Literature DB >> 17100843

Developmental expression of Na+ currents in mouse Purkinje neurons.

Mark Fry1.   

Abstract

As Purkinje neurons mature during postnatal development, they change from electrically quiescent to active and exhibit high frequency spontaneous action potentials. This change in electrical activity is determined by both alteration in ion channel expression and the acquisition of synaptic input. To gain a better understanding of the development the intrinsic electrical properties of these neurons, acutely isolated Purkinje neurons from mice aged postnatal day 4 (P4) to P18 were examined. This included recording action potential frequency, threshold, height and slope, and input resistance and capacitance. Changes in a number of these properties were observed, suggesting significant changes in voltage-gated Na(+) currents. Because voltage-gated Na(+) currents, including the transient, resurgent and persistent currents, are known to play important roles in generating spontaneous action potentials, the developmental changes in these currents were examined. A large increase in the density of transient current, resurgent current and persistent current was observed at times corresponding with changes in action potential properties. Interestingly, the developmental up-regulation of the persistent current and resurgent current occurred at rate which was faster than the up-regulation of the transient current. Moreover, the relative amplitudes of the persistent and resurgent currents increased in parallel, suggesting that they share a common basis. The data indicate that developmental up-regulation of Na(+) currents plays a key role in the acquisition of Purkinje neuron excitability.

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Year:  2006        PMID: 17100843     DOI: 10.1111/j.1460-9568.2006.05139.x

Source DB:  PubMed          Journal:  Eur J Neurosci        ISSN: 0953-816X            Impact factor:   3.386


  8 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2012-04-09       Impact factor: 11.205

4.  β-Site APP-cleaving enzyme 1 (BACE1) cleaves cerebellar Na+ channel β4-subunit and promotes Purkinje cell firing by slowing the decay of resurgent Na+ current.

Authors:  Tobias Huth; Andrea Rittger; Paul Saftig; Christian Alzheimer
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7.  Human Nav1.6 Channels Generate Larger Resurgent Currents than Human Nav1.1 Channels, but the Navβ4 Peptide Does Not Protect Either Isoform from Use-Dependent Reduction.

Authors:  Reesha R Patel; Cindy Barbosa; Yucheng Xiao; Theodore R Cummins
Journal:  PLoS One       Date:  2015-07-16       Impact factor: 3.240

8.  Infant and adult SCA13 mutations differentially affect Purkinje cell excitability, maturation, and viability in vivo.

Authors:  Jui-Yi Hsieh; Brittany N Ulrich; Fadi A Issa; Meng-Chin A Lin; Brandon Brown; Diane M Papazian
Journal:  Elife       Date:  2020-07-09       Impact factor: 8.140

  8 in total

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