Transient Current Measurement

Transient current measurement is an electrophysiological method for recording brief changes in electrical current that occur when a biological membrane experiences a defined voltage or chemical stimulus. In patch-clamp or voltage-clamp experiments, the recording system applies a controlled voltage step and measures rapid capacitive currents and ion-channel currents as membrane charge redistributes and channels open, close, or inactivate. These measurements help characterize channel kinetics, membrane excitability, synaptic signaling, and transport processes in cells and tissues. By quantifying current amplitude, timing, and decay, researchers can link molecular channel behavior to physiological function and investigate how drugs, mutations, or disease alter cellular electrical activity.

Transient Current Measurement - Related Videos

Research

JoVE Journal - Biology
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Isolation of Human Atrial Myocytes for Simultaneous Measurements of Ca2+ Transients and Membrane Currents

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Cited by 29 •

2013

We describe the isolation of human atrial myocytes which can be used for intracellular Ca2+ measurements in combination with electrophysiological patch-clamp studies.

Research

JoVE Journal - Bioengineering

Measurement of Bioelectric Current with a Vibrating Probe

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Cited by 15 •

2011

The manufacture, calibration and use of non-invasive vibrating probes to measure bioelectric current in various biological systems is described.

Isolation of High Quality Murine Atrial and Ventricular Myocytes for Simultaneous Measurements of Ca2+ Transients and L-Type Calcium Current

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Cited by 3 •

2020

Mouse models allow studying key mechanisms of arrhythmogenesis. For this purpose, high quality cardiomyocytes are necessary to perform patch-clamp measurements. Here, a method to isolate murine atrial and ventricular myocytes via retrograde enzyme-based Langendorff perfusion, which allows simultaneous measurements of calcium-transients and L-type calcium current, is described.

Whole-Cell Recording of Calcium Release-Activated Calcium (CRAC) Currents in Human T Lymphocytes

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Cited by 5 •

2010

We provide a step-by-step protocol for whole-cell patch clamp recording of Calcium Release-Activated Calcium (CRAC) currents in peripheral blood mononuclear cell-derived human T lymphocytes.

Research

JoVE Journal - Biology
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Demonstration of Proteolytic Activation of the Epithelial Sodium Channel (ENaC) by Combining Current Measurements with Detection of Cleavage Fragments

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Cited by 4 •

2014

Proteolytic activation of the epithelial sodium channel (ENaC) heterologously expressed in Xenopus laevis oocytes can be demonstrated by combining current measurements with a biotinylation approach to investigate the appearance of ion channel cleavage products at the cell surface. Functionally important cleavage sites can be identified by using site-directed mutagenesis.

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