Nanosecond pulse electric field (nanopulse): a novel non-ligand agonist for platelet activation.

Abstract

Nanosecond pulse stimulation of a variety of cells produces a wide range of physiological responses (e.g., apoptosis, stimulation of calcium (Ca2+) fluxes, changes in membrane potential). In this study, we investigated the effect of nanosecond pulses, which generate intense electric fields (nsPEFs), on human platelet aggregation, intracellular free Ca2+ ion concentration ([Ca2+]i) and platelet-derived growth factor release. When platelet rich plasma was pulsed with one 300ns pulse with an electric field of 30kV/cm, platelets aggregated and a platelet gel was produced. Platelet aggregation was observed with pulses as low as 7kV/cm with maximum effects seen with approximately 30kV/cm. The increases in intracellular Ca2+ release and Ca2+ influx were dose dependent on the electrical energy density and were maximally stimulated with approximately 30kV/cm. The increases in [Ca2+]i induced by nsPEF were similar to those seen with thapsigargin but not thrombin. We postulate that nsPEF caused Ca2+ to leak out of intracellular Ca2+ stores by a process involving the formation of nanopores in organelle membranes and also caused Ca2+ influx through plasma membrane nanopores. We conclude that nsPEFs dose-dependently cause platelets to rapidly aggregate, like other platelet agonists, and this is most likely initiated by the nsPEFs increasing [Ca2+]i, however by a different mechanism.

DOI: 10.1016/j.abb.2007.12.009
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@article{Zhang2008NanosecondPE, title={Nanosecond pulse electric field (nanopulse): a novel non-ligand agonist for platelet activation.}, author={Jue Zhang and Peter F. Blackmore and Barbara Y. Hargrave and Shu Xiao and Stephen J. Beebe and Karl H. Schoenbach}, journal={Archives of biochemistry and biophysics}, year={2008}, volume={471 2}, pages={240-8} }