Changes in absorption, fluorescence, dichroism, and birefringence in stained giant axons: Optical measurement of membrane potential

1977 ◽  
Vol 33 (1) ◽  
pp. 141-183 ◽  
Author(s):  
W. N. Ross ◽  
B. M. Salzberg ◽  
L. B. Cohen ◽  
A. Grinvald ◽  
H. V. Davila ◽  
...  
Keyword(s):  
Membrane Potential ◽  
Optical Measurement ◽  
Giant Axons

Optical Measurement of Membrane Potential in Invertebrate Ganglia and Mammalian Cortex

1989 ◽  
pp. 329-346 ◽  
Author(s):  
JIAN-YOUNG WU ◽  
JILL A. LONDON ◽  
DEJAN ZECEVIC ◽  
LESLIE M. LOEW ◽  
HARRY S. ORBACH ◽  
...  
Keyword(s):  
Membrane Potential ◽  
Optical Measurement ◽  
Invertebrate Ganglia

Optical measurement of the plasma-membrane potential of mammalian cells grown in monolayer culture

1981 ◽  
Vol 9 (1) ◽  
pp. 80-81 ◽  
Author(s):  
C. LINDSAY BASHFORD ◽  
KEITH A. FOSTER ◽  
KINGSLEY J. MICKLEM ◽  
CHARLES A. PASTERNAK
Keyword(s):  
Plasma Membrane ◽  
Membrane Potential ◽  
Mammalian Cells ◽  
Monolayer Culture ◽  
Optical Measurement ◽  
Plasma Membrane Potential

scholarly journals Current- and Voltage-Clamped Studies on Myxicola Giant Axons

1969 ◽  
Vol 54 (6) ◽  
pp. 730-740 ◽  
Author(s):  
L. Binstock ◽  
L. Goldman
Keyword(s):  
Steady State ◽  
Membrane Potential ◽  
Action Potential ◽  
Voltage Clamp ◽  
Transient Current ◽  
Resting Membrane Potential ◽  
Action Potential Amplitude ◽  
Giant Axons ◽  
Potential Amplitude ◽  
Steady State Current

A new dissection procedure for preparing Myxicola giant axons for observation under voltage clamp is described. Preparation time is generally 40–45 min. 65–70% of the preparations attempted may be brought through the entire procedure, including insertion of the long internal electrode, and support an initial action potential amplitude of 100 mv or greater. Mean values for axon diameter, resting membrane potential, action potential amplitude, maximum peak inward transient current, and resting membrane resistance are 560 µ, —66.5 mv, 112 mv, 0.87 ma/cm2 and 1.22 KΩ cm 2 respectively. Cut branches do not seem to be a problem in this preparation. Behavior under voltage clamp is reasonably stable over several hours. Reductions in maximum inward transient current of 10% and in steady-state current of 5–10% are expected in the absence of any particular treatment. Tetrodotoxin blocks the action potential and both the inward and outward transient current, but has no effect on either the resting membrane potential or the steady-state current. This selective action of tetrodotoxin on the transient current is taken as an indication that this current component is probably carried by Na.

scholarly journals The influence of external cations and membrane potential on Ca-activated Na efflux in Myxicola giant axons.

1978 ◽  
Vol 71 (4) ◽  
pp. 453-466 ◽  
Author(s):  
R A Sjodin ◽  
R F Abercrombie
Keyword(s):  
Membrane Potential ◽  
Direct Action ◽  
Monovalent Cation ◽  
Coupling Ratio ◽  
Large Component ◽  
Experimental Conditions ◽  
Giant Axons ◽  
Threefold Increase ◽  
Na Efflux ◽  
External K

In microinjected Myxicola giant axons with elevated [Na]i, Na efflux was sensitive to Cao under some conditions. In Li seawater, sensitivity to Cao was high whereas in Na seawater, sensitivity to Cao was observed only upon elevation of [Ca]o above the normal value. In choline seawater, the sensitivity of Na efflux to Cao was less than that observed in Li seawater whereas Mg seawater failed to support any detectable Cao-sensitive Na efflux. Addition of Na to Li seawater was inhibitory to Cao-sensitive Na efflux, the extent of inhibition increasing with rising values of [Na]o. The presence of 20 mM K in Li seawater resulted in about a threefold increase in the Cao-activated Na efflux. Experiments in which the membrane potential, Vm, was varied or held constant when [K]o was changed showed that the augmentation of Ca-activated Na efflux by Ko was not due to changes in Vm but resulted from a direct action of K on activation by Ca. The same experimental conditions that favored a large component of Cao-activated Na efflux also caused a large increase in Ca influx. Measurements of Ca influx in the presence of 20 mM K and comparison with values of Ca-activated Na efflux suggest that the Na:Ca coupling ratio may be altered by increasing external [K]o. Overall, the results suggest that the Cao-activated Na efflux in Myxicola giant axons requires the presence of an external monovalent cation and that the order of effectiveness at a total monovalent cation concentration of 430 mM is K + Li greater than Li greater than Choline greater than Na.

