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Nanosecond electric pulses differentially affect inward and outward currents in patch clamped adrenal chromaffin cells
Date
2017Type
ArticleAbstract
This study examined the effect of 5 ns electric pulses on macroscopic ionic currents in whole-cell voltage-clamped adrenal chromaffin cells. Current-voltage (I-V) relationships first established that the early peak inward current was primarily composed of a fast voltage-dependent Na+ current (I-Na), whereas the late outward current was composed of at least three ionic currents: a voltage-gated Ca2+ current (I-Ca), a Ca2+-activated K+ current (I-K(Ca)), and a sustained voltage-dependent delayed rectifier K+ current (I-KV). A constant-voltage step protocol was next used to monitor peak inward and late outward currents before and after cell exposure to a 5 ns pulse. A single pulse applied at an electric (E)-field amplitude of 5 MV/m resulted in an instantaneous decrease of similar to 4% in peak INa that then declined exponentially to a level that was similar to 85% of the initial level after 10 min. Increasing the E-field amplitude to 8 or 10 MV/m caused a twofold greater inhibitory effect on peak INa. The decrease in INa was not due to a change in either the steady-state inactivation or activation of the Na+ channel but instead was associated with a decrease in maximal Na+ conductance. Late outward current was not affected by a pulse applied at 5 MV/m. However, for a pulse applied at the higher E-field amplitudes of 8 and 10 MV/m, late outward current in some cells underwent a progressive similar to 22% decline over the course of the first 20 s following pulse exposure, with no further decline. The effect was most likely concentrated on ICa and IK(Ca) as IKV was not affected. The results of this study indicate that in whole-cell patch clamped adrenal chromaffin cells, a 5 ns pulse differentially inhibits specific voltage-gated ionic currents in a manner that can be manipulated by tuning E-field amplitude.
Permanent link
http://hdl.handle.net/11714/5441Additional Information
Journal Title | PLoS ONE |
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Rights | Creative Commons Attribution 4.0 International |
Rights Holder | Authors |