ArticleBiophysical journal2003
Kinetic diversity of single-channel burst openings underlying persistent Na(+) current in entorhinal cortex neurons.
Article in Biophysical journal, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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7 citing papers in PubMed, 11 citations in OpenAlex.
- Synergetic action of domain II and IV underlies persistent current generation in Nav1.3 as revealed by a tarantula toxin.Scientific reports · 2015Article
- Cell-attached single-channel recordings in intact prefrontal cortex pyramidal neurons reveal compartmentalized D1/D5 receptor modulation of the persistent sodium current.Frontiers in neural circuits · 2015Article
- Intrinsic electrophysiological properties of entorhinal cortex stellate cells and their contribution to grid cell firing fields.Frontiers in neural circuits · 2012Article
- Modulation of single-channel properties of TRPV1 by phosphorylation.The Journal of physiology · 2010Article
- Biophysical characterisation of the persistent sodium current of the Nav1.6 neuronal sodium channel: a single-channel analysis.Pflugers Archiv : European journal of physiology · 2010Article
- Kinetic and functional analysis of transient, persistent and resurgent sodium currents in rat cerebellar granule cells in situ: an electrophysiological and modelling study.The Journal of physiology · 2006Article
- Multiple conductance substates in pharmacologically untreated Na(+) channels generating persistent openings in rat entorhinal cortex neurons.The Journal of membrane biology · 2006Article
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Authors and funding
3 authors at 2 institutions in 2 countries.
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No grant is acknowledged in the PubMed record.
Abstract
The kinetic diversity of burst openings responsible for the persistent Na(+) current (I(NaP)) in entorhinal cortex neurons was examined by separately analyzing single bursts. Although remarkable kinetic variability was observed among bursts in terms of intraburst opening probability and mean open and closed times, the values of time constants describing intraburst open times (tau(o(b))s) and closed times (tau(c(b))s) were distributed around well-defined peaks. At -40 mV, tau(o(b)) peaks were found at approximately 0.34 (tau(o(b))1) and 0.77 (tau(o(b))2) ms, and major tau(c(b)) peaks were found at approximately 0.24 (tau(c(b))1) and 0.54 (tau(c(b))2) ms. In approximately 80% of the bursts two preferential gating modes were found that consisted of a combination of either tau(o(b))1 and tau(c(b))2 ("intraburst mode 1"), or tau(o(b))2 and tau(c(b))1 ("intraburst mode 2"). Individual channels could switch between different gating modalities, but normally tended to maintain a specific gating mode for long periods. Mean burst duration also displayed considerable variability. At least three time constants were found to describe burst duration, and the frequencies at which each of the corresponding "bursting states" occurred varied in different channels. Short-lasting bursting states were preferentially associated with intraburst mode 1, whereas very-long-lasting bursts tended to gate according to mode 2 only or other modes that included considerably longer mean open times. These results show that I(NaP) channels can generate multiple intraburst open and closed states and bursting states, but these different kinetic states tend to combine in definite ways to produce a limited number of prevalent, well-defined gating modalities. Modulation of distinct gating modalities in individual Na(+) channels may be a powerful form of plasticity to influence neuronal excitability and function.
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