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Enhanced Monitoring of Nanosecond Electric Pulse-Evoked Membrane Conductance Changes in Whole-Cell Patch Clamp Experiments.
Yoon, Jihwan; Leblanc, Normand; Zaklit, Josette; Vernier, P Thomas; Chatterjee, Indira; Craviso, Gale L.
Afiliação
  • Yoon J; Department of Electrical and Biomedical Engineering, College of Engineering, University of Nevada, Reno, Reno, NV, 89557, USA.
  • Leblanc N; Department of Pharmacology, University of Nevada School of Medicine, Reno, NV, 89557, USA.
  • Zaklit J; Department of Electrical and Biomedical Engineering, College of Engineering, University of Nevada, Reno, Reno, NV, 89557, USA.
  • Vernier PT; Frank Reidy Research Center for Bioelectrics, Old Dominion University, Norfolk, VA, 23508, USA.
  • Chatterjee I; Department of Electrical and Biomedical Engineering, College of Engineering, University of Nevada, Reno, Reno, NV, 89557, USA.
  • Craviso GL; Department of Pharmacology, University of Nevada School of Medicine, Reno, NV, 89557, USA. gcraviso@medicine.nevada.edu.
J Membr Biol ; 249(5): 633-644, 2016 10.
Article em En | MEDLINE | ID: mdl-27075358
ABSTRACT
Patch clamp electrophysiology serves as a powerful method for studying changes in plasma membrane ion conductance induced by externally applied high-intensity nanosecond electric pulses (NEPs). This paper describes an enhanced monitoring technique that minimizes the length of time between pulse exposure and data recording in a patch-clamped excitable cell. Whole-cell membrane currents were continuously recorded up to 11 ms before and resumed 8 ms after delivery of a 5-ns, 6 MV/m pulse by a pair of tungsten rod electrodes to a patched adrenal chromaffin cell maintained at a holding potential of -70 mV. This timing was achieved by two sets of relay switches. One set was used to disconnect the patch pipette electrode from the pre-amplifier and connect it to a battery to maintain membrane potential at -70 mV, and also to disconnect the reference electrode from the amplifier. The other set was used to disconnect the electrodes from the pulse generator until the time of NEP/sham exposure. The sequence and timing of both sets of relays were computer-controlled. Using this procedure, we observed that a 5-ns pulse induced an instantaneous inward current that decayed exponentially over the course of several minutes, that a second pulse induced a similar response, and that the current was carried, at least in part, by Na+. This approach for characterizing ion conductance changes in an excitable cell in response to NEPs will yield information essential for assessing the potential use of NEP stimulation for therapeutic applications.
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Base de dados: MEDLINE Assunto principal: Técnicas de Patch-Clamp / Fenômenos Eletrofisiológicos / Potenciais da Membrana Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Técnicas de Patch-Clamp / Fenômenos Eletrofisiológicos / Potenciais da Membrana Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article