Glorieux F H, Morin C L, Travers R, Delvin E E, Poirier R
Pediatr Res. 1976 Jul;10(7):691-6. doi: 10.1203/00006450-197607000-00012.
The present report outlines an attempt to characterize inorganic phosphate uptake by human jejunal mucosa using biopsy material obtained from six patients affected by the X-linked form of vitamin D-resistant rickets and six control subjects. The tissue from control subjects accumulated 32P actively in a linear fashion against time. The incorporation of inorganic phosphate into organophosphate derivatives is rapid and equilibrates after 10 min at an inorganic over total phosphate ratio of 0.45. Concentrative uptake and incorporation were both suppressed by anaerobiosis or cyanide. Rates of phosphate uptake and incorporation into the organic derivatives by the tissue of hypophosphatemic patients are comparable with normal values. Saturation kinetics observed over a wide range of substrate concentrations (0.003 to 3 mM) elicits only one transport system with an apparent Michaelis constant of 0.2 mM and a maximum velocity of 0.7 mmol/liter/40 min. The kinetic data obtained from the patients do not strikingly differ from the control values. The chemical analysis of the phosphate content of intestinal mucosa from two patients and two control subjects indicates that the tissue is not specifically phosphate-depleted in the mutant individuals. These results are in accordance with the positive results obtained with the oral replacement therapy in familial hypophosphatemia.
本报告概述了一项利用从六名患有X连锁型维生素D抵抗性佝偻病的患者及六名对照受试者获取的活检材料来表征人空肠黏膜对无机磷酸盐摄取情况的尝试。对照受试者的组织以线性方式随时间积极积累³²P。无机磷酸盐掺入有机磷酸盐衍生物的过程迅速,在无机磷酸盐与总磷酸盐比例为0.45的情况下,10分钟后达到平衡。厌氧或氰化物均会抑制浓缩摄取和掺入。低磷血症患者组织对磷酸盐的摄取及掺入有机衍生物的速率与正常值相当。在广泛的底物浓度范围(0.003至3 mM)内观察到的饱和动力学仅引发一种转运系统,其表观米氏常数为0.2 mM,最大速度为0.7 mmol/升/40分钟。从患者获得的动力学数据与对照值并无显著差异。对两名患者和两名对照受试者的肠黏膜磷酸盐含量进行的化学分析表明,突变个体的组织并无特异性磷酸盐缺乏。这些结果与家族性低磷血症口服替代疗法所获得的阳性结果一致。