Computer model for action potential propagation through branch point in myelinated nerves

被引:54
作者
Zhou, L [1 ]
Chiu, SY [1 ]
机构
[1] Univ Wisconsin, Sch Med, Dept Physiol, Madison, WI 53706 USA
关键词
D O I
10.1152/jn.2001.85.1.197
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A mathematical model is developed for simulation of action potential propagation through a single branch point of a myelinated nerve fiber with a parent branch bifurcating into two identical daughter branches. This model is based on a previously published multi-layer compartmental model for single unbranched myelinated nerve fibers. Essential modifications were made to couple both daughter branches to the parent branch. There are two major features in this model. First, the model could incorporate detailed geometrical parameters for the myelin sheath and the axon, accomplished by dividing both structures into many segments. Second, each segment has two layers, the myelin sheath and the axonal membrane, allowing voltages of intra-axonal space and periaxonal space to be calculated separately. In this model, K ion concentration in the periaxonal space is dynamically linked to the activity of axonal fast K channels underneath the myelin in the paranodal region. Our model demonstrates that the branch point acts like a low-pass filter, blocking high-frequency transmission from the parent to the daughter branches. Theoretical analysis showed that the cutoff frequency for transmission through the branch point is determined by temperature, local K ion accumulation, width of the periaxonal space, and internodal lengths at the vicinity of the branch point. Our result is consistent with empirical findings of irregular spacing of nodes of Ranvier at axon abors, suggesting that branch points of myelinated axons play important roles in signal integration in an axonal tree.
引用
收藏
页码:197 / 210
页数:14
相关论文
共 57 条
[1]  
[Anonymous], METHODS NEURAL MODEL
[2]   K+ ACCUMULATION IN THE SPACE BETWEEN GIANT-AXON AND SCHWANN-CELL IN THE SQUID ALLOTEUTHIS - EFFECTS OF CHANGES IN OSMOLARITY [J].
ASTION, ML ;
COLES, JA ;
ORKAND, RK ;
ABBOTT, NJ .
BIOPHYSICAL JOURNAL, 1988, 53 (02) :281-285
[3]   INTRACELLULAR-RECORDING FROM VERTEBRATE MYELINATED AXONS - MECHANISM OF THE DEPOLARIZING AFTERPOTENTIAL [J].
BARRETT, EF ;
BARRETT, JN .
JOURNAL OF PHYSIOLOGY-LONDON, 1982, 323 (FEB) :117-144
[4]   CHANGES IN EXCITABILITY OF HUMAN MOTOR AXONS UNDERLYING POSTISCHEMIC FASCICULATIONS - EVIDENCE FOR 2 STABLE STATES [J].
BOSTOCK, H ;
BAKER, M ;
REID, G .
JOURNAL OF PHYSIOLOGY-LONDON, 1991, 441 :537-557
[5]   POSTTETANIC EXCITABILITY CHANGES AND ECTOPIC DISCHARGES IN A HUMAN MOTOR AXON [J].
BOSTOCK, H ;
BERGMANS, J .
BRAIN, 1994, 117 :913-928
[6]  
Chiu S. Y., 1995, P777
[7]   POTASSIUM CHANNELS IN NODAL AND INTERNODAL AXONAL MEMBRANE OF MAMMALIAN MYELINATED FIBERS [J].
CHIU, SY ;
RITCHIE, JM .
NATURE, 1980, 284 (5752) :170-171
[8]   FUNCTIONS AND DISTRIBUTION OF VOLTAGE-GATED SODIUM AND POTASSIUM CHANNELS IN MAMMALIAN SCHWANN-CELLS [J].
CHIU, SY .
GLIA, 1991, 4 (06) :541-558
[9]   Excitability of the squid giant axon revisited [J].
Clay, JR .
JOURNAL OF NEUROPHYSIOLOGY, 1998, 80 (02) :903-913
[10]   ACTIVITY-DEPENDENT K+ ACCUMULATION IN THE DEVELOPING RAT OPTIC-NERVE [J].
CONNORS, BW ;
RANSOM, BR ;
KUNIS, DM ;
GUTNICK, MJ .
SCIENCE, 1982, 216 (4552) :1341-1343