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CELLULAR CARDIAC ELECTROPHYSIOLOGICAL TECHNIQUES. NORBERT JOST, PhD. Electrical model of the membrane Standard intracellular microelectrode technique Voltage clamp technique Patch clamp technique. G=1/R. Ohm’s law. Ion channel model. Current clamp. Voltage clamp.
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CELLULAR CARDIAC ELECTROPHYSIOLOGICAL TECHNIQUES NORBERT JOST, PhD
Electrical model of the membrane Standard intracellular microelectrode technique Voltage clamp technique Patch clamp technique
Ohm’s law Ion channel model
Current clamp Voltage clamp
Intracellular microelectrode technique Re<< Rin Rin = 1012 Ohm
Ag/AgCl 3 M KCl Re ~ 10 - 40 MOhm 0.1 - 0.2 m
The setup amplifier computer ingerlő A/D d e r Detected signal P 0mV Organ bath d: stimulating electrode 50 mV e: microelectrode r: referent electrode 100 ms P: preparation
20 mV 100 ms 0 mV 50% APA Vmax 90% RP APD50 APD90 Pre-incubation drug Wash-out 60 min 20-60 min 60 min
Two microelectrode voltage clamp test potential voltage command holding potential The macroscopic sodium current
The voltage-clamp circuit follow up amplifier voltage measure voltage command amplifier Current measure
Patch-clamp: the special case of the voltage clamp (1) Suck a small piece of membrane onto the tip of a glass micropipette (~ 1 µm in diameter) Cell
Patch-clamp: the special case of the voltage clamp (2) “Gigaohm-seal” R > 1 GOhm Cell
Patch-clamp: the special case of the voltage clamp (3) Sense voltage here, inside the electrode, and use voltage clamp to keep it constant. Cell
Patch-clamp: the special case of the voltage clamp (3) Sense voltage here, inside the electrode, and use voltage clamp to keep it constant. closed open + + Cell
Patch-clamp: the special case of the voltage clamp (3) Turn on the aimed potential the inside part of the pipette and keep it constantly by applying the voltage clamp technique. closed open open Cell
Properties of individual voltage-dependent sodium channels voltage command 10 msec
Properties of individual voltage-dependent sodium channels • Individual channels are either open or closed (no partial openings)
Properties of individual voltage-dependent sodium channels • Individual channels are either open or closed (no partial openings) • Each channel opening is only a brief event compared to the total duration of the whole cell voltage-dependent sodium current. The macroscopic sodium current
Properties of individual voltage-dependent sodium channels • Individual channels are either open or closed (no partial openings) • Each channel opening is only a brief event compared to the total duration of the whole cell voltage-dependent sodium current. • Channel opening and closing is variable in duration and latency. The macroscopic sodium current
Properties of individual voltage-dependent sodium channels • The channels are either in open or closed state. • The channel openings are short events when compared with the macroscopic sodium current. • The time duration and latency of the channel openings are variable (case sensitive). Might happen to not open at all. • The open probability of the channels resembles with that of the macroscopic current. Summation of 300 recordings The macroscopic sodium current
Properties of individual voltage-dependent sodium channels • Individual channels are either open or closed (no partial openings) • Each channel opening is only a brief event compared to the total duration of the whole cell voltage-dependent sodium current. • Channel opening and closing is variable in duration and latency. • The overall probability of channel opening is similar to the total sodium current. Look at the sum of the currents from 300 trials. • Sometimes an individual channel doesn’t open even once. Summation of 300 recordings The macroscopic sodium current
Properties of individual voltage-dependent sodium channels • Individual channels are either open or closed (no partial openings) • Each channel opening is only a brief event compared to the total duration of the whole cell voltage-dependent sodium current. • Channel opening and closing is variable in duration and latency. • The overall probability of channel opening is similar to the total sodium current. Look at the sum of the currents from 300 trials. • Sometimes an individual channel doesn’t open even once. • Second openings are rare (because of inactivation) Summation of 300 recordings The macroscopic sodium current
Similarly, individual potassium channels, calcium channels, and other channels can be studied by patch clamping • Individual channels are either open or closed (no partial openings). Sometimes more than one channel is in a patch. • Each channel opening is only a brief event compared to the total duration of the whole cell current. • Channel opening and closing is variable in duration and latency. • The overall probability of channel opening is similar to the whole cell current • Second openings can happen if there’s no inactivation. Slowly inactivating K current channel (Ram & Dagan, 1987)
The configurations of the patch-clamp technique On-Cell Cell-Attached
The configurations of the patch-clamp technique Inside-out patch On-Cell
The configurations of the patch-clamp technique On-Cell Whole Cell
The configurations of the patch-clamp technique outside-out patch Whole Cell
The whole-cell configuration Rs Cm Rc
Extracellular solution (mM) (for K currents) Intracellukar solution (mM) (for K currents) NaCl 144 NaH2PO4 0.4 KCl 4 MgSO4 0.53 CaCl2 1.8 Glucose 5.5 HEPES 5 + ICa blocker K-aspartate 100 KCl 25 K2HPO4 10, K2EGTA 5 K2ATP 3 MgCl2 1 HEPES 10
The whole cell configuration Intracellular solution Patch-clamp amplifier Micropipette IBM PC + _ _ + _ + Extracellular solution _ _ + + + _ Cell _ + + _ + + _ _ 10 ms ... 5000 ms -20 mV ... +50 mV -40 mV
The “run-down“ effect The ATP-sensitive potassium current
The “run-down“ The L-type calcium current
The configurations of the patch clamp technique Whole Cell, perforated patch Whole Cell - amphotericin-B - nystatin
The “run-down” The L-type calcium current
Cell isolation - Ca2+ - free perfusion - enzymatic digestion (collagenase) - mechanical separation