Jara Aquiles, Chacón Cecilia, Felsenfeld Arnold J
Department of Nephrology, Pontificia Universidad Católica de Chile, Santiago, Chile.
Nephron. 2002 Dec;92(4):883-8. doi: 10.1159/000065454.
BACKGROUND/AIMS: In in vitro studies, a high phosphate concentration has been shown to directly stimulate parathyroid hormone (PTH) secretion in a normal calcium concentration and to reduce PTH suppression in a high calcium concentration. In hemodialysis patients during dialysis-induced hypercalcemia, the effect of hyperphosphatemia on PTH secretion was less than in vitro studies. Our goal was to determine whether hyperphosphatemia retards PTH suppression during calcitriol-induced hypercalcemia in azotemic rats with hyperparathyroidism.
Rats underwent a two-stage 5/6 nephrectomy or sham operations. After surgery, rats received a high phosphate diet (P 1.2%, Ca 0.6%) for 4 weeks to induce hyperparathyroidism and then were placed on a normal diet (P 0.6%, Ca 0.6%) for two additional weeks to normalize serum calcium values in azotemic rats. At week 7, rats were divided into five groups and before sacrifice received at 24-hour intervals, three doses of calcitriol (CTR) or its vehicle. The five groups and dietary phosphate content were: group 1--normal renal function (NRF) + 0.6% P + vehicle; group 2--NRF + 0.6% P + CTR; group 3--renal failure (RF) + 0.6% P + vehicle; group 4--RF + 1.2% P + CTR; and group 5--RF + 0.6% P + CTR.
In the two CTR-treated groups with marked hypercalcemia (groups 2 and 5), 15.52 +/- 0.26 and 15.12 +/- 0.13 mg/dl, respectively, stepwise regression showed that hyperphosphatemia retarded PTH suppression. When the two azotemic groups treated with CTR (groups 4 and 5) were combined to expand the range of serum calcium values, stepwise regression showed that hypercalcemia suppressed and hyperphosphatemia modestly retarded PTH suppression. Similarly, in groups 4 and 5 combined, correlations were present between PTH and both serum calcium (r = -0.70, p < 0.001) and serum phosphate (r = 0.64, p = 0.001).
Hypercalcemia and high doses of calcitriol markedly reduced PTH secretion in azotemic rats despite severe hyperphosphatemia. Even though hyperphosphatemia did retard PTH suppression during hypercalcemia, its effect was small.
背景/目的:在体外研究中,已表明高磷酸盐浓度在正常钙浓度下可直接刺激甲状旁腺激素(PTH)分泌,而在高钙浓度下可减少PTH的抑制作用。在血液透析患者发生透析诱导的高钙血症期间,高磷血症对PTH分泌的影响小于体外研究。我们的目标是确定在患有甲状旁腺功能亢进的氮质血症大鼠中,高磷血症是否会延缓骨化三醇诱导的高钙血症期间PTH的抑制作用。
大鼠接受两阶段5/6肾切除术或假手术。术后,大鼠接受高磷饮食(磷1.2%,钙0.6%)4周以诱导甲状旁腺功能亢进,然后再接受正常饮食(磷0.6%,钙0.6%)2周以使氮质血症大鼠的血清钙值正常化。在第7周时,将大鼠分为五组,在处死前每隔24小时给予三剂骨化三醇(CTR)或其赋形剂。五组及其饮食磷含量分别为:第1组——正常肾功能(NRF)+0.6%磷+赋形剂;第2组——NRF+0.6%磷+CTR;第3组——肾衰竭(RF)+0.6%磷+赋形剂;第4组——RF+1.2%磷+CTR;第5组——RF+0.6%磷+CTR。
在两个CTR治疗的伴有明显高钙血症的组(第2组和第5组)中,血清钙分别为15.52±0.26和15.12±0.13mg/dl,逐步回归显示高磷血症延缓了PTH的抑制作用。当将两个接受CTR治疗的氮质血症组(第4组和第5组)合并以扩大血清钙值范围时,逐步回归显示高钙血症抑制而高磷血症适度延缓了PTH的抑制作用。同样,在合并的第4组和第5组中,PTH与血清钙(r=-0.70,p<0.001)和血清磷(r=0.64,p=0.001)之间均存在相关性。
尽管存在严重的高磷血症,但高钙血症和高剂量的骨化三醇可显著降低氮质血症大鼠的PTH分泌。即使高磷血症在高钙血症期间确实延缓了PTH的抑制作用,但其作用较小。