Na transport stimulation by novobiocin: intracellular ion concentrations and membrane potential.

Microelectrodes and electron microprobe analysis were employed to study the effect of novobiocin on membrane potential and intracellular electrolyte concentrations in the frog skin epithelium. In both species investigated (Rana esculenta and Rana temporaria), novobiocin (1 mM, outer bath) caused a stimulation of transepithelial Na transport, a depolarization of apical membrane potential, a fall in the apical fractional resistance, and an increase in the intracellular Na concentration. The rise in the Na concentration was accompanied by an equivalent fall in the K concentration. All effects of novobiocin were fully reversible by subsequent application of amiloride. The depolarization as well as the Na increase suggests that the natriferic effect of novobiocin is due to a stimulation of the apical Na influx. Combining both measurements it was possible to calculate the effect of novobiocin on the Na permeability of the apical membrane directly. In Rana esculenta novobiocin increased the permeability from 4.5 to 23.2 nm/s. In Rana temporaria the increase was significantly smaller, from 8.7 to 16.9 nm/s. The transport rate as measured by the short-circuit current showed a non-linear dependence on the apical Na permeability. In the range of transport rates normally encountered, however, the current was a linear function of the Na permeability consistent with the view that the apical membrane is rate-limiting in transepithelial Na transport.

Na transport stimulation by novobiocin: transepithelial parameters and evaluation of ENa.

The action of the antibiotic novobiocin on transepithelial Na transport was studied in isolated skins obtained from two different frog species. In Rana esculenta addition of novobiocin to the outer bath (1 mM) resulted in a sustained and reversible stimulation of the short-circuit current, transepithelial potential, and transepithelial conductance. Similar, though more variable and much less pronounced changes were observed in Rana temporaria. In the presence of amiloride (0.1 mM) novobiocin had no effect on any of the investigated transport parameters and all novobiocin induced changes were fully reversed when amiloride was given subsequently. At reduced external Na concentration or low pH the action of novobiocin was found to be greatly attenuated. In the presence of novobiocin an increased affinity to amiloride and a linearization of the transepithelial current-voltage relationship was observed. The results are consistent with the view that novobiocin increases the Na permeability of the outer membrane, possibly by an attenuation of an Na self-inhibition mechanism. In addition, the driving force of transepithelial Na transport was estimated by means of novobiocin. Several different methods were employed, providing varying results. As shown in an Appendix, for the most part the discrepancies can be explained by changes in the intracellular Na and K concentration. In some cases, novobiocin induced large secondary increases in the skin conductance which can be referred to an increased Cl permeability.