scholarly journals Current Separations in Myxicola Giant Axons

1969 ◽  
Vol 54 (6) ◽  
pp. 741-754 ◽  
Author(s):  
L. Goldman ◽  
L. Binstock
Keyword(s):  
Membrane Potential ◽  
Action Potential ◽  
Reversal Potential ◽  
Transient Current ◽  
Resting Potential ◽  
Equilibrium Potential ◽  
Resting Membrane Potential ◽  
Concentration Data ◽  
Giant Axons ◽  
Current Reversal

The effect of reducing the external sodium concentration, [Na]o, on resting potential, action potential, membrane current, and transient current reversal potential in Myxicola giant axons was studied. Tris chloride was used as a substitute for NaCl. Preliminary experiments were carried out to insure that the effect of Tris substitution could be attributed entirely to the reduction in [Na]o. Both choline and tetramethylammonium chloride were found to have additional effects on the membrane. The transient current is carried largely by Na, while the delayed current seems to be independent of [Na]o. Transient current reversal potential behaves much like a pure Nernst equilibrium potential for sodium. Small deviations from this behavior are consistent with the possibility of some small nonsodium component in the transient current. An exact PNa/PK for the transient current channels could not be computed from these data, but is certainly well greater than unity and possibly quite large. The peak of the action potential varied with [Na]o as expected for a sodium action potential with some substantial potassium permeability at the time of peak. Resting membrane potential is independent of [Na]o. This finding is inconsistent with the view that the resting membrane potential is determined only by the distribution of K and Na, and PNa/PK. It is suggested that PNa/PK's obtained from resting membrane potential-potassium concentration data do not always have the physical meaning generally attributed to them.

scholarly journals Comparative study on neural oscillation in the procerebrum of the terrestrial slugs Incilaria bilineata and

1997 ◽  
Vol 200 (13) ◽  
pp. 1851-1861 ◽  
Author(s):  
S Kawahara ◽  
S Toda ◽  
Y Suzuki ◽  
S Watanabe ◽  
Y Kirino
Keyword(s):  
Membrane Potential ◽  
Electrical Properties ◽  
Optical Measurement ◽  
Cell Mass ◽  
Field Potential ◽  
Opposite Polarity ◽  
Oscillatory Activity ◽  
Internal Mass ◽  
Neural Oscillation ◽  
Limax Maximus

Coherent oscillatory activities in procerebral neurones have been described in Limax maximus; however, the electrical properties of the procerebrum of other terrestrial molluscs are less well understood. We have examined oscillatory activity in the procerebrum of Incilaria bilineata and Limax marginatus. The local field potential measured in the procerebrum of I. bilineata showed repetitive peaks which had the opposite polarity from those measured in L. marginatus. Optical measurement of membrane potential using a potential-sensitive dye, di-4-ANEPPS, showed that the oscillations in I. bilineata occurred mainly in the internal mass while those in L. marginatus were located in the cell mass. An analysis of the waveform revealed that the depolarizing phase of the oscillations consists of both a slow and a rapid component in both species. The rapid component was most pronounced in the internal mass of I. bilineata but was prominent in the cell mass of L. marginatus. The superior tentacle nerve, which projects to the terminal mass, also showed oscillations in synchrony with those of the procerebrum. These results suggest that oscillations in procerebral interneurones are commonly generated in a region adjacent to the terminal mass and that these oscillations may affect the membrane potential of the neurones constituting the superior tentacle nerve.

scholarly journals Leak Current Rectification in Myxicola Giant Axons

1969 ◽  
Vol 54 (6) ◽  
pp. 755-764 ◽  
Author(s):  
L. Goldman ◽  
L. Binstock
Keyword(s):  
Field Equation ◽  
Membrane Potential ◽  
Resting Membrane Potential ◽  
Constant Field ◽  
Leak Current ◽  
Giant Axons ◽  
Time To Peak ◽  
Zero Current ◽  
Current Voltage ◽  
Current Voltage Curve

Early leak current, i.e. for times similar to the time to peak of the transient current was measured in Myxicola giant axons in the presence of tetrodotoxin. The leak current-voltage relation rectifies, showing more current for strong depolarizing pulses than expected from symmetry around the holding potential. A satisfactory practical approximation for most leak corrections is constant resting conductance. The leak current-voltage curve rectifies less than expected from the constant field equation. These curves cannot be reconstructed by summing the constant field currents for sodium and potassium using a PNa/PK ratio obtained in the usual way, from zero current constant field fits to resting membrane potential data. Nor can they be reconstructed by summing the constant field current for potassium with that for any other single ion. They can be reconstructed, however, by summing the constant field current for potassium with a constant conductance component. It is concluded that the leak current and the resting membrane potential, therefore, are determined by multiple ionic components, at least three and possibly many. Arguments are presented suggesting that ion permeability ratios obtained in the usual way, by fitting the constant field equation to resting membrane potential data should be viewed with skepticism.

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