Nakagawa N, Ghishan F K
Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-2576.
Proc Soc Exp Biol Med. 1994 Feb;205(2):162-7. doi: 10.3181/00379727-205-43692.
Renal and jejunal absorption of inorganic phosphate (P(i)) increases with dietary P(i) 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-P(i) 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-P(i) 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-P(i) diet (0.035 vs 0.017) (P < 0.01). Kinetics of renal Na(+)-dependent phosphate uptake in Hyp mice showed a Vmax of 1.00 +/- 0.01 and 0.46 +/- 0.02 nmoles/mg protein/15 sec in low- and control-P(i) 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 Vmax of 2.4 +/- 0.17 and 1.18 +/- 0.09 (P < 0.01) and Km of 0.07 +/- 0.03 and 0.08 +/- 0.03 on low and control P(i) diets, respectively. Similarly, low-P(i) 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-P(i) diet, respectively. Kinetic analysis in jejunal BBM of normal mice showed a Vmax 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-P(i) diets, respectively. The data indicates that low-phosphate diet upregulates the Vmax of the renal and jejunal Na(+)-dependent phosphate cotransporter in the hypophosphatemic mice.
在大鼠中,肾脏和空肠对无机磷酸盐(P(i))的吸收会随着饮食中P(i)限制而增加。钠依赖性磷酸盐转运体的缺陷已定位到Hyp小鼠的肾脏;然而,Hyp小鼠肾脏和空肠对低磷饮食的适应性尚未得到充分表征。因此,当前的研究旨在表征Hyp小鼠肾脏和空肠中钠依赖性磷酸盐转运的适应性,并将其与正常小鼠进行比较。与对照磷饮食喂养的小鼠相比,低磷饮食显著增加了肾脏刷状缘膜(BBM)磷酸盐摄取初始速率的斜率(0.035对0.017)(P < 0.01)。Hyp小鼠肾脏中钠依赖性磷酸盐摄取的动力学显示,在低磷和对照磷饮食中,Vmax分别为1.00±0.01和0.46±0.02纳摩尔/毫克蛋白质/15秒(P < 0.01),而Km值分别为0.07±0.04和0.02±0.01。正常小鼠肾脏BBM的类似动力学分析显示,在低磷和对照磷饮食中,Vmax分别为2.4±0.17和1.18±0.09(P < 0.01),Km分别为0.07±0.03和0.08±0.03。同样,低磷饮食显著增加了肠道磷酸盐摄取初始速率的斜率(0.013和0.007)(P < 0.01)。Hyp小鼠空肠中钠依赖性磷酸盐摄取的动力学显示,在低磷和对照磷饮食中,Vmax分别为0.36±0.01和0.2±0.02纳摩尔/毫克蛋白质/15秒(P < 0.01),Km分别为0.13±0.06和0.06±0.01毫摩尔。正常小鼠空肠BBM的动力学分析显示,在低磷和对照磷饮食中,Vmax分别为0.47±0.04和0.18±0.01纳摩尔/毫克蛋白质/15秒(P < 0.01),Km分别为0.16±0.04和0.11±0.01。数据表明,低磷饮食上调了低磷血症小鼠肾脏和空肠中钠依赖性磷酸盐共转运体的Vmax。