Intrinsic heterogeneity in oscillatory dynamics limits correlation-induced neural synchronization

被引:42
|
作者
Burton, Shawn D. [3 ]
Ermentrout, G. Bard [2 ,3 ]
Urban, Nathaniel N. [1 ,3 ]
机构
[1] Carnegie Mellon Univ, Dept Biol Sci, Mellon Inst, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Dept Math, Pittsburgh, PA 15260 USA
[3] Ctr Neural Basis Cognit, Pittsburgh, PA USA
基金
美国安德鲁·梅隆基金会; 美国国家科学基金会;
关键词
phase-response curve; stochastic synchrony; neural oscillators; biophysical diversity; olfaction; PHASE-RESPONSE CURVES; OLFACTORY-BULB; ELECTRICAL SYNAPSES; CHOLINERGIC NEUROMODULATION; ODOR; INFORMATION; MODULATION; NEURONS; CELLS; REPRESENTATIONS;
D O I
10.1152/jn.00362.2012
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Burton SD, Ermentrout GB, Urban NN. Intrinsic heterogeneity in oscillatory dynamics limits correlation-induced neural synchronization. J Neurophysiol 108: 2115-2133, 2012. First published July 18, 2012; doi: 10.1152/jn.00362.2012.-Synchronous neural oscillations are found throughout the brain and are thought to contribute to neural coding and the propagation of activity. Several proposed mechanisms of synchronization have gained support through combined theoretical and experimental investigation, including mechanisms based on coupling and correlated input. Here, we ask how correlation-induced synchrony is affected by physiological heterogeneity across neurons. To address this question, we examined cell-to-cell differences in phase-response curves (PRCs), which characterize the response of periodically firing neurons to weak perturbations. Using acute slice electrophysiology, we measured PRCs across a single class of principal neurons capable of sensory-evoked oscillations in vivo: the olfactory bulb mitral cells (MCs). Periodically firing MCs displayed a broad range of PRCs, each of which was well fit by a simple three-parameter model. MCs also displayed differences in firing rate-current relationships and in preferred firing rate ranges. Both the observed PRC heterogeneity and moderate firing rate differences (similar to 10 Hz) separately reduced the maximum correlation-induced synchrony between MCs by up to 25-30%. Simulations further demonstrated that these components of heterogeneity alone were sufficient to account for the difference in synchronization among heterogeneous vs. homogeneous populations in vitro. Within this simulation framework, independent modulation of specific PRC features additionally revealed which aspects of PRC heterogeneity most strongly impact correlation-induced synchronization. Finally, we demonstrated good agreement of novel mathematical theory with our experimental and simulation results, providing a theoretical basis for the influence of heterogeneity on correlation-induced neural synchronization.
引用
收藏
页码:2115 / 2133
页数:19
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