The effect of ultraviolet light on the sodium and potassium composition of resting yeast cells

The Na⁺ and K⁺ content of non-metabolizing yeast cells was determined before and after monochromatic ultraviolet (UV) irradiation. UV facilitated the uptake of Na⁺ into and the loss of K⁺ from the cells (net ion flux); the effect is greatest for the shortest wavelength employed (239 mµ) and is partly dependent upon the presence of oxygen. The UV effect on net ion flux persists for at least 90 minutes during which tests were made and it occurs following dosages which are without measurable effect on colony formation. The UV effect on net ion flux is decreased by acidity and promoted by alkalinity. Addition of calcium ions in sufficient amount prevents the usual net ion flux changes observed in irradiated yeast. Increase in concentration gradient between the inside and the outside of the cell increases the net ion flux of irradiated yeast, Na⁺ uptake leading K⁺ loss in all cases. UV appears to act by disorganizing the constituents of the cell surface, permitting K⁺ to leave the cell in exchange for Na⁺. At low intensities of UV this ionic exchange approaches equivalence, but at higher intensities more Na⁺ is taken up than K⁺ is lost. Some evidence suggests that the Na⁺ in excess over that exchanged for K⁺ is adsorbed to charged groups produced by the photochemical effect of UV on the cell surface.     

Strophanthidin-sensitive components of potassium and sodium movements in skeletal muscle as influenced by the internal sodium concentration

"Low sodium" muscles were prepared which contained around 5 mmoles/kg fiber of intracellular sodium. "High sodium" muscles containing between 15 and 30 mmoles/kg fiber of intracellular sodium were also prepared. In low sodium muscles application of 10^-5 M strophanthidin reduced potassium influx by about 5%. Potassium efflux was unaffected by strophanthidin under these conditions. In high sodium muscles, 10^-5 M strophanthidin reduced potassium influx by 45% and increased potassium efflux by 70%, on the average. In low sodium muscles sodium efflux was reduced by 25% during application of 10^-5 M strophanthidin while in high sodium muscles similarly treated, sodium efflux was reduced by about 60%. Low sodium muscles showed a large reduction in sodium efflux when sodium ions in the Ringer solution were replaced by lithium ions. The average reduction in sodium efflux was 4.5-fold. Of the amount of sodium efflux remaining in lithium. Ringer''s solution, 40% could be inhibited by application of 10^-5 M strophanthidin. The total sodium efflux from low sodium muscles exposed to Ringer''s solution in which lithium had been substituted for sodium ions for a period of 1 hr can be fractionated as 78% Na-for-Na interchange, 10% strophanthidin-sensitive sodium pump, and 12% residual sodium efflux. It is concluded that large strophanthidin-sensitive components of sodium and potassium flux can be expected only at elevated sodium concentrations within the muscle cells.     

The influence of ionic strength on potassium contractures and calcium movements in frog muscle

Frog toe muscles were bathed in isotonic, sodium-free Tris chloride, methanesulfonate, or sulfate solutions containing sucrose or mannitol and varying in ionic strength from 0.006 to 0.291. By decreasing the ionic strength the curve relating the peak tension of the K contractures to the log [K] was reversibly shifted to lower [K]. Increasing the [Ca] from 1 to 4 mM almost abolished this effect. The resting uptake of ⁴⁵Ca was increased more than two times by decreasing the ionic strength from 0.125 to 0.039. It was not increased significantly by raising [Ca] from 1 to 4 mM at low or normal ionic strength. The additional uptake of ⁴⁵Ca during contractures provoked by 120 mM K was not significantly different at the two levels of ionic strength. The rate of emergence of ⁴⁵Ca from muscles loaded with ⁴⁵Ca at reduced ionic strength, was decreased. The effects of low ionic strength are discussed in terms of changes in the potential difference across a membrane with fixed negative charges on the outer surface.     

The effect of certain anions on muscle resting potential in Tenebrio molitor

Experiments were carried out on longitudinal ventral muscles of the mealworm larva (Tenebrio molitor) using conventional microelectrode methods. Both sodium nitrate and sodium sulphate depolarized the fibres markedly, whereas sodium propionate exerted an hyperpolarizing influence. It is concluded that the differences in the mode of action are due to different permeabilities of the membrane to the applied anions. The results obtained confirm also the concept of a multi-ionic electrode with respect to insect muscle fibres.     

The effect of phloretin on single potassium channels in myelinated nerve

The effect of phloretin, a dipolar organic compound, on single potassium channel currents of myelinateed nerve fibres of Xenopus laevis has been investigated, using inside-out patches prepared by the method of Jonas et al. (1989). The I channel, a potential dependent K channel with intermediate deactivation kinetics, was reversibly blocked by 20 µM phloretin applied on the inside; the block was strongest at negative membrane potentials and less pronounced at positive potentials. Phloretin shifted the curve relating open probability to membrane potential towards more positive potentials and reduced its slope and maximum. This confirms previous findings on the effect of phloretin on the voltage dependence of the fast macroscopic K conductance. Single channel conductance and deactivation kinetics were not altered by phloretin. Offprint requests to: Correspondence to: H. Meves