. J. 1, 445 (1961).
  61. A. L. Hodgkin and A. F. Huxley, J. Physiol. 117, 500 (1952).
  62. R. F. Fox, Biophys. J. 72, 2068 (1997).
  63. J. A. White, J. T. Rubinstein, and A. R. Kay, Trends Neurosci. 23, 131 (2000).
  64. D. J. Watts and S. H. Strogatz, Nature (London) 393, 440 (1998).
  65. G.-q. Bi and M.-m. Poo, J. Neurosci. 18, 10464 (1998).
  66. D. E. Feldman and M. Brecht, Science 310, 810 (2005).
  67. S. Song, K. D. Miller, and L. F. Abbott, Nat. Neurosci. 3, 919 (2000).
  68. D. S. Bassett and E. Bullmore, Neuroscientist 12, 512 (2006).
  69. X. Liao, A. V. Vasilakos, and Y. He, Neurosci. Biobehav. Rev. 77, 286 (2017).
  70. D. S. Bassett, A. Meyer-Lindenberg, S. Achard, T. Duke, and E. Bullmore, Proc. Natl. Acad. Sci. USA 103, 19518 (2006).
  71. S. F. Muldoon, E. W. Bridgeford, and D. S. Bassett, Sci. Rep. 6, 1 (2016).
  72. S. Rakshit, B. K. Bera, D. Ghosh, and S. Sinha, Phys. Rev. E 97, 052304 (2018).
  73. M. Masoliver, N. Malik, E. Schöll, and A. Zakharova, Chaos 27, 101102 (2017).
  74. X. Pei, L. Wilkens, and F. Moss, Phys. Rev. Lett. 77, 4679 (1996).
  75. D. J. Higham, SIAM Rev. 43, 525 (2001).
  76. Q. Ren, K. M. Kolwankar, A. Samal, and J. Jost, Phys. Rev. E 86, 056103 (2012).
  77. O. V. Popovych, S. Yanchuk, and P. A. Tass, Sci. Rep. 3, 1 (2013).
  78. F. Gabbiani and C. Koch, Principles of spike train analysis, in Methods in Neuronal Modeling From Ions to Networks, edited by C. Koch and I. Segev (The MIT Press, Cambridge, MA, 1998), p.313.
  79. Y. Gong, M. Wang, Z. Hou, and H. Xin, ChemPhysChem 6, 1042 (2005).
  80. A. Neiman, P. I. Saparin, and L. Stone, Phys. Rev. E 56, 270 (1997).
  81. J. Hizanidis and E. Schöll, Phys. Rev. E 78, 066205 (2008).
  82. H. Gu, H. Zhang, C. Wei, M. Yang, Z. Liu, and W. Ren, Int. J. Mod. Phys. B 25, 3977 (2011).
  83. Z. Brzosko, S. B. Mierau, and O. Paulsen, Neuron 103, 563 (2019).
  84. W. M. Pardridge, J. Cereb. Blood Flow Metab. 32, 1959 (2012).
  85. S. Panzeri, E. Janotte, A. Pequeño-Zurro, J. Bonato, and C. Bartolozzi, Neuromorph. Comput. Eng. 3, 012001 (2023).
  86. S. P. Eberhardt, T. Duong, and A. Thakoor, in Proceedings of the Third Annual Parallel Processing Symposium (IEEE, New York, 1989), Vol. 1, pp. 257–267.

Outline

Information

Sign In to Your Journals Account

Filter

Filter

Article Lookup

Enter a citation