Summary
Intracellular Pb2+ ions can replace Ca2+ ions in stimulating the Ca-dependent K permeability of human red blood cells. In metabolically depleted resealed ghosts, the threshold for stimulation of86Rb efflux by internal Pb2+ is around 5×10−10 m, and stimulation is half-maximal at about 2×10−9 m, and maximal at 10−8 m Pb2+. There is no effect on22Na efflux in this concentration range.86Rb efflux is antagonized by internal Mg2+ ions, and by the channel-blocking drugs quinidine and diS-C2(5), as observed for the Ca-dependent K permeability in red cells. In ghosts containing EDTA, which prevents any internal effects of Pb2+ ions, external Pb2+ increases both22Na and86Rb permeability when its concentration exceeds 6×10−7 m. This effect is seemingly unrelated to the Ca-dependent K permeability. This work makes extensive use of Pb2+ ion buffers, and gives information about their preparation and properties.
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Simons, T.J.B. Influence of lead ions on cation permeability in human red cell ghosts. J. Membrain Biol. 84, 61–71 (1985). https://doi.org/10.1007/BF01871648
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DOI: https://doi.org/10.1007/BF01871648