Effects of a switched, time‐varying 1.7 T magnetic field on Rb+(K+) uptake by HeLa S3 cells incubated in an isosmotic high K+ medium were examined. The magnetic flux density was varied intermittently from 0.07–1.7 T at an interval of 3 s. K+ uptake was activated by replacement of normal medium by high K+ medium. A membrane‐permeable Ca2+ chelating agent (BAPTA‐AM) and Ca2+‐de pendent K+ channel inhibitors (quinine, charibdotoxin, and iberiotoxin) were found to reduce the Rb+(K+ ) uptake by about 30–40%. Uptake of K+ that is sensitive to these drugs is possibly mediated by Ca2+‐dependent K+ channels. The intermittent magnetic field partly suppress ed the drug‐sensitive K+ uptake by about 30–40% (P < 0.05). To test the mechanism of inhibition by the magnetic fields, intracellular Ca2+ concentration ([Ca2+]c) was measured using Fura 2‐AM. When cells were placed in the high K+ ; medium, [Ca2+]c increased to about 1.4 times the original level, but exposure to the magnetic fields completely suppressed the increase (P < 0.01). Addition of a Ca2+ ionophore (ionomycin) to the high K+ medium increased [Ca2+]c to the level of control cells, regardless of exposure to the magnetic field. But the inhibition of K+ uptake by the magnetic fields was not restored by addition of ionomycin. Based on our previous results on magnetic field‐induced changes in properties of the cell membrane, these results indicate that exposure to the magnetic fields partly suppresses K+ influx, which may be mediated by Ca2+‐dependent K+ channels. The suppress ion of K+ fluxes could relate to a change in electric properties of cell surface and an inhibition of Ca2+ influx mediated by Ca2+ channels of either the cell plasma membrane or the inner vesicular membrane of intracellular Ca2+ stores. Bioelectromagnetics 21:228–237, 2000. © 2000 Wiley‐Liss, Inc.