Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Kim, Hojeong | - |
dc.date.available | 2017-08-10T08:10:30Z | - |
dc.date.created | 2017-08-09 | - |
dc.date.issued | 2017-07 | - |
dc.identifier.issn | 8750-7587 | - |
dc.identifier.uri | http://hdl.handle.net/20.500.11750/4140 | - |
dc.description.abstract | Persistent inward current (PIC)- generating Cav1.3 channels in spinal motoneuron dendrites are thought to be actively recruited during normal behaviors. However, whether and how the activation of PIC channels influences force output of motor unit remains elusive. Here, building a physiologically realistic model of slow motor unit I demonstrated that force production induced by the PIC activation is much smaller for short than lengthened muscles during the regular firing of the motoneuron that transitions from the quiescent state by either a brief current pulse at the soma or a brief synaptic excitation at the dendrites. By contrast, the PIC-induced force potentiation was maximal for short muscles when the motoneuron switched from a stable low-frequency firing state to a stable high-frequency firing state by the current pulse at the soma. Under the synaptic excitation at the dendrites, however, the force could not be potentiated by the transitioning of the motoneuron from a low- to a high-frequency firing state due to the simultaneous onset of PIC at the dendrites and firing at the soma. The strong dependency of the input-output relationship of the motor unit on the neuromodulation and Ia afferent inputs for the PIC channels was further shown under static variations in muscle length. Taken together, these findings suggest that the PIC activation in the motoneuron dendrites may differentially affect the force production of the motor unit, depending not only on the firing state history of the motoneuron and the variation in muscle length but also on the mode of motor activity. NEW & NOTEWORTHY Cav1.3 channels in motoneuron dendrites are actively involved during normal motor activities. To investigate the effects of the activation of motoneuron Cav1.3 channels on force production, a model motor unit was built based on best-available data. The simulation results suggest that force potentiation induced by Cav1.3 channel activation is strongly modulated not only by firing history of the motoneuron but also by length variation of the muscle as well as neuromodulation inputs from the brainstem. Copyright © 2017 the American Physiological Society. | - |
dc.language | English | - |
dc.publisher | American Physiological Society | - |
dc.title | Muscle length-dependent contribution of motoneuron Ca(v)1.3 channels to force production in model slow motor unit | - |
dc.type | Article | - |
dc.identifier.doi | 10.1152/japplphysiol.00491.2016 | - |
dc.identifier.scopusid | 2-s2.0-85021878500 | - |
dc.identifier.bibliographicCitation | Journal of Applied Physiology, v.123, no.1, pp.88 - 105 | - |
dc.subject.keywordAuthor | spinal motoneuron | - |
dc.subject.keywordAuthor | dendritic excitability | - |
dc.subject.keywordAuthor | L-type Ca channel | - |
dc.subject.keywordAuthor | force potentiation | - |
dc.subject.keywordAuthor | motor unit | - |
dc.subject.keywordPlus | Alpha Motoneurons | - |
dc.subject.keywordPlus | Cat Soleus Muscle | - |
dc.subject.keywordPlus | Dendritic Excitability | - |
dc.subject.keywordPlus | Dynamic Model | - |
dc.subject.keywordPlus | Force Potentiation | - |
dc.subject.keywordPlus | Frog Skeletal Muscle | - |
dc.subject.keywordPlus | In Vivo | - |
dc.subject.keywordPlus | L Type Ca Channel | - |
dc.subject.keywordPlus | Medial Gastrocnemius | - |
dc.subject.keywordPlus | Motor Unit | - |
dc.subject.keywordPlus | Persistent Inward Currents | - |
dc.subject.keywordPlus | Plateau Like Behavior | - |
dc.subject.keywordPlus | Spinal Motoneuron | - |
dc.subject.keywordPlus | Spinal Motoneurons | - |
dc.subject.keywordPlus | Systematic Variations | - |
dc.citation.endPage | 105 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 88 | - |
dc.citation.title | Journal of Applied Physiology | - |
dc.citation.volume | 123 | - |
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