A new model of the myelinated nerve fiber I s presented. The model assumes a tiaxial cable form, with separate noal, paranoal and interoal regions, a myelin sheath indepndent of the underlying interoal membrane and a periaxonal conductance pathway. The mel uses ionic channel dynamics for te mammal and 3mphibian derived from rcent experimental studies.
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A Distributed-parameter Model of the Myelinated Nerve Fiber
A new model of the myelinated nerve fiber I s presented. The model assumes a tiaxial cable form, with separate noal, paranoal and interoal regions, a myelin sheath indepndent of the underlying interoal membrane and a periaxonal conductance pathway. The mel uses ionic channel dynamics for te mammal and 3mphibian derived from rcent experimental studies.
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A new model of the myelinated nerve fiber I s presented. The model assumes a tiaxial cable form, with separate noal, paranoal and interoal regions, a myelin sheath indepndent of the underlying interoal membrane and a periaxonal conductance pathway. The mel uses ionic channel dynamics for te mammal and 3mphibian derived from rcent experimental studies.
Direitos autorais:
Attribution Non-Commercial (BY-NC)
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Baixe no formato PDF, TXT ou leia online no Scribd
John P.18lOt8n0JOn Y.L!mk, 1t. Department of Electrical and Computer Engineering Rice Univerity P.O. Box I82,Houston, Tx 772\ A new 00buIed paametr moel of the myelinated nerve fiber i s presented. Te model assumes a tiaxial cable form, with separate noal, paranoal and interoal regions, a myelin sheath indepndent of the underlying interoal membrane and a periaxonal conductance pathway. Um previous coaxial cable equivalent models, this new tiaxial form alSo allows for inclusion of ionic channels into the inter noal membI3ue. The mel uses ionic channel dynamics for te mammal and 3mphibi an derived from rcent experimental studies. The model reproduces conduction behavior seen in exprimental and previ ous modeling efforts. Most imprtantly, the moel reprouces the deplarizing 8l|I0nIta\ described by several i nvestigators whIch may have signicance in determination of the bchavIorofthe nerve fiber as m0Itpe action plcnuals are conducted or as multe stimuli are impsed. This aftertential cannot be produced by me previous coaxial models. The infuece of the characteristcs of the myelin sheat, underlying interodal membrane ad the priaxonal conduc tance pathway on the behavior of the neIVe fbe is explored. Previous models of m myelinated nerve fber were based on a coaxial cable equivalent rpresentation which assumed that the interodal region of the nere fibr could be segmented into passive lumped paralleled conductances and capacitances. This assumption cannot be made if the periaxonal space is to be con sidered and the myelin sheath is to be represented independent of the interodal membrane. Therefore a traxial cable equivalent form was assumed, consisting of an extacellular, intracellular and periaxonal longitudinal conductive pathways and separate transverse pathways representng the myelin and m membrane beneat. A transverse conductance was also included, represent ing the nodal gap region just outside the active node of Ranvier. Nol PGenUal (mV) ISO ~ . - o : - -1- - - , - -_ I - - -1- - - I I I I -1- - - . ---1 - _1 __ _ i Nol Gap PocaU_1 (mV) 0.1 -1---._- O ~~ ".1 - - - I ___ 1 _ _ _ , I I I -0.4 . - _| - __ . __ L__ _ _ -_ I i I e.+
Transmembrane Potenllal (mV)
-+--- 1 -4--{
,, - - : ---1--- I I 1 ___ 1 __ _ I I TransmyeUn Poenllal (mV) 1-----<-- 0- - - 10 Figure 1: Temporal plolof the top8gating action ptential at memid- pont ofthe nerve fiber. Recent studies have examined the dynamics of m ionic channels in the amphibian and mammalian myelinated nerve fi ber in the nodal as well as the interodal regions. In order to produce a model based on the most recent exprimental data available, these dynamics were included in the model. In the cases where only experimental data was available, a Marquardt non-linear parameter estimation method was used to ft the steady-state and time constant relations describing te ionic channel kinetics to the data. An implicit integration technique was employed to solve for m system of equarions reprsenting te nerve fiber. An example of the behavior of the model can be seen in fgures I and 2. Figure is an example of a propagating action ptential vs. time as seen across the node, nodal gap, myelin and intero dal membrane. ou the presence of most of the potential across the myelin sheath which has the greater impedance. Also note the presence of a depolarizing afterptential at the node and across the interodal membrane. In fgure 2 the spatal distn'bu tion of the action potential across the myelin sheath and the underlying membrane can be seen. The fiber was stimulated at the right end, propagaton is from right t left. In conclusion, this new triaxial model allows for a detailed functional representaton of the myelinated nerve fber. Both the mammalian and amphibian nere fbers can be represented. The model generates propagating action potentals that correlate with measured potentials as well as previous modeling results. In additon, the model prduces deplarizing aferpotentials as seen in experimental studies which cannot be produced by previous coaxial nerve fber models. This work supported in pan by NSF Lrant EC&4064J6. Traommranc Poential (mV) ......... ... ::ujII I I , I I I 50 ! i 0 .1 s:lj(m) 0.6 0.8 FIgure 2: Spatial plot of the propagating CtIon ptential at O.3r after stimaIation. IEEE ENGINEERING IN MEDICINE & BIOLGY SOCIETY 10TH ANNUAL INTERATIONAL CONFERENCE--1923 CH2566-8/88/0000--1923 $1.00 0 1988 IEEE