Renal and jejunal absorption of inorganic phosphate (P1) increases with dietary P1 restriction in the rat. The defect in Na+-dependent phosphate transporter has been localized to the kidney of the Hyp mice; however, the adaptation to low-P1 diet in both kidney and jejunum of the Hyp mice has not been well characterized. Therefore, the current studies were designed to characterize the adaptation of renal and jejunal Na+-dependent phosphate transport in the Hyp mice and compare it with normal mice. Low-P1 diet significantly increased the slope of the initial rate of renal brush border membrane (BBM) phosphate uptake compared with corresponding values in mice raised on control-P1 diet (0.035 vs 0.017) (P < 0.01). Kinetics of renal Na+-dependent phosphate uptake in Hyp mice showed a V max of 1.00 ± 0.01 and 0.46 ± 0.02 nmoles/mg protein/15 sec in low- and control-P1 diets, respectively (P < 0.01), whereas, Km values were 0.07 ± 0.04 and 0.02 ± 0.01, respectively. Similar kinetic analysis in renal BBM of normal mice showed a V max of 2.4 ± 0.17 and 1.18 ± 0.09 (P < 0.01) and K m of 0.07 ± 0.03 and 0.08 ± 0.03 on low and control P1 diets, respectively. Similarly, low-P1 diet significantly increased the slope of the initial rate of intestinal phosphate uptake (0.013 and 0.007) (P < 0.01). Kinetics of jejunal Na+-dependent phosphate uptake in Hyp mice showed a Vmax of 0.36 ± 0.01 and 0.2 ± 0.02 nmoles/mg protein/15 sec, (P < 0.01) and Km of 0.13 ± 0.06 and 0.06 ± 0.01 mM in low- and in control-P1 diet, respectively. Kinetic analysis in jejunal BBM of normal mice showed a V max of 0.47 ± 0.04 and 0.18 ± 0.01 nmoles/mg protein/15 sec (P < 0.01) and Km of 0.16 ± 0.04 and 0.11 ± 0.01 in low- and control-P1 diets, respectively. The data indicates that low-phosphate diet upregulates the V max of the renal and jejunal Na+-dependent phosphate cotransporter in the hypophosphatemic mice.
|Original language||English (US)|
|Number of pages||6|
|Journal||Proceedings of the Society for Experimental Biology and Medicine|
|State||Published - Feb 1994|
ASJC Scopus subject areas
- Biochemistry, Genetics and Molecular Biology(all)