Abstract

The absorbance change of the weak base dye probe, Acridine orange, was used to monitor alterations of pH gradients across renal brush border membrane vesicles. The presence of Na +/H + or Li +/H + exchange was demonstrated by diluting Na 2SO 4 or Li 2SO 4 loaded vesicles into Na +- or Li +-free solutions, which caused dye uptake. About 20% of the uptake was abolished by lipid permeable cations such as valinomycin-K + or tetraphenylphosphonium, indicating perhaps the presence of a finite Na + conductance smaller than electroneutral Na +/H + exchange. The protonophore tetrachlorosalicylanilide raised the rate of dye uptake under these conditions, hence the presence of an Na + conductance greater than the H + conductance was suggested. K + gradients also induced changes of pH, at about 10% of the Na + or Li + rate. Partial inhibition (21%) was seen with 0.1 mM amiloride indicating that K + was a low affinity substrate for the Na +/H + exchange. Acceleration both by tetrachlorosalicylanilide (2-fold) and valinomycin (4-fold) suggested the presence of 2 classes of vesicles, those with high and those with low K + conductance. The larger magnitude of the valinomycin dependent signal suggested that 75% of the vesicles had a low K + conductance. Inward Cl − gradients also induced acidification, partially inhibited by the presence of tetraphenylphosphonium, and accelerated by tetrachlorosalicylanilide. Thus both a Cl − conductance greater than the H + conductance and a Cl −/OH − exchange were present. The rate of Na +/H + exchange was amiloride sensitive with a pH optimum of 6.5 and an apparent K m for Na + or Li + of about 10 mM and an E A of 14.3 kcal per mol. A 61-fold Na 2SO 4 gradient resulted in a pH gradient of 1.64 units which increased to 1.8 with gramicidin. An equivalent NaCl gradient gave a much lower ΔpH even in the presence of gramicidin showing that the H + and Cl − pathways could alter the effects of the Na +/H + exchange.

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