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dc.contributor.author Kim, Hojeong ko
dc.date.available 2018-01-11T12:07:08Z -
dc.date.created 2018-01-01 -
dc.date.issued 2017-11 -
dc.identifier.citation Journal of Applied Physiology, v.123, no.5, pp.1166 - 1187 -
dc.identifier.issn 8750-7587 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/4848 -
dc.description.abstract The goal of this study is to investigate how the dendritic Ca-PIC location influences nonlinear input-output properties and depends on the type of motoneurons across the motoneuron pool. A model motoneuron pool consisting of 10 motoneurons was constructed using a recently developed two-compartment modeling approach that reflected key cell type-associated properties experimentally identified. The dendritic excitability and firing output depended systematically on both the PIC location and the motoneuron type. The PIC onset and offset in the current-voltage (I-V) relationship tended to occur at more hyperpolarized voltages as the path length to the PIC channels from the soma increased and as the cell type shifted from high- to lowthreshold motoneurons. At the same time, the firing acceleration and frequency hysteresis in the frequency-current (F-I) relationship became faster and larger, respectively. However, the PIC onset-offset hysteresis increased as the path length and the recruitment threshold increased. Furthermore, the gain of frequency-current function before full PIC activation was larger for PIC channels located over distal dendritic regions in low- compared with high-threshold motoneurons. When compared with previously published experimental observations, the modeling concurred when Ca-PIC channels were placed closer to the soma in high- than low-threshold motoneurons in the model motoneuron pool. All of these results suggest that the negative relationship of Ca-PIC location and cell recruitment threshold may underlie the systematic variation in I-V and F-I transformation across the motoneuron pool. NEW & NOTEWORTHY How does the dendritic location of calcium persistent inward current (Ca-PIC) influence dendritic excitability and firing behavior across the spinal motoneuron pool? This issue was investigated developing a model motoneuron pool that reflected key motoneuron type-specific properties experimentally identified. The simulation results point out the negative relationship between the distance of Ca-PIC source from the soma and cell recruitment threshold as a basis underlying the systematic variation in input-output properties of motoneurons over the motoneuron pool. © Copyright 2017 the American Physiological Society. -
dc.language English -
dc.publisher American Physiological Society -
dc.title Impact of the localization of dendritic calcium persistent inward current on the input-output properties of spinal motoneuron pool: a computational study -
dc.type Article -
dc.identifier.doi 10.1152/japplphysiol.00034.2017 -
dc.identifier.wosid 000416597900018 -
dc.identifier.scopusid 2-s2.0-85034026095 -
dc.type.local Article(Overseas) -
dc.type.rims ART -
dc.description.journalClass 1 -
dc.identifier.citationVolume 123 -
dc.identifier.citationNumber 5 -
dc.identifier.citationStartPage 1166 -
dc.identifier.citationEndPage 1187 -
dc.identifier.citationTitle Journal of Applied Physiology -
dc.type.journalArticle Article -
dc.description.isOpenAccess Y -
dc.subject.keywordAuthor computational modeling -
dc.subject.keywordAuthor dendritic calcium currents -
dc.subject.keywordAuthor nonlinear firing behavior -
dc.subject.keywordAuthor spinal motoneurons -
dc.subject.keywordAuthor motoneuron pool -
dc.subject.keywordPlus PLATEAU POTENTIALS -
dc.subject.keywordPlus IN-VIVO -
dc.subject.keywordPlus SYSTEMATIC VARIATIONS -
dc.subject.keywordPlus ELECTRICAL-PROPERTIES -
dc.subject.keywordPlus HINDLIMB MOTONEURONS -
dc.subject.keywordPlus INTRINSIC-PROPERTIES -
dc.subject.keywordPlus LUMBAR MOTONEURONS -
dc.subject.keywordPlus NEURON MODELS -
dc.subject.keywordPlus CAT -
dc.subject.keywordPlus BISTABILITY -
dc.contributor.affiliatedAuthor Kim, Hojeong -
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Division of Biotechnology 1. Journal Articles
Companion Diagnostics and Medical Technology Research Group 1. Journal Articles

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