Page 113 - ITU Journal Future and evolving technologies Volume 2 (2021), Issue 3 – Internet of Bio-Nano Things for health applications
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ITU Journal on Future and Evolving Technologies, Volume 2 (2021), Issue 3







            INFORMATION THEORETIC MODELING OF P ARANODAL REGIONS IN MYELINATED AXONS


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                                    Caglar Koca , Ozgur Ergul , Meltem Civas , Ozgur B. Akan 1,3
          1                                                                              2
          Internet of Everthing (IoE) Group, Department of Engineering, University of Cambridge, UK ,  Gazi University, Faculty of
                                                                                   3
            Engineering, Department of Electrical and Electronics Engineering, Ankara, Turkey,  Next‑generation and Wireless
                      Communications Laboratory (NWCL), Department of Electrical and Electronics Engineering,
                                               Koç University, Istanbul, Turkey
                                     NOTE: Corresponding author: Caglar Koca, ck542@cam.ac.uk

          Abstract – As a natural form of nanoscale communication, neuro‑spike communication inspires the deployment of nanoma‑
          chines inside the human body for healthcare. To this end, the identi ication of failure mechanisms in normal and diseased
          connections of nervous nano‑networks is crucial. Thus, in this paper, we investigate the information transmission through
          a single myelinated axon segment. We introduce a realistic multi‑compartmental model for a single myelinated segment
          by incorporating the axon’s paranodal regions to the model. Next, we characterize the myelinated segment communication
          channel in terms of attenuation over the range of frequencies. Based on this, we derive the rate per channel use and upper
          bound on the information capacity. The performance evaluations reveal that our approach provides dramatic correction re‑
          garding frequency response. We believe that this result could have a signi icant effect on the characterization of demyelinated
          axons from the information and communication technology (ICT) perspective.

          Keywords – ICT‑based treatment, intra‑body nano‑networks, Internet of Bio‑Nano Things, demyelination, neuro‑spike
          communication

          1.  INTRODUCTION                                     Regarding axonal transmission, communication and com‑
                                                               putational models of axons exist in the literature.  Com‑
          Advances in nanotechnology have opened the way for the  munication  models  mostly  assume  the  axon  as  an  ideal
          deployment of nanomachines collaborating within the In‑  all‑pass  ilter [8].  In biologically detailed communication
          ternet of Bio‑Nano Things (IoBNT) framework inside the  models, the axon is modeled as a low‑pass  ilter, and mod‑
          human body as a new means of information and com‑      ied  second‑order  Butterworth    ilters  [9,  10].  In  more
          munication technology (ICT)‑based treatment technique  complex models, axonal propagation is represented with
          [1, 2]. IoBNT offers both the abstraction necessary for a  several state transitions in the case of hippocampal pyra‑
          deeper look into the evolution of intra‑body communica‑  midal  neurons  [11].  Moreover,  an    inite  transmission
          tions [3] and the foundation for analyzing and interacting  line model is also available [12].  The limitations of com‑
          with living organisms. For example, as a large scale intra‑  munication models include that they cannot fully capture
          body nano‑network, the human nervous system bears an  the behavior of axons, which arises from the axon’s phys‑
          enormous potential to inspire architectures for such sys‑  iology.  The  computational  models,  on  the  other  hand,
          tems with novel applications in diverse areas, including  are  accepted  as  biologically  accurate.  Thus,  computa‑
          smart healthcare [4].                                tional models can be used to construct the realistic chan‑
                                                               nel model of axons, enabling accurate analyses. In this re‑
          Shannon’s information theory is usually applied to ex‑  spect,  multi‑compartment  models  successfully  describe
          isting intra‑body nano‑networks to analyze intra‑body  the axonal transmission by dividing an axonal cable into
          communication mechanisms, one of which is neuro‑spike  compartments,  where  each  compartment  has  the  same
          communication achieved via molecules [5]. Neuro‑spike  membrane properties [13].  However,  this approach ne‑
          communication consists of consecutive stages, namely,  glects some parts of the axon,  e.g.,  paranodal regions of
          spike generation, axonal and synaptic transmission. Un‑  myelinated  axons,  where  the  membrane  properties  are
          derstanding of communication failures within any of  not uniform.
          these stages due to nervous system diseases such as
          spinal cord injury and Multiple Sclerosis (MS) is crucial  In  many  vertebrates,  an  insulating  substance  called
          to the designs of assistive or replacement nanomachines  myelin sheath surrounds axons. The myelin sheath is the
          [6]. Accordingly, an accurate communication theoret‑  extension  of  the  plasma  membrane  of  glial  cells  wrap‑
          ical analysis of intra‑body communication channels re‑  ping the axon, possibly in a multilayered structure. Myelin
          quires realistic channel modeling of healthy and diseased  sheaths are formed in periodic segments.  The short por‑
          connections, which is promising in understanding dis‑  tions of the axon left uncovered by myelin are called the
          ease mechanisms in biological systems communicating  nodes  of  Ranvier.  Axonal  transmission  is  achieved  by
          via molecules [7].





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