Ittel T H, Kluge R, Sieberth H G
Department of Internal Medicine II, RWTH, Aachen, FRG.
Nephrol Dial Transplant. 1988;3(5):617-23. doi: 10.1093/oxfordjournals.ndt.a091716.
The present study examines the time course of aluminium absorption in uraemic rats vs controls and investigates the effect of vitamin D. Following an oral load of 410 mumol aluminium there was a significant increase in the urinary excretion rate of aluminium as early as 60 min in uraemic rats. Compared with controls this increase was significantly greater in uraemic animals and maximum excretion rates (77 +/- 49 vs pre-load 2 +/- 1 nmol Al/h) were achieved after 2 h. When vitamin-D-deficient rats with normal renal function were compared with vitamin-D-replete controls, the latter excreted a significantly greater amount of the oral dose of aluminium in their urine (727 +/- 361 vs 359 +/- 140 nmol Al/5d; P less than 0.02) and the post-load increase in the serum aluminium concentration was more pronounced in the vitamin-D-replete animals. Aluminium administered i.v. resulted in similar urinary aluminium excretion rates in both groups. In uraemic rats, however, regardless of their vitamin D status, administration of 1,25(OH)2D3 had no effect on the amount of urinary aluminium excretion after oral or i.v. loads. These findings suggest that although in rats with normal renal function aluminium absorption appears to be partly vitamin D dependent, 1,25(OH)2D3 does not further augment the enhanced gastrointestinal absorption of aluminium in uraemia.
本研究检测了尿毒症大鼠与对照大鼠铝吸收的时间进程,并研究了维生素D的作用。给尿毒症大鼠口服410μmol铝负荷后,早在60分钟时铝的尿排泄率就显著增加。与对照相比,尿毒症动物的这种增加显著更大,2小时后达到最大排泄率(77±49对负荷前2±1nmol铝/小时)。当将肾功能正常的维生素D缺乏大鼠与维生素D充足的对照大鼠进行比较时,后者尿中排出的口服铝剂量显著更多(727±361对359±140nmol铝/5天;P<0.02),且负荷后血清铝浓度的增加在维生素D充足的动物中更明显。静脉注射铝后两组的尿铝排泄率相似。然而,在尿毒症大鼠中,无论其维生素D状态如何,口服或静脉注射负荷后给予1,25(OH)₂D₃对尿铝排泄量均无影响。这些发现表明,虽然在肾功能正常的大鼠中铝吸收似乎部分依赖维生素D,但1,25(OH)₂D₃并不会进一步增强尿毒症时胃肠道对铝的增强吸收。