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Sodium transport in cultured rat renal papillary collecting tubule

Conference · · Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States)
OSTI ID:5389618
The renal papillary collecting duct (PCD) is the final site for regulation of sodium excretion. Cultured rat RPCT cells were investigated as a model for the PCD. Sodium transport was studied using /sup 22/Na/sup +/ uptake measurements. Steady state Na/sup +/ uptake was measured at 23/sup 0/C in the absence of K/sup +/ and in the presence of 0.1 mM ouabain. /sup 22/Na/sup +/ uptake by the monolayer (157 +/- 9 nmol/lg protein/3 min) was saturable at 100 mM extracellular NaCl and half-maximal uptake occurred at 40 mM NaCl. The sigmoidal velocity curve suggested more than one external binding site for Na/sup +/ as the Hill coefficient was 2. The measured uptake of /sup 22/Na/sup +/ appeared to be intracellular and was regulated by Na/sup +//K/sup +/ ATPase activity, since activation of the Na/sup +//K/sup +/ pump with K/sup +/, reduced /sup 22/Na/sup +/ accumulation seven-fold. The time course for uptake was linear, showed only a single component, and followed first order kinetics with a t/sub 1/2/ of 17 min. Amiloride inhibited /sup 22/Na/sup +/ uptake. A Dixon plot revealed a linear, mixed type of inhibition with a K/sub i/ of 16 ..mu..M amiloride. Over 70% inhibition of total uptake was observed at 0.1 mM amiloride. Lithium was an effective blocker of /sup 22/Na/sup +/ uptake. Chloride replacement uptake by only 20%. These results suggest that sodium uptake by cultured RPCT cells occurs via a saturable, amiloride-inhibitable channel. A Na/sup +/-Cl/sup -/, or a Na/sup +/-K/sup +/-Cl/sup -/ cotransport system does not appear as a major pathway.
Research Organization:
Case Western Reserve Univ., Cleveland, OH
OSTI ID:
5389618
Report Number(s):
CONF-8604222-
Conference Information:
Journal Name: Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States) Journal Volume: 45:3
Country of Publication:
United States
Language:
English

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