Action potential opens access for the charged cofactor to the chloroplasts of Chara corallina cells

2008 ◽  
Vol 55 (2) ◽  
pp. 175-184 ◽  
Author(s):  
A. A. Bulychev ◽  
N. A. Krupenina

The action potential in the cells of the freshwater alga Chara corallina is slower than that in the nerve by about 1000-fold. The depolarization phase is brought on by the outflow of the Cl - ions. Voltage-clamp studies show that this Cl - current can be described by the Hodgkin-Huxley equations for the Na+ transient in the squid axon. The only change necessary to the form of the Hodgkin-Huxley equations is an introduction of a time delay between the stimulus and the onset of excitation. This mathematical model of the Chara action potential facilitates a quantitative description of the effects of pH and temperature. While a pH shift alters various Hodgkin-Huxley parameters, temperature change influences mainly the activation and inactivation time constants but leaves the voltage-dependence of these parameters unaffected. The delays in excitation are both temperature and potential dependent. In future some corrections to the Hodgkin-Huxley picture of the Chara action potential may be necessary, as recent impedance measurements suggest a change in the membrane capacitance at the time of excitation.


1976 ◽  
Vol 3 (3) ◽  
pp. 275 ◽  
Author(s):  
MJ Beilby ◽  
HGJ Coster

An investigation has been made of the effect of temperature on excitation in cells of C. corallina. It was found that the duration both of the action potential and of the transient current during excitation under voltage clamp increased with decreasing temperature, from ~1 s at 40°C to ~30 s at 3.5°C. The form of the transient response, however, was independent of temperature. While the peak potential during an action potential was largely independent of temperature, the peak transient current during a voltage clamp increased with increasing temperature up to ~30°C. Beyond this temperature, the peak current decreased again with increasing temperature. The activation enthalphy (ΔH*) calculated from Arrhenius plots of the duration of the action potential or of the transient current under voltage clamp varied continuously with temperature, having the values of ~7 kJ/mol for T > 20°C and ~350 kJ/mol for T < 7°C. The peak of the transient conductance changes (during voltage clamp at -45 mV) increased progressively with increasing temperatures; for T < 7°C there was almost no transient change in conductance. °H* for peak transient conductance change was ~7 kJ/mol for T > 20°C and ~145 kJ/mol for T < 7°C. At low temperatures (<7°C), ΔH* for the excitation channels was similar to that for the dehydration of K+, Na+ or Cl- ions. At high temperatures (>35°C), ΔH* for both the passive and excitation channels was about the same as that for diffusion in a free solution. This suggests a progressive change in the degree of dehydration required for ion permeation in the channels. In the light of the known frequency dependence of the membrane capacitance of this species (at low frequencies), considerations are also given to the implications of the similarity in their temperature dependence, of the duration of the action potential and the duration of the transient currents during voltage clamps.


1979 ◽  
Vol 6 (3) ◽  
pp. 337 ◽  
Author(s):  
M.J Beilby ◽  
H.G.L Coster

An analysis, based on the Hodgkin-Huxley (H-H) equations is given of excitation processes in the plasmalemma of cells of C. corallina. Voltage clamp data for the plasmalemma show the presence of two activation and two inactivation processes and both of these transients are modelled in a manner analagous to the gated Na+ current in squid axons. Separation of the various ionic components of the experimental clamp currents was achieved by fitting the experimental data over a wide range of potentials to the model equations. The potential dependencies of the various H-H parameters for C. corallina, determined from the analysis of experimental results, are presented. A reconstruction is also given of the action potential and it is shown to be in satisfactory agreement with the experimental data. Comparisons are made of the experimental and predicted threshold potential, refractory period and the effects of the external Cl- and Ca�+ ion concentrations on the action potential. From the H-H parameters, the time courses during an action potential of the conductances g*Cl, g*x (� g*Ca?), the non activated/inactivated steady-state conductance g*ss, and the corresponding ionic currents I*Cl, I*x (� I*Ca?) and I*ss are calculated. While in the H-H analysis the peak value of g*x is found to be very large (larger than the peak value of g*Cl), it is shown that nevertheless I*Cl and I*ss dominate during an action potential.


1976 ◽  
Vol 3 (5) ◽  
pp. 687
Author(s):  
C.J Doughty ◽  
A.B Hope

When cells of C. corallina were irradiated with 254 nm ultraviolet light, the action potential across the plasmalemma was unaffected in its peak height, but its duration (measured at half-peak height) was increased, more so as the dose was varied between 1500 and 6000 J m-2. The action potential across the tonoplast was reduced in peak height and increased in duration by U.V. The effects were slowly reversible. The effect of 285 nm u.v., effective in depolarizing the resting potential difference, was to decrease the peak of the plasmalemma action potential while leaving the duration virtually unaffected. The results are interpreted as revealing differential effects on gating mechanisms determining the duration, and on transient membrane permeability to chloride (and possibly potassium) determining the peak, of the action potential. Because of the differential wavelength effects, these two membrane properties are postulated to be mediated by molecules which act as distinctive targets to the two wavelengths.


1994 ◽  
Vol 66 (5) ◽  
pp. 1694-1696 ◽  
Author(s):  
Z. Trontelj ◽  
R. Zorec ◽  
V. Jazbinsek ◽  
S.N. Erné

Author(s):  
Joachim R. Sommer ◽  
Teresa High ◽  
Betty Scherer ◽  
Isaiah Taylor ◽  
Rashid Nassar

We have developed a model that allows the quick-freezing at known time intervals following electrical field stimulation of a single, intact frog skeletal muscle fiber isolated by sharp dissection. The preparation is used for studying high resolution morphology by freeze-substitution and freeze-fracture and for electron probe x-ray microanlysis of sudden calcium displacement from intracellular stores in freeze-dried cryosections, all in the same fiber. We now show the feasibility and instrumentation of new methodology for stimulating a single, intact skeletal muscle fiber at a point resulting in the propagation of an action potential, followed by quick-freezing with sub-millisecond temporal resolution after electrical stimulation, followed by multiple sampling of the frozen muscle fiber for freeze-substitution, freeze-fracture (not shown) and cryosectionmg. This model, at once serving as its own control and obviating consideration of variances between different fibers, frogs etc., is useful to investigate structural and topochemical alterations occurring in the wake of an action potential.


Sign in / Sign up

Export Citation Format

Share Document