Cellularly-Driven Differences in Network Synchronization Propensity Are Differentially Modulated by Firing Frequency 英文参考文献.docVIP
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Cellularly-Driven Differences in Network Synchronization Propensity Are Differentially Modulated by Firing Frequency 英文参考文献
Cellularly-DrivenDifferencesinNetworkSynchronization
PropensityAreDifferentiallyModulatedbyFiring
Frequency
ChristianG.Fink1*,VictoriaBooth2.,MichalZochowski1,3.
1Department of Physics, University of Michigan, Ann Arbor, Michigan, United States of America, 2Departments of Mathematics and Anesthesiology, University of
Michigan,AnnArbor,Michigan,UnitedStatesofAmerica,3BiophysicsProgram,UniversityofMichigan,AnnArbor,Michigan,UnitedStatesofAmerica
Abstract
Spatiotemporal pattern formation in neuronal networks depends on the interplay between cellular and network
synchronization properties. The neuronal phase response curve (PRC) is an experimentally obtainable measure that
characterizes the cellular response to small perturbations, and can serve as an indicator of cellular propensity for
synchronization.TwobroadclassesofPRCshavebeenidentifiedforneurons:TypeI,inwhichsmallexcitatoryperturbations
induceonlyadvancesinfiring,andTypeII,inwhichsmallexcitatoryperturbationscaninducebothadvancesanddelaysin
firing. Interestingly, neuronal PRCs are usually attenuated with increased spiking frequency, and Type II PRCs typically
exhibitagreaterattenuationofthephasedelayregionthanofthephaseadvanceregion.Wefoundthatthisphenomenon
arisesfromaninterplaybetweenthetimeconstantsofactiveioniccurrentsandtheinterspikeinterval.Asaresult,excitatory
networks consisting of neurons with Type I PRCs responded very differently to frequency modulation compared to
excitatorynetworkscomposedofneuronswithTypeIIPRCs.Specifically,increasedfrequencyinducedasharpdecreasein
synchronyofnetworksofTypeIIneurons,whilefrequencyincreasesonlyminimallyaffectedsynchronyinnetworksofType
Ineurons.Theseresultsaredemonstratedinnetworksinwhichbothtypesofneuronsweremodeledgenericallywiththe
Morris-Lecar model, as well as in networks consisting of Hodgkin-Huxley-based model cortical pyramidal cells in which
simulated effects of acetylcholine changed PRC type. These results are robust to different network structures, synapt
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