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在正常大鼠和氮质血症大鼠中,高磷血症在骨化三醇诱导的高钙血症期间适度延缓甲状旁腺激素的抑制。

Hyperphosphatemia modestly retards parathyroid hormone suppression during calcitriol-induced hypercalcemia in normal and azotemic rats.

作者信息

Jara Aquiles, Chacón Cecilia, Felsenfeld Arnold J

机构信息

Department of Nephrology, Pontificia Universidad Católica de Chile, Santiago, Chile.

出版信息

Nephron. 2002 Dec;92(4):883-8. doi: 10.1159/000065454.

Abstract

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.

METHODS

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.

RESULTS

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).

CONCLUSIONS

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.

摘要

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。

方法

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。

结果

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。

结论

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。

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