On the origin of the extracellular action potential waveform:: A modeling study

被引:387
作者
Gold, C [1 ]
Henze, DA
Koch, C
Buzsáki, G
机构
[1] CALTECH, Beckman Inst, Pasadena, CA 91125 USA
[2] Merck Res Labs, West Point, PA USA
[3] Rutgers State Univ, Ctr Mol & Behav Neurosci, Newark, NJ 07102 USA
关键词
D O I
10.1152/jn.00979.2005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Although extracellular unit recording is typically used for the detection of spike occurrences, it also has the theoretical ability to report about what are typically considered intracellular features of the action potential. We address this theoretical ability by developing a model system that captures features of experimentally recorded simultaneous intracellular and extracellular recordings of CA1 pyramidal neurons. We use the line source approximation method of Holt and Koch to model the extracellular action potential (EAP) voltage resulting from the spiking activity of individual neurons. We compare the simultaneous intracellular and extracellular recordings of CA1 pyramidal neurons recorded in vivo with model predictions for the same cells reconstructed and simulated with compartmental models. The model accurately reproduces both the waveform and the amplitude of the EAPs, although it was difficult to achieve simultaneous good matches on both the intracellular and extracellular waveforms. This suggests that accounting for the EAP waveform provides a considerable constraint on the overall model. The developed model explains how and why the waveform varies with electrode position relative to the recorded cell. Interestingly, each cell's dendritic morphology had very little impact on the EAP waveform. The model also demonstrates that the varied composition of ionic currents in different cells is reflected in the features of the EAP.
引用
收藏
页码:3113 / 3128
页数:16
相关论文
共 59 条
[1]  
[Anonymous], 1998, THESIS CALTECH PASAD
[2]  
[Anonymous], 1969, BIOMAGNETIC PHENOMEN
[3]  
BORGGRAHAM LJ, CEREBRAL CORTEX, V13, P19
[4]   Pattern and inhibition-dependent invasion of pyramidal cell dendrites by fast spikes in the hippocampus in vivo [J].
Buzsaki, G ;
Penttonen, M ;
Nadasdy, Z ;
Bragin, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (18) :9921-9925
[5]   Somadendritic backpropagation of action potentials in cortical pyramidal cells of the awake rat [J].
Buzsáki, G ;
Kandel, A .
JOURNAL OF NEUROPHYSIOLOGY, 1998, 79 (03) :1587-1591
[6]   DIFFERENT CA2+ CHANNELS IN SOMA AND DENDRITES OF HIPPOCAMPAL PYRAMIDAL NEURONS MEDIATE SPIKE-INDUCED CA2+ INFLUX [J].
CHRISTIE, BR ;
ELIOT, LS ;
ITO, K ;
MIYAKAWA, H ;
JOHNSTON, D .
JOURNAL OF NEUROPHYSIOLOGY, 1995, 73 (06) :2553-2557
[7]  
Colbert CM, 1996, J NEUROSCI, V16, P6676
[8]  
Colbert CM, 1997, J NEUROSCI, V17, P6512
[9]   Ion channel properties underlying axonal action potential initiation in pyramidal neurons [J].
Colbert, CM ;
Pan, EH .
NATURE NEUROSCIENCE, 2002, 5 (06) :533-538
[10]   Massively parallel recording of unit and local field potentials with silicon-based electrodes [J].
Csicsvari, J ;
Henze, DA ;
Jamieson, B ;
Harris, KD ;
Sirota, A ;
Barthó, P ;
Wise, KD ;
Buzsáki, G .
JOURNAL OF NEUROPHYSIOLOGY, 2003, 90 (02) :1314-1323