Dietary K1 restriction upregulates total and Sch-28080-sensitive bicarbonate absorption in rat tIMCD

Wall, Susan M., Pramod Mehta, and Thomas D. DuBose, Jr. Dietary K1 restriction upregulates total and Sch28080-sensitive bicarbonate absorption in rat tIMCD. Am. J. Physiol. 275 (Renal Physiol. 44): F543–F549, 1998.—In tubules from the terminal segment of the inner medullary collecting duct (tIMCD) from rats with chronic metabolic acidosis, our laboratory has shown that bicarbonate absorption (JtCO2) is inhibited by removal of K1 from the luminal fluid or by the addition of Sch-28080 to the perfusate. The present study asked whether total and/or Sch-28080-sensitive JtCO2 is regulated by changes in systemic K1 homeostasis. Rat tIMCD tubules were perfused in vitro in symmetrical, HCO3 /CO2-buffered solutions containing 10 mM KCl 1 6 mM NH4Cl. Total and Sch-28080-sensitive JtCO2 were measured in rats with varying K1 intake. In K1-replete rats, baseline JtCO2 was 2.1 6 0.3 pmol ·mm21 ·min21 (n 5 6). In rats fed a K1-deficient diet for 3 days, JtCO2 was 5.4 6 0.7 pmol ·mm21 ·min21 (n 5 16, P , 0.05). To determine the mechanism for the increase in HCO3 2 absorption observed with K1 restriction, the Sch-28080-sensitive component of JtCO2 was measured in each treatment group. Following the addition of Sch-28080 (10 μM) to the perfusate, a 40% reduction in JtCO2 was observed in K1-restricted rats. JtCO2 was not reduced following the addition of Sch-28080 in rats with normal K1 intake. Because Sch-28080-sensitive JtCO2 was increased in K1-restricted rats, Sch-28080-sensitive JtCO2 was studied further in tIMCD tubules from rats in this treatment group. In K1-restricted rats, JtCO2 decreased by 20% following the addition of 5 mM ouabain to the perfusate. This ouabain-induced decline in JtCO2 was observed both in the presence and in the absence of Sch-28080. We conclude that total and Sch-28080-sensitive net acid secretion is increased with dietary K1 restriction. However, since ,50% of JtCO2 is insensitive to both Sch-28080 and ouabain, future studies will be necessary to define other mechanisms of luminal acidification in the rat tIMCD.