Single-Trial Phase Precession in the Hippocampus

被引:92
作者
Schmidt, Robert [1 ,2 ]
Diba, Kamran [3 ]
Leibold, Christian [4 ]
Schmitz, Dietmar [2 ,5 ,6 ]
Buzsaki, Gyoergy [3 ]
Kempter, Richard [1 ,2 ,5 ,6 ]
机构
[1] Humboldt Univ, Dept Biol, Inst Theoret Biol, D-10115 Berlin, Germany
[2] Bernstein Ctr Computat Neurosci Berlin, D-10115 Berlin, Germany
[3] Rutgers State Univ, Ctr Mol & Behav Neurobiol, Newark, NJ 07102 USA
[4] Univ Munich, Dept Biol 2, D-82152 Planegg Martinsried, Germany
[5] Univ Med Berlin, Charite, Neurosci Res Ctr, D-10117 Berlin, Germany
[6] Univ Med Berlin, Charite, Neurocure Ctr Neurosci, D-10117 Berlin, Germany
基金
美国国家卫生研究院;
关键词
CELL ASSEMBLIES; THETA RHYTHM; PLACE CELLS; PYRAMIDAL CELLS; SEQUENCES; OSCILLATIONS; COMPRESSION; MECHANISMS; DYNAMICS; MODEL;
D O I
10.1523/JNEUROSCI.2270-09.2009
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
During the crossing of the place field of a pyramidal cell in the rat hippocampus, the firing phase of the cell decreases with respect to the local theta rhythm. This phase precession is usually studied on the basis of data in which many place field traversals are pooled together. Here we study properties of phase precession in single trials. We found that single-trial and pooled-trial phase precession were different with respect to phase-position correlation, phase-time correlation, and phase range. Whereas pooled-trial phase precession may span 360, the most frequent single-trial phase range was only similar to 180 degrees. In pooled trials, the correlation between phase and position (r = -0.58) was stronger than the correlation between phase and time (r = -0.27), whereas in single trials these correlations (r = -0.61 for both) were not significantly different. Next, we demonstrated that phase precession exhibited a large trial-to-trial variability. Overall, only a small fraction of the trial-to-trial variability in measures of phase precession (e. g., slope or offset) could be explained by other single-trial properties (such as running speed or firing rate), whereas the larger part of the variability remains to be explained. Finally, we found that surrogate single trials, created by randomly drawing spikes from the pooled data, are not equivalent to experimental single trials: pooling over trials therefore changes basic measures of phase precession. These findings indicate that single trials may be better suited for encoding temporally structured events than is suggested by the pooled data.
引用
收藏
页码:13232 / 13241
页数:10
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