Proton permeability and the regulation of potassium permeability in mitochondria by uncoupling agents.

The addition of agents that uncouple electron transfer from energy conservation (uncouplers) to state 4 mitochondria causes the following ion movements: K(+) is extruded from the mitochondria in association with phosphate and possibly other anions, but not H(+). Endogenous Ca(++) is extruded from the mitochondria, and H(+) moves in to counter-balance the Ca(++) movement; some phosphate movement may be associated with Ca(++) extrusion. The rate and extent of K(+) extrusion induced by uncoupler is dependent on the concentrations of external phosphate and divalent ions. Phosphate induces K(+) extrusion, while Mg(++) and Mn(++) inhibit it. TheV max of K(+) transport is 300 μmoles K(+)/g protein per min. The K m for FCCP-induced potassium extrusion is 0.25 μM at pH 7.4. The inhibitory effect of Mg(++) is noncompetitive with respect to uncoupler concentration but competitive with respect to phosphate concentration. The experimental evidence does not support the existence of high H(+) permeability in the presence of uncoupler. A correlation is observed between the rate of K(+) extrusion and the energy reserves supplied from the high energy intermediate. The action of uncoupler in inducing K(+) permeability is considered to arise through its action in depleting the energy reserves of mitochondria rather than through a specific activating effect of permeability by the uncoupler itself. The relationship of membrane potential to regulation of K(+) permeability is discussed.