Browsing by Author "Chang, Joshua"

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    Mutant SOD1 protein increases Na(v)1.3 channel excitability
    (SPRINGER, 2016-01-01) Oktem, Elif Kubat; Mruk, Karen; Chang, Joshua; Akin, Ata; Kobertz, William R.; Brown Jr., Robert H.
    Amyotrophic lateral sclerosis (ALS) is a lethal paralytic disease caused by the degeneration of motor neurons in the spinal cord, brain stem, and motor cortex. Mutations in the gene encoding copper/zinc superoxide dismutase (SOD1) are present in similar to 20\% of familial ALS and similar to 2\% of all ALS cases. The most common SOD1 gene mutation in North America is a missense mutation substituting valine for alanine (A4V). In this study, we analyze sodium channel currents in oocytes expressing either wild-type or mutant (A4V) SOD1 protein. We demonstrate that the A4V mutation confers a propensity to hyperexcitability on a voltage-dependent sodium channel (Na(v)1.3) mediated by heightened total Na+ conductance and a hyperpolarizing shift in the voltage dependence of Na(v)1.3 activation. To estimate the impact of these channel effects on excitability in an intact neuron, we simulated these changes in the program NEURON
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    Mutant SOD1 protein increases Na(v)1.3 channel excitability (vol 42, pg 351, 2016)
    (SPRINGER, 2016-01-01) Oktem, Elif Kubat; Mruk, Karen; Chang, Joshua; Akin, Ata; Kobertz, William R.; Brown Jr., Robert H.